Vector for efficient selection and/or maturation of an antibody and uses thereof

Abstract

It is described a vector suitable for efficient selection and/or maturation of a recombinant antibody characterized in that it contains at least one element able to reduce the expression level and/or has an improved efficiency of display of said recombinant antibody.

Description

CROSS REFERENCE TO RELATED APPLICATIONS

Two reissue applications have been filed for the reissue of U.S. Pat. No. 8,003,383: this application and a reissue continuation application, U.S. application Ser. No. 14/998,264 filed on Dec. 23, 2015. This application is a reissue of U.S. Pat. No. 8,003,383, which was filed as U.S. application Ser. No. 12/097,876 on Jun. 17, 2008, which, in turn, is the national phase of International Application PCT/IT2006/000876 filed on Dec. 27, 2006 which, in turn, claims priority to European Patent Application 05028501.4 filed on Dec. 27, 2005.

The present invention relates to a method of improving the antibody selection capacity in phage-display library, in which said improvement is obtained through the reduction of the expression levels of the antibodies produced in said library.

FIELD OF THE INVENTION

Recombinant DNA technology provides a cheap and useful alternative to monoclonal antibody production. Display of recombinant antibodies on bacteriophage capsid, known as phage-display, not only allows generation of human antibody libraries for selection of specific binders, providing antibodies useful for therapy not inducing a harmful immune response in patients, but also facilitates affinity maturation of antibodies through construction of mutant antibody libraries, giving clones with a higher affinity.

The possibility of finding high-affinity binders in a recombinant antibody library characterizes its quality, which depends on several factors like library size, diversity and source of immunoglobulin genes.

It is known that various lymphoid tissues from immunized or non-immunized donors, such as peripheral blood lymphocytes, spleen and bone marrow and even metastasized or drained lymph node tissue from individuals affected by tumors may serve as a source of specific antibody repertoire.

Although naïve antibody libraries are more diverse and lead to isolation of broad antibody specificities, it is reasonable to suggest that construction of a recombinant antibody library from Ig repertoire of a patient affected by specific disease can provide antibody fragments of higher binding affinity against particular antigens.

Several published studies describe construction of recombinant antibody libraries from tumor-associated lymph nodes (Clin. Exp. Immunol. 1997 109(1):166-74; Int. J. Mol. Med. 2004 14(4):729-35; World J. Gastroenterol. 2004 10(18):2619-23). These studies are based on the general idea that lymph node tissue from cancer patients are infiltrated with activated B cells, which may serve as source of tumor-specific antibodies.

It is quite difficult to obtain metastasized or drained lymph nodes from breast cancer patients as fresh surgical material. According to recent medical practice the surgeon removes only a sentinel lymph node or a small cluster of nodes (sentinel node and those closest to it), thus performing less invasive surgery and reducing side effects, instead of removing dozen of lymph nodes according to previous surgery technique. After sentinel lymph node dissection, practically the entire node is studied for presence of micrometastasis or single cancer cells. Therefore, in breast cancer surgery the metastasized node is practically unavailable as discarded surgical material.

The evidence that tumor-infiltrating B lymphocyte (TIL-B)-derived antibodies may also recognize tumor cells was obtained by producing human hybridomas, obtained from TIL, able to secrete tumor-specific antibodies (Lancet. 1982 1(8262):11-4; Br. J. Cancer, 1983 47(1):135-45); by B cell expansion of TIL from human tumor biopsies (Cancer Immunol. Immunother. 1994 38(4):225-32)_j by B cell expansion of melanoma-derived TIL and following cloning the scFv antibody from single B cell clone with specific melanoma reactivity (Cancer Res. 1995 55:3584-91); and by subcutaneous transplantation of human lung cancer tissue in immunodeficient mice producing human antibodies derived from TIL-B, which recognized two tumor-specific proteins (Cancer Invest. 2000; 18(6):530-6; Cancer Res. 2002 62(6):1751-6), thus suggesting a specific function of TIL-B in the tumor.

Recently, cervical carcinoma and a rare type of breast cancer, classified as medullary carcinoma (MCB) have been shown to be characterized by lymphoplasmacytic infiltrates that correlate with improved prognosis and patient survival. These diseases, were investigated to understand the nature of tumor-infiltrated B lymphocytes (TIL-B) by using also phage-display methods. Study of the molecular structure of variable antibody regions gave evidence of antigen-driven humoral immune responses in medullary breast carcinomas, as well as in cervical tumors. Oligoclonal predominance found in antibody genes derived from TIL indicated possible clonal selection of the Ig molecules against specific neoantigens overexpressed, or specifically expressed, in tumor tissue (Cancer Immunol. Immunother. 2001 50(10):523-32; Cancer Res. 2001 61(21):7889-99; Proc. Natl. Acad. Sci. U.S.A. 2001 98(22):12659-64; J. Immunol. 2002 169(5):2701-11).

Despite the very strong above-mentioned indications that tumor tissue is infiltrated with activated B cells, which may serve as a source of tumor-specific antibodies, several research groups, in the panning experiments performed with TIL-derived phage-display libraries against purified known tumor antigens, or living tumor cells, or frozen tissue sections, failed to select either a specific antibody discriminating between tumor and normal cells, or one reactive with cell-surface tumor antigens (Cancer Res. 2001 61(21):7889-99; Proc. Natl. Acad. Sci. U.S.A. 2001 98(22):12659-64; Int. J. Cancer 2001 93:832-40). Only later, two different groups managed to identify specific antibodies recognizing tumor cells from this kind of phage-display libraries (J. Immunol. 2002 169:1829-36; J Immunol. 2005 175(4):2278-85).

An alternative approach, based on a phage-expression tumor-derived library and direct plaque screening protocols, that avoided limitations of phage display system, allowed Wu and colleagues (Cancer Immunol Immunother. 2002 51(2): 79-90) to isolate multiple antibodies that specifically bound cultured tumor cells. This study indicates that the observed difficulties in selection of anti-tumor antibodies from TIL-derived phage-display libraries result from imperfection of display vectors known in the art. However, the direct screening is also not an excellent method for selection of recombinant antibodies from large libraries. Indeed it is a laborious procedure demanding large expenses of time and means, as compared to the phage display technology.

Applicant performed a screening of recombinant antibody phage-display libraries derived from TIL-B by utilizing novel phagemid vector pKM19 and demonstrated efficient selection of tumor-specific antibodies against desirable tumor antigens as well as against living breast carcinoma cells.

SUMMARY OF INVENTION

The authors have found that it is possible to improve the efficiency of selection and/or maturation of recombinant antibodies from libraries by using the phage-display system, upon suitable modifications of prior art vectors. Prior art vectors are, i.e., phagemid vectors as in “Antibody Engineering—A practical approach (McCafferty, J. Hoogenboom, H. & Chiswell D., eds), pp. 325, Oxford University Press, 1996)”.

Therefore it is an object of the instant invention a vector, suitable for efficient selection and/or maturation of a recombinant antibody, characterized in that it contains at least one element able to reduce the expression level and/or has an improved efficiency of display of said recombinant antibody.

In the instant invention a recombinant antibody includes: ScFv, active fragments of Abs, or any other derivatives of Abs known in the art, including humanized sequences of Abs.

The vector of the invention may be a plasmid, a phagemid, a phage, or any other vectors known to the skilled in the art.

In one preferred aspect the element able to reduce the expression level of the recombinant antibody belongs to the group of: a) a suppressed stop codon inside either the leader peptide or the antibody coding sequence; b) a low-efficient promoter driving transcription of said antibody coding sequence; c) an inhibitor of the promoter driving transcription of said antibody coding sequence.

Low-efficient promoters are known in the art and are exemplified in Biochem J. 1970 117: 741-746). Suitable inhibitors for promoters are known in the art and are exemplified in J. Bacteriol. 1979, 138(1):40-7.

In one preferred aspect the improved efficiency of display of said recombinant antibody is obtained by: a) fusing the recombinant, antibody coding sequence to a sequence coding for the carboxy-terminal part of the pIII protein; and/or b) using as leader peptide of the recombinant antibody the leader peptide of the alkaline phosphatase of E. coli; and/or c) eliminating any amber codon between the recombinant antibody coding sequence and the pIII coding sequence.

It is a further object of the present invention a phagemid vector having the nucleotide sequence of SEQ ID NO: 1.

This vector, named pKM19, is designed for the display of recombinant antibodies in single-chain format on the surface of filamentous phage.

It is a further object of the invention a phage display-antibody library obtained by cloning cDNAs into the vector of the invention. Preferably the library is obtained by cloning in the vector of the invention cDNAs from antibody producing cells, more preferably Tumor Infiltrating Lymphocytes (TILs) or Peripheral Blood Lymphocytes (PBLs). In a preferred aspect such antibody producing cells are isolated from a tumor affected subject, preferably from a breast cancer affected subject. Alternatively the library consists of synthetic or semi-synthetic antibody libraries, also mutated for affinity maturation of antibodies.

It is within the scope of the invention an antibody selected from the library of the invention, and method for selecting the same, able to recognize an antigen or a complex multi-component biological structure, preferably a cell or a cell membrane, more preferably selected from the group comprising: MUC1 tumor antigen, CEA (carcino-embrionic antigen), MCF7 breast carcinoma cells. Said antibodies may be in single or double-format.

In a particular aspect the MUC1 tumor antigen antibody is the MB5 scFv antibody consisting essentially of the amino acid sequence of SEQ ID NO: 3, preferably coded by the nucleotide sequence of SEQ ID NO: 2. Alternatively the MUC1 tumor antigen antibody is the MB5/C′1 scFv antibody, consisting essentially of the amino acid sequence of SEQ ID NO: 5, preferably coded by the nucleotide sequence of SEQ ID NO: 4. Alternatively the MUC1 tumor antigen antibody is the MB5/C′3 scFv antibody, consisting essentially of the amino acid sequence of SEQ ID NO: 7, preferably coded by the nucleotide sequence of SEQ ID NO: 6.

In a particular aspect the CEA tumor antigen antibody is the CB37 scFv antibody consisting essentially of the amino acid sequence of SEQ ID NO: 9, preferably coded by the nucleotide sequence of SEQ ID NO: 8. Alternatively the CEA tumor antigen antibody is the CB37/9C scFv antibody, consisting essentially of the amino acid sequence of SEQ ID NO:13, preferably coded by the nucleotide sequence of SEQ ID NO:12. Alternatively the MUC1 tumor antigen antibody is the CB37/3B scFv antibody, consisting essentially of the amino acid sequence of SEQ ID NO:11, preferably coded by the nucleotide sequence of SEQ ID NO:10.

In a particular aspect the MCF7 breast carcinoma cells antibody is the B96/11L scFv antibody consisting essentially of the amino acid sequence of SEQ ID NO: 15, preferably coded by the nucleotide sequence of SEQ ID NO: 14. Alternatively the MCF7 breast carcinoma cells antibody is the mix7 scFv antibody, consisting essentially of the amino acid sequence of SEQ ID NO: 17, preferably coded by the nucleotide sequence of SEQ ID NO: 16. Alternatively the MCF7 breast carcinoma cells antibody is the mix17 scFv antibody, consisting essentially of the amino acid sequence of SEQ ID NO: 19, preferably coded by the nucleotide sequence of SEQ ID NO: 18. Alternatively the MCF7 breast carcinoma cells antibody is the mix39 scFv antibody, consisting essentially of the amino acid sequence of SEQ ID NO: 21, preferably coded by the nucleotide sequence of SEQ ID NO: 20.

The antibodies selected from the libraries of the invention may be advantageously utilized for therapeutic, diagnostic, immunogenic or research purposes. Conveniently they may be utilized for preparing suitable pharmaceutical compositions comprising as active ingredient one or more recombinant antibody of the invention and optionally one or more excipients or diluents pharmaceutically acceptable and known in the art.

The antibodies of the invention may be also utilized for obtaining so-called maturation libraries wherein single Variable Heavy chains (VH) coding sequences are co-transfected with Variable Light chain (VL) coding sequences, and recombinant antibodies selected for affinity.

Moreover the antibodies may be utilized for selecting recombinant and/or synthetic peptides able to mimic the native antigen. Tumor surface antigens can be selected by using novel anti-tumor antibodies recognizing tumor cells through: (i) immunoprecipitation of unknown target proteins from tumor cell extracts (Antibodies. A laboratory manual. Ed Harlow, David Lane, Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press, 1988); or (ii) developing the immunoreactions with tumor cell extract, separated by two-dimensional PAGE (Proteins and proteomics: A laboratory manual. Richard J. Simpson, pp. 705, Science 2002) and transferred onto nitrocellulose membrane (Sambrook J, Fritsch E F, Maniatis T. Molecular cloning: A laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, 1989);

Such recombinant and/or synthetic peptides able to mimic the native antigen so obtained may be utilized for producing vaccines, diagnostic reagents or in the research field. Conveniently they may be utilized for preparing suitable pharmaceutical compositions comprising as active ingredient one or more disease-specific antigen above mentioned, and optionally one or more excipients or diluents pharmaceutically acceptable and known in the art.

It is a further object of the present invention a nucleic acid encoding for the recombinant antibody obtained by the library of the invention.

Preferably the nucleic acid encodes for a MUC1 tumor antigen antibody, more it has the nucleotide sequence of SEQ ID NO: 2. Alternatively it has the nucleotide sequence of SEQ ID NO: 4. Alternatively it has the nucleotide sequence of SEQ ID NO: 6.

Preferably the nucleic acid encodes for a CEA tumor antigen antibody, more preferably it has the nucleotide sequence of SEQ ID NO: 8. Alternatively it has the nucleotide sequence of SEQ ID NO: 10. Alternatively it has the nucleotide sequence of SEQ ID NO: 12.

Preferably the nucleic acid encodes for a MCF7 breast carcinoma cells antibody, more preferably it has the nucleotide sequence of SEQ ID NO: 14. Alternatively it has the nucleotide sequence of SEQ ID NO: 16. Alternatively it has the nucleotide sequence of SEQ ID NO: 18. Alternatively it has the nucleotide sequence of SEQ ID NO: 20.

It is a further object of the present invention a host cell transformed with the vector of the invention able to express the antibody.

It is another object of the invention a method for improving the selection and/or maturation of a recombinant antibody comprising the step of using as cloning and expression vector the vector of the invention as above described.

The invention will be now described by means of non limiting examples referring to the following figures:

DETAILED DESCRIPTION OF THE DRAWINGS

FIG. 1. It is schematically described the essential elements of pKM16 plasmid useful for the production of soluble antibodies in scFv format and the essential elements of pKM17, pKM18 and pKM19 plasmids useful for production of phage-displayed antibodies. These plasmids direct antibody expression under control of pLac promoter. The unique NcoI and NotI cloning sites allow insertion of an antibody gene to express single-chain antibodies with a leader peptide of the bacterial periplasmic enzyme, alkaline phosphatase (PhoA leader). Plasmid pKM17 encodes the entire protein pIII (406 aa) and plasmids pKM18 and pKM19 encode the carboxy-terminal part of pIII (197 aa). Plasmid pKM19 contains amber codon in PhoA leader.

FIGS. 2a, 2b, 2c. It is described the detailed structure of pKM19 phagemid vector (SEQ ID NO: 1). The specific modification made are reported in the figure and described in the text.

FIG. 3. Soluble scFv production by using pKM16 plasmid. Three independent clones obtained by cloning scFv anticarcino-embryonic antigen (CEA) gene in pKM16 were tested for soluble scFv production (gel lines 1-3). Periplasmic protein fractions were purified from bacteria by freeze and thaw method. The protein size marker is included. Western blot membrane was developed with an anti-FLAG AP-conjugated secondary antibody. Bands corresponding to soluble scFv antibodies (expected molecular weight 26 kDa) migrate between 24.5 and 35.9 kDa bands.

FIG. 4. Display efficiency of pKM17, pKM18 and pKM19 plasmids in comparison with a classic phagemid system. Anti-CEA scFv antibodies displayed by the three different plasmids, were assayed by ELISA against CEA protein and compared with MA39 phage (anti-CEA/pDN322). The helper phage, M13K07, that does not display antibody fragments, was included as negative control. Data reported are the average values of assays performed in duplicate. The highest phage concentration, labeled by asterisk, corresponds to the 10¹¹ TU for all phages and 3×10¹⁰ TU for anti-CEA/pKM17. The ELISA was performed by using the anti-M13 (panel A), or alternatively, the anti-FLAG secondary antibody (panel B).

FIG. 5. Filtration of phage samples. About 2×10¹¹ TU/well of each preparation or the corresponding quantity of filtrate samples were tested in ELISA and developed either with anti-M13 (panel A) or anti-FLAG (panel B) secondary antibodies. Data reported are the average values of assays performed in duplicate. The data show reactivity of filtrates against CEA as percentage of original reactivity of non-filtrated samples (100%).

FIG. 6. Competition with soluble anti-CEA scFv. Freshly prepared supernatants of MA39 (10 μL) and anti-CEA/pKM19 (5 μL) phages competed with various amounts of the purified soluble anti-CEA antibody. The data are expressed as percentage of reactivity of the supernatants without competitors. The irrelevant soluble anti-SP2 scFv was used as negative control.

FIG. 7. Competition with phage supernatant filtrates. Freshly prepared supernatants of MA39 (10 μL) and anti-CEA/pKM19 (5 μL) phages were competed with 10 μL or 50 μL of filtrates of the same phage supernatants. The data are expressed as percentage of reactivity of the supernatants without competitors.

FIG. 8. Western blot of PEG-purified recombinant phages. Protein extracts from about 5×10⁹ PFU of phages MA39, anti-CEA/pKM18 and anti-CEA/pKM19, and 1×10⁹ PFU of anti-CEA/pKM17 were fractionated by SDS-PAGE and transferred onto a nitrocellulose membrane. The membrane strips were developed with an anti-FLAG AP-conjugated antibody. The protein size marker is included (last strip). The scFv-pIII (66.1 kDa) and scFv-ΔpIII (45.2 kDa) proteins migrate as higher molecular weight bands because of an anomalous moiety of the pIII protein described earlier (Goldsmith and Konigsberg, 1977).

FIG. 9. Selection against SP2-GST protein. Reactivity of the phage pools derived from first and second rounds of panning of the scFvEC23 library is shown. GST (glutathione S-transferase), milk and streptavidin, present in the selection system, are included as negative controls. Data reported are the average values of assays performed in duplicate. Phage input was normalized since 3×10⁹ TU per single well of each preparation were tested in ELISA.

FIG. 10 Affinity selection of maturated anti-CEA gene from a maturation library. In this assay, positive immunoreactions were developed by an anti-FLAG AP-conjugated secondary antibody, in order to moderate positive signals and make visible the increasing reactivity during the selection process. The helper phage, M13K07, that does not display antibody fragments, was included as negative control. The reactivity of the original anti-CEA antibody in pKM19 (anti-CEA/pKM19), maturation library (Lib.), pools of phage after first and second round of selection (I round, II round) and single clones (c1.1, c1.2) from the phage pool after second round of affinity selection, tested on CEA and irrelevant GST protein, are shown. Data reported are the average values of assays performed in duplicate. Phage input was normalized. About 3×10¹⁰ TU per single well of each preparation were tested in ELISA.

FIG. 11. ELISA reactivity of soluble maturated scFvs. Various amounts of soluble antibodies were assayed on CEA-coated plates. Bound scFvs were developed by using an anti-FLAG secondary antibody. Data reported are the average values of assays performed in duplicate. The irrelevant anti-SP2 antibody and maturated anti-CEA ES antibody, obtained earlier (Pavoni et al., 2006), were included as controls.

FIG. 12. Specificity of maturated clones. About 250 ng per well of original and maturated antibodies in soluble form were assayed with CEA and various irrelevant proteins. The irrelevant anti-SP2 antibody was included as negative control. Data reported are the average values of assays performed in duplicate.

FIG. 13. V(D)J analysis of TIL-derived antibody genes. A. SMART cDNAs derived from 10 different tumor samples (patients B84, B85, B87, B89, B90, B91, B92, B93, B95, B96), from normal breast, normal testis and lymphocytes from four healthy donors (L1, L2, L3, L4), were used, as template for amplification of V(D)J antibody regions. Samples of the cDNAs were normalized by amplification of β-actin housekeeping gene. V(D)J fragments were amplified well from all templates excluding normal testis cDNA. B. The same PCR products were fractionated by PAGE giving a higher resolution for DNA bands.

FIG. 14. Antibody subclass distributions. PCR-amplified normal breast and B84 cDNA samples, not showing oligoclonal bands in the V(D)J test, have prevalence of IgA bands in comparison to IgG1 and IgG2 (left panel), while three samples, showing strong oligoclonal bands in previous test (B91, B92 and B93), have IgG1 or both IgG1 and IgG2 bands prevalence in comparison with IgA (right panel).

FIG. 15. Amino acid sequences of variable regions of 30 random clones obtained by cloning γ-chain antibody genes derived from B92 (SEQ ID NO: 54 to SEQ ID NO:64) and B93 (SEQ ID NO: 65 to SEQ ID NO: 77) cDNAs. Peptide sequence is reported in single-letter code. Identical amino acids a in similar clones are represented by a dash.

FIG. 16. Selection on ED-B, MUC1 and CEA proteins. Reactivity of phage pools derived from second and third rounds of panning in comparison with original libraries were tested. GST is included as a negative control. Additional negative control, protein D possessing 6His tail as a target protein used in the selection was used in case of ED-B panning. Data reported are the average values of assays performed in duplicate. Library ScFvEC23 derives from PBL. MixTIL is a mixture of 4 TIL-derived libraries (ScFvB87, ScFvB95, ScFvB96 and ScFvmix) as indicated in table 1.

FIG. 17. ELISA reactivity of single phage clones displayed scFv antibodies. Reactivity of single phage clones selected against ED-B (clones EDE1, EDE3, EDE5, EDB5, table 5), MUC1 (clones ME 1, ME2, MB5, table 5) and CEA (clones CB3, CB37, CB40, CB41, CB53, CB60, table 5) after third round of selection was tested using respective proteins. Data reported are the average values of assays performed in duplicate. Several irrelevant proteins and an anti-SP2 irrelevant phage antibody are included as negative controls.

FIG. 18. Cell-based panning reactivity against fixed breast carcinoma (MCF7) and human fibroblast (HFF) cells of phage pools derived from fourth and fifth rounds of panning in comparison with original libraries, were tested. Data reported are the average values of assays performed in triplicate. Libraries scFvB96 and mixLIB are defined in Table 2.

FIG. 19. Cell-ELISA reactivity against fixed cells of single phage clones. Data reported are the average values of assays performed in triplicate. Cell developing with irrelevant anti-SP2 antibody is included as negative control. MCF7 and MDA-MB-468: fixed breast carcinoma cells; HFF: human fibroblast and MCF10-2A: normal breast epithelium cells.

FIG. 20. Origin of anti-MCF7 scFv antibodies. One μL of each scFv phage library was amplified by PCR by using oligonucleotide primers specific for analyzed antibody genes. Corresponding PEG-purified phage was used as positive control (last line). The irrelevant anti-SP2 antibody gene of known origin, selected earlier from scFvEC23 library; derived from PBL, was also tested. Anti-MUC1 MB5 antibody and anti-CEA CB37 antibody were selected from mixture of TIL-derived libraries. Mix 11, mix 12, mix17 and mix39 antibodies were selected from mixture of TIL-derived and PBL-derived libraries Antibodies are defined in Table 5.

FIG. 21. Fluorescent staining of non-permealized breast carcinoma MCF7 and normal breast epithelium MCF10-2A fixed cells by phage-displayed scFv antibodies (mix17 (A), mix7 (B)).

FIG. 22. A. Fluorescent staining of breast carcinoma cells MCF7, SkBr3 expressing MUC1 tumor antigen and normal breast epithelium cells MCF 10-2A by using phage-displayed anti-MUC1 MB5 scFv antibody; B. Staining of colorectal adenocarcinoma cells LoVo expressing CEA by phage-displayed anti-CEA CB37 scFv antibody. Staining of negative control MCF10-2A cells is included.

The following examples illustrates the invention.

Example 1

Construction of Novel pKM19 Phagemid Vector for Display of Single-Chain Antibodies on Filamentous Phage

Introduction

This work describes construction of a novel pKM19 phagemid vector for the display of single-chain antibodies on filamentous phage. This vector is characterized by several differences compared to canonical systems.

a) Amber Codon

The classic phagemids contain an amber codon between the scFv and gpIII genes, thus directing production of free scFvs and scFv-pIII fusion antibodies in suppressor bacteria, such as TG1, or DH5αF′, or XL1-Blue, generally used for phage amplification. These bacterial strains, carrying the supE mutation, are glutamine-inserting suppressors with suppression efficiency dependent on the codon following the TAG (J. Mol. Biol. 1983 164(1):59-71; Mol. Gen. Genet. 1987 207(2-3):517-518). In such system, the produced free soluble scFv antibodies are secreted into the periplasm and then leak from the periplasm into the medium. Under standard phage purification protocol by PEG/NaCl, the free scFv antibodies are co-precipitated with phage particles. As a result, the concentration of free antibodies in phage suspension may be five to ten times higher than the concentration of scFv-pIII-fused proteins assembled in the phage particle. In a subsequent selection, the abundant free antibodies compete with phage-displayed antibodies for target binding. This interferes with panning efficiency and delays the selection process, specially:

i) when antigen concentration is limited (e.g. biopanning on living cells, ex-vivo cells),

ii) in later panning rounds, where concentration of specific phage is relatively high, or

iii) in maturation libraries, containing many relative antibodies with the same specificity.

Therefore classic phagemids need to be modified for an improved selection and/or maturation of antibodies.

As expected from literature data, the presence of an amber codon positioned in a sequence encoding for a phosphatase alkaline leader peptide in pKM19, leads to a relatively low expression level of recombinant antibodies in the amber-suppressor bacteria harboring this plasmid.

It was shown (Gene 1999 228: 23-31) that inhibition of lac promoter only by catabolic repression with glucose is not sufficient to equilibrate growth rates of different clones with or without stop codons. The lower scFv expression achieved using pKM49, reduces the toxicity of recombinant antibodies for the bacterial host and has no influence on display efficacy.

Using pKM19 the authors demonstrated:

(i) that the present level of antibody expression is sufficient to produce highly reactive phage antibodies, giving a similar signal in ELISA test as compared to pKM18 phage without amber codon;

(ii) that specific antibodies can be easily isolated from an scFv library constructed from peripheral blood lymphocytes of a patient with antibodies against a target protein after only two selection rounds;

(iii) that maturation of anti-CEA antibody leads to isolation of improved scFv clones without stop codons in comparison with maturation performed by using canonical vector (BMC Cancer 2006 6:41).

b) Gene III Protein

The pKM19 vector allows the cloning of scFv fragments as amino terminal fusion of the deleted gene III protein.

Commonly used phage display vectors for scFv lead to incorporation into the phage particles of the entire pIII fused to the antibody fragment (in Antibody Engineering—A practical approach: McCafferty, J. Hoogenboom, H. & Chiswell D., eds, pp. 325, Oxford University Press, 1996), while in the case of pComb3 plasmid utilized for Fab display (Proc. Natl. Acad. Sci. USA 1991 88(18):7978-7982), the antibody fragment is fused to the carboxy terminal half of the pIII. Infectivity of such recombinant phages is obtained during their propagation, since superinfection with a helper phage provides the native gene III protein.

According to the present data, fusion of the single-chain antibody to the C-terminal part of pIII improves phage production and display efficiency of an antibody in comparison with wt pIII protein fusion. These data are in agreement with Kretzschmar's earlier data (Gene 1995 155(1):61-65). The improved display efficiency in combination with elimination of free scFv antibodies from the incubation mixture facilitates affinity selection and results in faster enrichment of the phage pools for specific clones. This may also contribute to reduction of stop codons in selected clones since a lower number of panning/amplification rounds are necessary to complete selection. Rapidly growing defective clones have less chance of being isolated.

c) PhoA Leader Peptide

In bacteria harboring the pKM19 vector, after synthesis of recombinant protein, the PhoA leader peptide is cleaved off by leader peptidase upon membrane translocation, and scFv-pIII is assembled into the phage particle. In this way, the entire cleavage site of the alkaline phosphatase, a genuine periplasmic protein of E. coli, is preserved to guarantee efficient and correct processing and antibody assembly. As a result, the mature protein contains two additional amino acids at the N-terminus of scFv. In the described system, it is necessary to reclone the antibody gene in the appropriate plasmid for the subsequent production of soluble antibodies. At this stage, the additional amino acids can be conserved or eliminated according to specific requirements.

In conclusion, the combination of relatively low expression of displayed antibodies by introducing the amber codon before antibody gene with improved display efficiency makes the novel pKM19 phagemid useful both for selection of the recombinant scFv antibodies against desired targets from large libraries, as for their affinity maturation. The plasmid guarantees efficient display and allows reduction of biological bias against “difficult” antibodies in the delicate initial selection step. Moreover, this vector is particularly useful for the affinity maturation of antibodies, since high expression levels may increase avidity of phage particles displaying Ab, leading to selection of antibodies with only modest affinity.

Methods

Bacterial Strains and Phages

Bacterial strain DH5αF′ (supE44 ΔlacU169 (100 lacZΔM15) hsdR17 recA1 endA1 gyrA96 thi-1 re1A1 F′ [traD36 proAB⁺ lacI^qlacZΔM15]) was used for soluble and phage antibody production. Helper phage M13 KO7 (Sambrook J, Fritsch E F, Maniatis T. Molecular cloning: A laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, 1989) was used for phage preparation.

The anti-CEA phage antibody, MA39 (BMC Cancer 2006 6: 41), in pDN322 plasmid (J. Biol. Chem. 1998 273(34): 21169-21776) was used as source of anti-CEA antibody gene.

Construction of Plasmids

The pC89 plasmid (J. Mol. Biol. 1991 222(2): 301-310) was amplified by inverse PCR with the KM161, I(M162 oligonucleotides, containing HindIII and NotI sites (underlined) (KM161 5′-GAGG AAGCTTCCATTAAACGGGTAAAATAC-3′ (SEQ ID 78); KM162 5′-TGCAATG GCGGCCGCTAATATTGTTCTGGATATTACCAGC-3′ [SEQ ID 79]). In inverse PCR a Taq polymerase mixture with Pfu DNA polymerase was used to increase fidelity of DNA synthesis. Twenty-five cycles of amplification (95° C.-30 sec, 55° C.-30 sec, 72° C.-20 min) were done. The PCR product was digested with HindIII and NotI endonucleases and ligated with a KM163-KM164 oligonucleotide duplex encoding FLAG peptide and His-tail (KM163 5′-AGCTTCCTC ATG TAG GCG GCC GCA GGA GAC TAC AAA GAC GAC GAC GAC AAA CAC CAC CAT CAC CAC CAT TAA-3′ [SEQ ID 80]; KM164 5′-GGCC TTA ATG GTG GTG ATG GTG GTG TTT GTC GTC GTC GTC TTT GTA GTC TCC TGC GGC CGC CTA CAT GAGGA-3′ [SEQ ID 81]). The cloned DNA duplex contained an internal NotI site, upstream of FLAG peptide encoding sequence, while the NotI site, used for cloning of the duplex, was not restored. The resulting pKM15 plasmid was newly digested with HindIII, NotI endonucleases and ligated with KM175-KM176 duplex encoding the leader sequence and the first two amino acids of the PhoA bacterial protein, containing the NcoI cloning site (KM175 5′-AGC TTA TAA AGG AGG AAA TCC TCA TGA AAC AGA GCA CCA TCG CAC TGG CAC TGT TAC CGT TAC TGT TCA CCC CGG TTA CCA AAG CAC GTA CCA TGG TTT CCC TTGC-3′ [SEQ ID 82]; KM176 5′-GGC CGC AAG GGA AAC CAT GGT ACG TGC TTT GGT AAC CGG GGT GAA CAG TAA CGG TAA CAG TGC CAG TGC GAT GGT GCT CTG TTT CAT GAG GAT TTC CTC CTT TATA-3′ [SEQ ID 83]). This new pKM16 plasmid was destined for soluble single-chain antibody production (FIG. 1).

The plasmid pKM16 was amplified by inverse PCR with the KM181, KM182 oligonucleotides, presenting EcoRI and BamHI restriction sites, respectively (KM181 5′-GTG GTG ATG GAATTC TTT GTC GTC GTC GTC TTT GTA GTC-3′ [SEQ ID 84]; KM182 5′-CAC CAT TAA GGATCC TAA TAT TGT TCT GGA TAT TAC CAG C-3′ [SEQ ID 85]). The full-length gene III (Accession number V00604) and the 3′ part of the gene encoding the last 197 aa of the pIII were amplified by using the oligonucleotides KM183-KM185 or KM184-KM185 containing BamHI and EcoRI sites (underlined) and ligated into digested pKM16, giving the new plasmids pKM17 and pKM18, respectively (KM183 5′-TC TAT TCT GAATTC GCT GAA ACT GTT GAA AGT TGT TTA GC-3′ [SEQ ID 86]; KM184 5′-GC CAA TCG GAA TTC CTG CCT CAA CCT CCT GTC AAT GCT-3′ [SEQ ID 87]; KM185 5′-GAA CTG GGA TCC TTA AGA CTC CTT ATT ACG CAG TAT G-3′ [SEQ ID 88]).

A short fragment of the pKM18 plasmid encoding the leader sequence was PCR-amplified with KM186-KM180 primers, introducing an amber mutation in PhoA leader peptide gene (KM186 5′-ACC CGT AAG CTT ATA AAG GAG GAA ATC CTC ATG AAA TAG AGC ACC ATC GC-3′ [SEQ ID 89]; KM180 5′-TAG CCC CCT TAT TAG CGT TTG-3′ [SEQ ID 90]). The resulting PCR product was digested with HindIII and NotI and cloned into pKM18, digested with HindIII and NotI and purified from agarose, to construct the pKM19 plasmid.

Soluble Antibody Production

A single colony was inoculated into 50 mL of LB containing 100 μg/mL Ap and 2% glucose. The culture was grown at 37° C. for 2-3 h up to O.D.=0.8. The cells recovered by centrifugation were resuspended in 50 mL of LB with Ap and 1 mM IPTG and incubated overnight at 30-32° C. Cell pellet was resuspended in 500 μL of PBS. After three cycles of freeze and thaw, cell debris was pelleted by centrifugation. The resulting supernatant was used for ELISA or for Western blot.

Purification of Lymphocytes from Peripheral Blood and cDNA Synthesis

The lymphocytes were isolated from 10 mL of fresh peripheral blood from patient EC23 (with advanced stage of breast cancer) with an anticoagulant using Ficoll-Paque Plus (Amersham Pharmacia Biotech, Sweden) according to manufacturer's instructions. mRNA was isolated from lymphocytes by using Dynabeads mRNA DIRECT Kit (Dynal, Norway). The mRNA was isolated from lymphocytes by using Dynabeads mRNA DIRECT Kit (Dynal, Oslo, Norway). One μg of the poly(A)⁺ RNA from the lymphocytes was used to synthesize full-length cDNA by using SMART cDNA Library Construction Kit (Clontech, Palo Alto, Calif.).

ScFv Library Construction

The antibody gene repertoire was amplified using a set of primers designed for amplification of VH and VL antibody domains, while entire scFv fragments were assembled in vitro as it was described in [Pope, A. R., Embleton, M. J. & Mernaugh R. (1996) Construction and use of antibody gene repertoires. In: Antibody Engineering—A practical approach (McCafferty, J., Hoogenboom, H. & Chiswell D., eds), pp. 325, Oxford University Press]. The latter were then amplified by PCR with appropriate extension primers, incorporating NcoI, NotI restriction sites, and allowing the cloning of scFv genes into a pKM19 vector. The resulting PCR products were purified on 1% low-melting agarose gel (NuSieve 3:1 agarose, Rockland, Me.), cut with NcoI/NotI and inserted into digested plasmid. The transformed library scFvEC23 contained 1.77×10⁷ independent clones with full-length scFv insert. The scFvEC23 library derives from PBL obtained from a single patient EC23 with advanced stage of breast cancer.

Construction of Mutated Anti-CEA scFv Library

The maturation library for the anti-CEA scFv was constructed as earlier described (BMC Cancer 2006 6:41). Briefly, mutated scFv gene fragments were generated by PCR amplification with primers: KM144-KM143 (KM143, 5′-GTCATCGTCGGAATCGTCATCTGC-3′ [SEQ ID 91]; KM144, 5′-TGTGCGAAA AGTAATGAGTTTCTTTTTGACTACTGGGGC-3′ [SEQ ID 92]) and KM148-KM145 (KM148, 5′-CTATTGCCTACGGCAGCCGCTGGA-3′ [SEQ ID 93]; KM145, 5′-TCCGCCGAATACCAC ATAGGGCAACCACGGATAAGAGGAGTTACAGTAATAGT CAGCC-3′ [SEQ ID 94]) introducing random mutations in CDR3 regions of heavy or light chains with low frequency. Each underlined base of KM144 and KM145 oligonucleotides was replaced with mixture of G/A/T/C with a frequency of 10%. Missing scFv antibody gene parts were amplified with KM148-KM157 and KM158-KM143 primers for HC and LC, respectively (KM157 5′-TTT CGC ACA GTA ATA TAC GG-3′ [SEQ ID 95]; KM158 5′-TAT GTG GTA TTC GGC GGA-3′ [SEQ ID 96]). In order to reconstruct the entire gene, the corresponding fragments were combined and amplified in a PCR-like process without oligonucleotide primers. The resulting product was utilized to amplify the entire gene with external primers KM148, KM143. The final DNA fragment was agarose-purified, digested with restriction enzymes NcoI and NotI, and ligated with the digested plasmid pKM19. The resulting library contained 2.2×10⁶ mutated antibody clones.

Competition with Soluble scFv

ELISA plates were coated, blocked and washed as above. Various quantities of anti-CEA soluble antibody MA39 (BMC Cancer 2006 6: 41) in 100 μL of blocking buffer were added to the wells and incubated for 30 min at 37° C. Then, 10 μL (4.5×10⁹ TU) of MA39 phage supernatant or 5 μL (3×10⁸ TU) of anti-CEA/pKM19 supernatant were added to the wells and incubated for another 1 h at 37° C. The plates were washed and the bound phage detected by an anti-M13 HRP-conjugated antibody. An irrelevant soluble anti-SP2 scFv (Table 5), was used at a high concentration (400 ng/well) as negative control. A lower quantity of the anti-CEA/pKM19 phage, as compared to MA39, was used to moderate ELISA reactivity of this phage.

In the case of competition with filtrates of phage supernatants, 10 μL or 50 μL of the MA39 or pKM19/anti-CEA filtrates in 100 μL of blocking buffer were used as competitors. The phage filtrates were obtained from freshly prepared phage supernatant by using filtration column Microcon 100.

Western Blot of PEG-Purified Phages

Phage was purified according to standard PEG/NaCl precipitation (Sambrook J, Fritsch E F, Maniatis T. Molecular cloning: A laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, 1989). Protein extracts from phage samples were fractionated by SDS-PAGE and transferred onto a nitrocellulose membrane. The membrane strips were developed with an anti-FLAG AP-conjugated antibody.

Phage ELISA

Multiwell plates (Immunoplate Maxisorb, Nunc, Roskilde, Denmark) were coated ON at 4° C. with a protein solution at a concentration of 10 mg/mL in 50 mM NaHCO3, pH 9.6. After discarding coating solution, plates were blocked for 1 h at 37° C. with ELISA blocking buffer (5% non-fat dry milk, 0.05% Tween-20 in PBS). Plates were washed several times with washing buffer (0.05% Tween-20 in PBS). PEG-purified phage in blocking buffer (1:1) was added to each well and incubated for 1 h at 37° C. The plates were washed and the bound phage was detected by an anti-M13 HRP-conjugated (27-9421-01, Amersham Biosciences, Uppsala, Sweden), or anti-FLAG HRP-conjugated (A9044, Sigma, St. Louis, Mo.), or anti-FLAG AP-conjugated (A9469, Sigma) secondary antibody. In the case of HRP-conjugates, the immunoreaction was developed by incubation with TMB liquid substrate (Sigma) for 15 min and stopped by the addition of 25 μL 2 M H₂SO₄. The results were expressed as the difference between absorbances at 450 and 620 nm, determined by an automated ELISA reader. The AP-conjugated antibody was detected by incubation with 1 mg/mL solution of p-nitrophenyl phosphate in substrate buffer (10% diethanolamine buffer, 0.5 mM MgCl2, pH 9.8) for 60 min. The results were expressed as the difference between absorbances at 405 and 620 nm.

Antibodies are defined in table 5.

Results

The pKM16 plasmid (FIG. 1) used for production of soluble antibodies in scFv configuration is constructed as described above. This plasmid directs protein expression under the control of lacP promoter. The unique NcoI and NotI cloning sites allow insertion of an antibody gene able to express single-chain antibodies with a leader peptide of the bacterial periplasmic enzyme, alkaline phosphatase (AP), and with the first two amino acids of the mature AP protein, at the antibody's amino-terminus; and FLAG/His-tail at carboxyl-terminus of antibody. In order to confirm the plasmid's practical qualities, a gene of a single-chain antibody of known specificity, the anti-CEA MA39, was amplified by PCR and cloned into the pKM16 vector. The authors then analyzed freeze-thaw purified periplasmic proteins in Western blot developed with an anti-FLAG secondary antibody (FIG. 3). Single-chain antibody bands migrated as proteins with the expected molecular weight. N-terminal protein sequencing by Edman degradation confirms the correct processing of the leader peptide.

Phagemids for Display of scFv Antibody

A classic phagemid (pDN322) displaying the anti-CEA single-chain antibody, MA39, was compared with pKM17, pKM18 and pKM19 vectors displaying the same antibody, for phage particle production and display efficiency. The pKM17 and pKM18 plasmids (FIG. 1) allow display of antibody fragments on a phage particle by fusion to, respectively, the entire pIII (1-406 aa) or the carboxy terminal domain only (210-406 aa) of the protein. The pKM19 plasmid, derivative of pKM18, harbors an amber codon in leader sequence, thus leading to lower production of scFv-pIII fusion proteins as compared to pKM18. This is in agreement with data showing that in supE bacteria, suppression efficiency of this TAG codon, which depends on nucleotide context, is about 10-15% (J. Mol. Biol. 1983 164(1): 59-71; Mol. Gen. Genet. 1987 207(2-3): 517-518).

The authors performed functional tests by cloning the anti-CEA single-chain antibody gene into the three novel plasmids and confronting them with the original MA39 clone (anti-CEA in pDN322).

Three single colonies for each clone were incubated in 10 mL of media and phage was amplified as described in Example 2. After phagemid rescue the supernatants were titered. The authors obtained a range between 5 to 1×10¹¹ TU/mL for MA39, pKM18 and pKM19, displaying the anti-CEA antibody, while anti-CEA/pKM17 generated five to ten times lower titers (Table 1).

TABLE 1
Phage production by different phagemid vectors
encoding the same anti-CEA gene.
Phage	Clone	Titer	Phage	Clone	Titer
MA39	1	1.5 × 1011	anti-	1	2.52 × 1011
			CEA/pKM18
	2	2.55 × 1011		2	2.5 × 1011
	3	5.1 × 1011		3	1.75 × 1011
anti-	1	6 × 1010	anti-	1	3 × 1011
CEA/pKM17			CEA/pKM19
	2	4.1 × 1010		2	1.8 × 1011
	3	1.95 × 1010		3	2.8 × 1011

Phage preparations were tested in ELISA, where developing was performed by using the anti-M13, or alternatively, the anti-FLAG secondary antibody. Applying different amounts of the phage per ELISA well, the authors demonstrated higher display efficiency for pKM18 and pKM19 phages in comparison with pKM17 and much higher as compared to MA39 (FIG. 4). It is interesting that the MA39 clone, which produces a higher level of antibodies than anti-CEA/pKM17, as shown by developing with anti-FLAG antibody (FIG. 4B), has a weaker signal when ELISA is developed with the anti-M13 secondary antibody (FIG. 4A).

This indicates that free scFvs, produced by the classic phagemid system, leak into the medium and coprecipitate with phage particles, consequently competing with phage-displayed antibodies for target binding. This phenomenon is due to the presence of an amber codon between scFv and pIII genes.

In order to verify this hypothesis, the authors filtered fresh preparations of MA39 and anti-CEA/pKM19 phage by using Microcon 100 Centrifugal Filter Devices (Millipore Corporation, Bedford, Mass.), able to retain large phage particles and pass through soluble scFvs. The ELISA test of phage preparations, before and after filtration, developed with anti-M13 or anti-FLAG antibodies, shows that:

(i) filtrates from both MA39 and pKM19 practically lose antibodies displayed on the phage particles, as expected;

(ii) the free antibodies are present in both preparations (FIG. 5).

However, the level of free antibodies in the anti-CEA/pKM19 sample is markedly lower. The free antibodies in this sample are the result of antibody shedding, inevitable during phage preparation and which might increase as a result of contact with components of the filtration system; while the free antibodies in MA39 samples are the result of free antibody expression and leakage into medium together with shedding.

To test the competitive ability of free antibodies in phage supernatants we had the phage supernatants of the MA39 and anti-CEA/pKM19 phages compete either with the soluble anti-CEA antibody of known concentration (FIG. 6) or with different quantities of supernatant filtrates of both phages (FIG. 7). These two experiments show that the free scFvs efficiently compete with the phage antibodies. Ten μL of the MA39 filtrate already competes with 10 μL of its own phage supernatant and 5 μL of anti-CEA/pKM19 supernanant, while the same quantity of anti-CEA/pKM19 filtrate has no effect. Marked competition is observed only by a ten-fold excess of anti-CEA/pKM19 filtrate with the same phage supernatant (50 μL of filtrate to 5 μL of supernatant). Western blot analysis (FIG. 8) of various PEG-purified phages developed with an anti-FLAG antibody detects: (i) the upper band in each sample corresponding to scFv-pIII fusion in case of MA39 and anti-CEA/pKM17 phages, and scFv-ΔpIII in case of anti-CEA/pKM18 or anti-CEA/pKM19; (ii) a notable presence of free antibodies in MA39 sample; (iii) presence of degradation products in the phage samples as previously described (Gene 1995 155(1):61-65).

Generation of scFv Antibody-Displayed Library and Isolation of Binding Specificities Using New pKM19 Plasmid

The pKM19 plasmid, a derivative of pKM18, harboring amber codon in leader sequence was used for generation of scFv library to study whether low production of fused antibodies allows efficient selection of a specific antibody against a target molecule.

An scFv antibody library was constructed from human peripheral blood lymphocytes as described in Materials and Methods. The library was selected against GST fusion of a 168 aa-long SP2 Streptoccocus pneumoniae polypeptide (FEMS Microbiol. Lett. 2006 262(1):14-21), which was reactive with the blood sample utilized for the scFv library construction.

A selection procedure was designed to create a high concentration of the target protein in small incubation volume, by using biotinylated protein for panning and streptavidin-coated Dynabeads for isolation of bound phage, as described in Example 2. After completion of two panning rounds, we tested the reactivity of the phage pools in ELISA (FIG. 9). The phage pool, after the second round of affinity selection, was highly reactive with the fusion protein and negative with irrelevant proteins, such as GST, milk and streptavidin, which presented either as protein carrier or components of the selection system and all used as negative controls in ELISA, thus indicating successive selection of specific antibodies.

Finally, the authors isolated and sequenced a number of positive clones to confirm correct scFv sequence. One of the identified scFv genes was cloned in pKM16 for production of soluble anti-SP2 antibody (Table 5), which was used as an irrelevant antibody control in experiments described in FIGS. 6, 11 and 12.

Maturation of Anti-CEA scFv Antibody by Using pKM19 Vector

Affinity selection from a maturation library was carried out as described in BMC Cancer 2006 6:41. FIG. 10 shows that phage reactivity against the CEA protein grows in each successive selection round. Single phage clones with improved reactivity were isolated (FIG. 10). The authors sequenced 19 random clones from the phage pool after the second round of selection. None of the phage pool sequenced clones having increased affinity (0 of 19) presented stop codons in their sequence, whereas 70% (9 of 13) of classic phagemid system clones contained such mutations (P=0.00002, calculated according to chi square test). Thus, the use of the pKM19 vector for maturation of an anti-CEA antibody significantly improves selection results.

Two antibody genes isolated from maturation library (clones 1 and 2), were cloned in pKM16, and soluble antibodies were produced and compared with the original soluble anti-CEA MA39 and the maturated E8 antibody obtained with canonical phagemid (Pavoni et al., 2006). FIG. 11 confirms the higher affinity of the maturated antibodies.

The specificity test on newly selected scFvs shows their low background reactivity with irrelevant proteins, comparable with that of the original antibody (FIG. 12).

Example 2

Construction of the Libraries Derived from TIL and Antibody Selection

Introduction

Identification of tumor-specific recombinant antibodies from display libraries derived from lymph nodes of cancer patients is described in [Clin. Exp. Immunol. 1997 109(1): 166-74; Int. J. Mol. Med. 2004 14(4):729-35; World J. Gastroenterol. 2004 10(18):2619-23].

It is known that about 7% of lymph node-derived, and between 18-68% of TIL-derived heavy chain antibody sequences belong to clonal groups (Cancer Immunol. Immunother. 2003 52(12):715-738). This indicates both tumor-draining lymph nodes and tumor-infiltrating lymphocytes are promising sources of tumor-specific antibodies. The authors showed, by PCR amplification of specific antibody gene regions deriving from ten primary breast tumors (none being of the rare MBC histological type) of patients aged between 49-79 years, that 7 of 10 of these samples (70%), have a prominence of IgG antibody expression, as compared with IgA subclass, which correlates with the oligoclonality of the hypervariable region of heavy chain antibodies, suggesting a specific immune response to tumor-expressed antigens. Clonality of tumor-derived antibodies was confirmed by sequencing analysis.

The authors identified a panel of tumor-specific antibodies from described libraries which were reactive with ED-B domain, MUC1, CEA and MCF7 breast carcinoma cells used in respective selections. It is interesting that in performing cell-based selection without subtractive panning step on normal breast epithelium, in contrast with numerous previously described selection protocols [Int J Mol Med. 2004 14(4): 729-35; World J Gastroenterol. 2004 10(18):2619-23; Int J Oncol. 2000 16(1):187-95; Cancer Res. 1999 59(11):2718-23; Biochem Biophys Res Cmmun. 2001 280(2):548-52], the authors isolated only one scFv out of 10 was not tumor-specific and recognized normal breast epithelium as well. This probably indicates that our modest-sized libraries contain a very restricted naturally occurring antibody repertoire provided by TIL-B, rather than a vast antibody repertoire created by antibody chain shuffling. Moreover, antibody selection from a mixture of PBL and TIL-derived libraries clearly shows the latter libraries to be more efficient in cell-based panning. In fact, all isolated anti-MCF7 single-chain antibodies appeared to be derived from tumor-infiltrating lymphocytes. In summary, TIL-derived libraries gave good results in all performed selections, providing a panel of human tumor-specific antibodies, which recognize tumor cell-surface antigens useful for therapy and diagnosis of cancer.

In this study we demonstrated that application of novel improved phage-display vector pKM19 led to the isolation of a large panel of antibodies derived from pieces of tumor tissue removed in tumor surgery, against known tumor antigens and entire tumor cells, and which are potentially useful in therapy of cancer. These results are similar to the results obtained by direct screening of soluble TIL-derived antibody expression libraries (Cancer Immunol. Immunother. 2002 51(2):79-90). The direct screening is an unbiased screening strategy which does not depend from phage amplification steps and results more efficient as compared to affinity selection performed with canonical display vectors, which failed to select tumor-specific antibodies in analogous works (Cancer Res. 2001 61(21):7889-99; Proc. Natl. Acad. Sci. U.S.A. 2001 98(22): 12659-64; Int. J. Cancer 2001 93:832-40). Our results indicate that pKM19 vector improves the selection results in comparison with classic display vectors and at the same time, provides possibility to apply affinity selection methodologies, facilitating manipulation with large libraries.

In conclusion, our results indicate that naturally occurring immune responses to tumor-related antigens exist in a majority of patients with breast cancer, not only in hystologically-defined MCB. Tumor samples as small as 0.2 g obtained as surgical material and, can be exploited as an appropriate source for generation of recombinant phage display libraries enriched for tumor-specific antibodies. Isolation of a panel of anti-tumor scFvs through selection against desirable protein targets, as well as against living breast carcinoma cells, shows this approach to be very promising for development of human therapeutic antibodies. Moreover, investigation of the protein targets eliciting production of tumor cell-specific antibodies in a tumor microenvironment may (i) provide important details about individual immunoreactivity of a given patient, affording a prognostic value; (ii) open a large perspective for discovery of novel tumor-specific antigens.

Methods

Tissue and Blood Samples

Specimens of breast carcinoma and fresh peripheral blood from breast cancer patients (B81-B96, EC23) were obtained from M. G. Vannini Hospital, Rome. All the human biological samples were obtained through informed consent.

Cell Lines

The breast carcinoma cell lines MCF-7 (ATCC Number: HTB-22), MDA-MB-468 (ATCC Number: HTB-132) and SkBr3 (ATCC Number: HTB-30), and colon adenocarcinoma cell line LoVo (ATCC Number: CCL-229) were maintained according to manufacturer's instructions. Human foreskin fibroblasts (HFF) were cultivated in DMEM supplemented with 10% FBS and 1% L-glutamine. Immortal breast epithelial cells MCF10-2A (ATCC number CRL-10781) [Cancer Res. 1990 50(18):6075-86] were propagated according to manufacturer's instructions, and used as negative controls in ELISA tests.

Purified Tumor Antigen Proteins

Human CEA protein, purified from colon carcinoma and liver metastases, was purchased from USBiological (#C1300-16, United States Biological, Swampscott, Mass.).

Biotinylated recombinant ED-B domain of fibronectin was obtained from Sigma-Tau S.p.A. (Pomezia, Rome).

Recombinant MUC1 protein was obtained in several steps. Two over-lapping oligonucleotides KM358 5′-ACT TCA GCT CCG GAC ACC CGT CCG GCT CCG GGT TCC ACC GCT CCG CCG GCT CAC GGT GTC-3′ [SEQ ID 97] and KM359 5′-CGG AGC CGG ACG GGT GTC CGG AGC TGA AGT GAC ACC GTG AGC CGG CGG AGC GGT GGA ACC-3′ [SEQ ID 98] encoded for 20-aa MUC1 repeat, were assembled in PCR-like process, in which 25 cycles of PCR amplification were performed with 0.2 μM/μL of KM358 and KM359. High-weight DNA band was then cut from agarose gel and ligated with a short adapter, obtained by annealing a KM328 5′-CT AGT TCG TCG GGT TCG TCG GGA-3′ [SEQ ID 99] oligonucleotide and a phospharylated one: KM329 5′-TCC CGA CGA ACC CGA CGA A-3′ [SEQ ID 100]. The resulting DNA fragment was purified from adapter excess, phosphorylated and cloned into digested and dephospharylated pGEX-SN [Int J Cancer. 2003 106(4):534-44], derived from pGEX-3X plasmid [Gene 1988 67:31-40] . GST-fused MUC1 recombinant protein, containing a 107-aa MUC1 sequence, containing 5.3 repeats, was purified according to standard methods [Gene 1988 67:31-40].

Purification of Lymphocytes from Peripheral Blood

The lymphocytes were isolated from 10 mL of fresh peripheral blood mixed with anticoagulant by using Ficoll-Paque Plus (Amersham Pharmacia Biotech, Sweden) according to manufacturer's instructions. mRNA was isolated from lymphocytes by using Dynabeads mRNA DIRECT Kit (Dynal, Norway).

RNA Extraction and cDNA Synthesis

Tumor specimens of about 200 mg from breast carcinoma patients were obtained as surgical discard samples and immediately frozen in liquid nitrogen. Total RNA was prepared by Total RNA Isolation System (Promega, Madison, Wis.) and purified to poly A⁺ RNA using PolyATract mRNA Isolation Systems (Promega). Five hundred ng of poly(A)⁺ RNA from breast carcinomas or 1 μg of the poly(A)⁺ RNA from the lymphocytes were used to synthesize full-length cDNAs by using SMART cDNA library construction kit (Clontech, Palo Alto, Calif.).

Analysis of Antibody Gene Expression by PCR

The hypervariable V(D)J antibody region was amplified by PCR from cDNA templates by using site-specific primers 5′-GGACACGGCT(G/C)TGTATTACTG-3′ [SEQ ID 101] and 5′-GCTGAGGAGACGGTGACC-3′ [SEQ ID 102] designed in designed in a study by Hansen and colleagues [Proc Natl Acad Sci USA 2001 98(22):12659-64]. IgG1, IgG2 and IgA subclass determination was done as described in [J Immunol. 2002 169(5):2701-11] by individually combining constant region-specific primers for IgG1, IgG2 and IgA genes (CG1d, CG2a and CA1, respectively) with a set of variable heavy chain primers: VH135, VH3a, VH3f, VH4, VH4b. These primers were designed for construction of human Fab libraries [Barbas C F III, Burton DR (1994) Monoclonal antibodies from combinatorial libraries. Cold Spring Harbor Laboratory Course Manual].

ScFv Library Construction

Antibody gene repertoire was amplified using set of primers designed for amplification of VH and VL antibody domains [Pope, A. R., Embleton, M. J. & Memaugh R. (1996) Construction and use of antibody gene repertoires. In: Antibody Engineering—A practical approach (McCafferty, J., Hoogenboom, H. & Chiswell D., eds), pp. 325, Oxford University Press] and scFv fragments were assembled in vitro as described earlier [Pope A Ret al., 1996]. The scFv fragments were then amplified by PCR with appropriate extension primers, incorporating NcoI, NotI restriction sites, permitting the cloning of the scFv genes into pKM19 vector. The resulting PCR products were purified on a 1% low-melting agarose gel (NuSieve 3:1 agarose, Rockland, Me.). The DNA fragments were digested with NcoI/NotI and inserted into pKM19 vector. The ligated DNA was used to transform competent bacterial cells DH5αF′ (supE44 ΔlacU169 (φ80 lacZΔM15) hsdR17 recA1 endA1gyrA96 thi-1 re1A1 F′ [traD36proAB⁺ lacI^qlacZΔM15]) by electroporation. The transformed cells were plated on 20 agar dishes (ø15 cm), containing LB agar, 100 μg/mL ampicillin and 1% glucose. After overnight incubation at 37° C., bacterial colonies were scraped from the plates and resuspended in LB, containing 10% of glycerol. Aliquots of this cell suspension were stored at −80° C. and used for phage amplification.

Phage Amplification

Forty μL of scraped bacterial cells were incubated in 40 mL of LB containing ampicillin and 1% glucose up to O.D.=0.2. The bacteria were collected by centrifuging and resuspended in 40 mL of LB with ampicillin without glucose. About 6×10⁹ pfu of helper M13K07 were added to each mL of cell suspension, incubated for 15 min at 37° C. without agitation and a further 2 h in a shaker. Kanamycin was added to final concentration 20 μg/mL and cells were incubated ON at 32° C. Phage was purified according to standard PEG/NaCl precipitation [Sambrook J, Fritsch E F, Maniatis T. Molecular cloning: A laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, 1989].

Cell-Based Selection of Antibodies from Phage-Displayed Library

MCF-7 semi-confluent cells (about 2×10⁷) were rinsed 3 times with PBS buffer and incubated with 2 mL of 2 mM EDTA in PBS for 15 min at 37° C. Ten mL of PBS containing 10 mM MgCl₂ were added to the cells, they were accurately removed by pipetting. The cells were collected by centrifuging, washed once with 10 mL of PBS/MgCl₂ and finally resuspended in 1 mL of freshly prepared blocking buffer: 4% non-fat dry milk, 0.05% Tween 20, 5×10¹¹ pfu of f1 UV-killed phage. The cells were blocked for 30 min at RT on rotating wheel, then collected and incubated for 1 h at 37° C. on the wheel with about 5×10¹¹ TU of freshly amplified scFv antibody library in 1 mL of blocking buffer. The cells were washed 5 times with PBS/Tween. The bound phage was eluted by adding 400 μL of 0.1 M HCl, pH 2.2 (adjusted by glycine). Cell suspension was incubated with elution solution for 10 min at RT, neutralized by 40 μL of 2M Tris-HCl, pH 9.6 and used for infection of bacterial cells. The bacteria were plated on two LB agar dishes (ø15 cm), containing 100 μg/mL ampicillin and 1% glucose. Scraped bacteria were used for phage amplification.

Affinity Selection on Purified Protein Targets.

CEA and MUC1 were biotinylated as described in [Harlow E. & Lane D. Antibody: A laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, 1988]. About 5×10¹¹ TU of freshly amplified scFv antibody libraries were preincubated with 50 μL of AD202 bacterial extract in blocking buffer for 30 min at 37° C. Twenty γ of a biotinylated protein were added to the reaction mixture and incubated for another h at 37° C. under gentle agitation. The bound phage was captured by using streptavidin-coated Dynabeads M-280 (112.05, Dynal, Oslo, Norway) according to manufacturer's instructions, washed 5-10 times with PBS/Tween, then, eluted and amplified as above.

ELISA Experiments

The cells were grown in 96-well plate until almost confluent. After discarding the growth medium, 100 μL of freshly prepared 4% paraformadehyde (#15710, Electron Microscopy Science, Hatfield, Pa.) in PBS were rapidly added for 10 min. The fixing solution was removed by pipetting and cells were incubated with blocking buffer (5% milk, 0.05% Tween 20 in PBS) for 30 min at RT. PEG purified phage in blocking buffer (1:1) was added to cells and incubated for 1 h at 37° C. under gentle agitation. The cells were washed 3 times and an anti-M13 HRP-conjugated antibody (Pharmacia) was used for developing the reaction. All assays were done in triplicate.

Immunofluorescence Staining

The cells were grown in a 24-well plate for cell culture (Nunc, Roskilde, Denmark), fixed as above and blocked with 3% BSA in PBS for 1 h at room temperature. PEG-purified phage in 1% BSA/PBS was added to the cells and incubated for 1 h under gentle agitation at 37° C. The cells were washed three times with 1% BSA/PBS and incubated with an anti-M13 mouse monoclonal antibody (27-9420-01, Amersham Biosciences) for 30 min at 37° C. The cells were washed as above and then incubated with an FITC-conjugated anti-mouse goat polyclonal antibody (554001, BD Biosciences Pharmingen, San Jose, Calif.) at a concentration of 5 μg/mL for 30.1 min at 37° C. under gentle agitation. After the last incubation, cells were washed five times, dried in the dark, mounted with Vectashield medium (Vector Laboratories, Inc. Burlingame, Calif.) and cover glasses, and analyzed using an inverted fluorescence microscope.

All antibodies are defined in table 5.

Results

Characterization of the Lymphoplasmatic Cell Infiltrate in Breast Tumor Samples

Ten tumor specimens from breast cancer patients (aged 47-79 years) for presence and nature of TIL-B by PCR amplification of V(D)J antibody segments (CDR3) and by comparison of representation of IgG and IgA antibody classes were examined.

The expression patterns of the antibody fragment genes was analyzed by semi-quantitative PCR from SMART cDNA template. The panel of cDNAs from ten breast carcinomas, from samples of normal breast, normal testis and peripheral blood lymphocytes from healthy donors were normalized by PCR amplification of a housekeeping gene, β-actin and are shown in FIG. 13A.

Hypervariable heavy chain antibody regions (V(D)J) were amplified as described in Materials and Methods. After analysis by agarose gel electrophoresis, the same PCR products were fractionated by high resolving 10% PAGE (FIG. 13B). In applying this technique, the authors observe that 7 out of 10 tumor-deriving samples contain various numbers of discrete bands, characterizing oligoclonality of the immune response in these patients, while the well-amplified normal breast and peripheral lymphocyte DNA fragments do not contain intensive bands and form a smear, consisting of the bands of different length. The observed oligoclonality of the immunoglobulins does not correlate with the age of the patients.

In order to analyze the antibody subclass distributions we amplified Ig genes from breast carcinoma cDNAs and normal breast, using subclass-specific primers. In agreement with previous assay, the 3 cDNA tumor samples, not containing oligoclonal bands in PCR-amplified V(D)J regions, have a prevalence of the IgA band in comparison with IgG1 and IgG2 bands, just as in a sample of normal breast where IgA generally represents the major Ig class (Br. Med. J. 1976 2(6034):503-506). On the other hand, samples showing oligoclonality in the first assay contain IgG1, or both IgG1 and IgG2 as dominant antibody bands, in contrast to normal breast. FIG. 14 shows four more characteristic examples along with normal breast sample.

Oligoclonality of TIL-B Derived Antibodies in Breast Cancer Patients was Confirmed by Sequencing

The authors chose two cDNA samples (B92, B93) giving strongest single bands in V(D)J test, for sequencing analysis. The nucleotide sequences of 17 and 13 randomly picked clones containing γ antibody genes deriving from B92 and B93 cDNA, respectively, were determined and their amino acid sequences were deduced. All 30 clones encoded in-frame correct organized heavy chains. More frequently isolated antibodies (B92-A and B93-A1) contained V(D)J regions of the exact length corresponding to the strong bands earlier observed in FIG. 13B (lines with B92 and B93 samples) (FIG. 15), thus indicating that both PCR amplification with variable heavy chain primers and the cloning step do not introduce any particular bias interfering with heavy chain frequencies in the constructed library.

As indicated FIG. 15, six somatic mutations were identified in antibody fragments. These mutations are localized in variable CDRs of γ chain of the same specificity, while only one mutation is found out of variable regions (P=0.0002). Therefore, oligoclonality of antibody repertoire derived from tumor tissue is a natural immune response occurring within tumor tissue driven by tumor antigens, and not an artifact introduced by PCR amplification.

Library Construction

Four scFv antibody libraries were constructed using seven cDNAs as template, characterized by oligoclonality of the immune response (see list of libraries in Table 2). Only library scFvEC23 (described in Example 1) was constructed from peripheral blood lymphocytes, obtained from a single patient with advanced stage of breast cancer.

TABLE 2
ScFv-antibody library list.
	Source of
Library	Ig genes	Patient (age)	Library complexity
ScFvB87	TIL	B87 (55)	4.7 × 105
ScFvB95	TIL	B95 (73)	1.1 × 107
ScFvB96	TIL	B96 (72)	2.6 × 107
ScFvmix	TIL	B85 (47), B91 (70),	2.4 × 107
		B92 (79), B93 (66)
ScFvEC23	PBL	EC23 (65)	1.8 × 107
mixTIL	TIL	—	ScFvB87 + ScFvB95 +
mixLIB	TIL + PBL		scFvB87 + scFvB95 +
			scFvmix + scFvEC23

Selection of Specific Anti-Tumor Antibodies from Phage Display Libraries Generated from TIL-B and PBL

The authors examined directly the possibility of selecting specific antibody fragments from phage libraries against common cancer antigens including ED-B domain of fibronectin [EMBO J. 1987 6(8):2337-42], MUC1 [Cancer Res. 1992 52(22):6365-70; Hum Pathol. 1995 26(4):432-9], and CEA [J. Clin. Lab. Anal. 5: 344-366; Semin Cancer Biol. 1999 9:67-81; Cancer Res. 2002 62:5049-5057]. Under conditions described in Materials and Methods a mixture of four TIL-derived scFv antibody-displayed libraries (scFvB87, scFvB95, scFvB96 and scFvmix) named mixTIL library (Table 2) and the scFvEC23 library were panned separately against three protein targets in several rounds. In every case we observed that pools of phage were already positive against the selecting antigen after second and third rounds of panning (FIG. 16). Randomly picked clones were tested for binding reactivity against the antigens. Results of the test of random phage clones from third round phage pools are summarized in Table 3. Positive clones were analyzed by fingerprinting using HaeIII and AluI double digestion and unique antibody clones were sequenced. FIG. 17 represents ELISA of single scFv-phages selected on purified antigens. The analyzed single clones strongly bind respective antigens and does not react with irrelevant proteins. This result indicates the pKM19 vector is a suitable tool for selection of anti-tumor antibodies from TIL and PBL-derived libraries.

TABLE 3
Result of selections through the use of three purified tumor antigens.
		Positive clones/	Isolated antibody
Target antigen	Library	tested clones	genes
ED-B	mixTIL	10/10	1
	scFvEC23	10/10	3
MUC1	mixTIL	2/16	1
	scFvEC23	6/8	2
CEA	mixTIL	17/20	4
	scFvEC23	15/20	3

Cell-Based Selection of Tumor-Specific Antibodies

The authors tested functionality of a single TIL-derived library (scFvB96) by selecting breast cancer-specific antibodies through cell-based panning on MCF-7 breast carcinoma cell line. Four libraries, including scFvB87, scFvB95, scFvmix and scFvEC23, were pooled together (library named mixLIB, table 2) and panned on the same type of cells. Four or five selection rounds on MCF-7 cells were necessary for mixLIB or scFvB96 libraries, respectively, in order to enrich the phage pools for specific cell binders (FIG. 18). Then, randomly picked clones were analyzed for entire scFv antibody presence. The full-length scFv-phage clones were tested by cell-based ELISA, and analyzed by fingerprinting, and various positive clones were sequenced. Amino acid sequences were deduced from DNA sequences, confirming correct, in-frame antibody structures. Clone analysis data are summarized in Table 4.

TABLE 4
Result of selection on intact/living human breast carcinoma MCF7 cells.
	MCF-7 selection
Library	scFvB96	mixLIB
Selection round	5	4
Full-length scFv/tested clones	12/40	30/40
Positive clones/full-length tested clones	5/12	22/30
Isolated antibody genes	2	8

The reactivity and specificity of cell-selected antibodies were verified by ELISA on both breast carcinoma cell lines: MCF-7, MDA-MB-468, and normal cells, as negative controls: MCF10-2A (human breast epithelium), HFF (human fibroblasts) (FIG. 19). Among 10 different selected scFv antibodies belonging to 7 specificity groups (mix7, mix12, mix25 antibodies have the same heavy chain sequence and different light chains; mix8 and mix39 antibodies have similar sequences with minor differences), 9 are specific for breast carcinoma cells, while only B96/4F scFv antibody binds normal epithelial cells as well.

Cell-Selected Antibodies Derive from TIL

Mix11, mix12, mix17, mix23 and mix39 scFv antibodies (Table 4) were selected from a mixture of PBL and TIL-derived libraries. The authors investigated the origin of these antibodies in order to see which type of library works better in equal selection conditions. One μL of each amplified library was used as template for PCR amplification with pair of oligonucleotide primers specific for each antibody (FIG. 20). This analysis shows that the 5 tested scFv antibodies, isolated from a mixture of libraries, belong to TIL-derived antibodies. Antibody genes of mix7 and mix25 antibodies (having the same heavy chain as mix12, table 5), and mix8 (similar to mix39, table 5) are believed to have a similar origin. For irrelevant anti-SP2 antibody, which was selected from the scFvEC23 library, its origin from PBL-derived library was confirmed. Anti-MUC1 MB5 and anti-CEA CB37 antibodies, which were selected from the mixture of four TIL-derived libraries (mixTIL) were shown to derive from the scFvmix and the scFvB96 libraries, respectively.

Fluorescent Staining of Tumor Cells

Binding specificities of several clones, including mix17, mix7 (FIG. 21), anti-Muc1 antibody MB5 and anti-CEA CB37 (FIG. 22) were assayed by immunofluorescent staining of tumor cells directly with scFvs antibodies displayed on the phage. Mix17 scFv recognizes major part of non-permealized MCF7 breast carcinoma cells in this experiment (FIG. 21A), while mix7 stains a low percentage of cells, probably apoptotic cells.

MB5 antibody intensively stains MCF7 cells, known for high MUC1 expression, and reacts well also with another breast carcinoma cell line, SkBr3(FIG. 22). CB37 antibody stains LoVo cells. No background staining for normal breast epithelium was observed for both MB5 and C1337 antibodies.

Example 3

Maturation of Anti-MUC1 and Anti-CEA scFv Antibodies

To increase affinity of tumor specific antibodies CB37 and MB5 we performed affinity maturation of the antibodies in vitro. The new maturation libraries were created by combination of genes of single VH chains derived from CB37 and MB5, respectively, with various genes of VL chains derived from TIL and PBL of tumor patients. The libraries were constructed as described in Example 1 and 2.

Methods

Affinity Selection

The affinity selection was performed by using biotinylated proteins as described in Example 2, with the difference that for first round of affinity selection we used 10 μg of the protein and for second only 50 ng. Clones found positive in ELISA were screened by PCR and fingerprinting with restriction enzymes AluI and HaeIII to identify different clones. The DNA sequence of the clones were determined. The antibody genes from clones having reactivity against target proteins higher than original antibodies were cloned in pKM16 to produce scFvs in soluble form as described in Example 1.

Characterization of Maturated Antibodies

The maturated antibody fragments were characterized for antigen binding.

The new anti-MUC1 antibodies MB5/C′1 and MB5/C′3 and anti-CEA maturated antibodies CB37/3B and CB37/9C (Table 5) in soluble form were characterized by Surface Plasmon Resonance (Biacore) as described in BMC Cancer 2006 6:41. Results are shown in table 6.

TABLE 5
Selected antibodies. MixTIL and MixLIB are
mixture of libraries defined in table 2.
		Library
Anti-	Anti-	used for
body	gen	selection	Nucleotide/Amino acid sequence
EDE1	ED-B	scFvEC23	CAGGTGCAGCTGCAGGAGTCTGGGGCTGAGGTGAAGAAG
			CCTGGGGCCTCAGTGAAGGTCTCCTGCAAGGCTTCTGGA
			TACACCTTCACCGGCTACTATATGCACTGGGTGCGACAG
			GCCCCTGGACAAGGGCTTGAGTGGATGGGATGGATCAAC
			CCTAACAGTGGTGGCACAAACTATGCACAGAAGTTTCAG
			GGCAGGGTCACCATGACCAGGGACACGTCCATCAGCACA
			GCCTACATGGAGCTGAGCAGGCTGAGATCTGACGACACG
			GCCGTGTATTACTGTGCGAGAGATTCGCCACAAAATTGT
			ACTAATGGTGTATGCCACCGGGGGAGTCATGTCCACTAC
			TACGGTATGGACGTCTGGGGCCAAGGCACCCTGGTCACC
			GTCTCTTCAGGTGGGGGCGGTTCAGGCGGAGGTGGCTCT
			GGCGGTGGCGGATCGCAGTCTGCCCTGACTCAGCCTGCC
			TCCGCGGCCGGGTCTCCTGGACAGTCAGTCACCATCTCC
			TGCACTGGAACCAGCAGTGATGTTGGTGGTTATAACTAT
			GTCTCCTGGTACCAACAGCACCCAGGCAAAGCCCCCAAA
			CTCATGATTTATGACGTCAATAAGCGGCCCTCAGGGGTC
			CCTGATCGCTTCTCTGCCTCCAAGTCTGGCAACACGGCC
			TCCCTGACCGTCTCTGGGCTCCAGGCTGACGATGAGGCT
			GATTACTACTGCGCTTCATATGCAGGCACCTACAGTTAT
			GTCTTCGGAACTGGGACCCAGCTCACCGTTTTAGGTGCG
			GCCGCAGGAGA [Seq ID 22]
			QVQLQESGAEVKKPGASVKVSCKASGYTFTGYYMHWVRQ
			APGQGLEWMGWINPNSGGTNYAQKFQGRVTMTRDTSIST
			AYMELSRLRSDDTAVYYCARDSPQNCTNGVCHRGSHVHY
			YGMDVWGQGTLVTVSSGGGGSGGGGSGGGGSQSALTQPA
			SAAGSPGQSVTISCTGTSSDVGGYNYVSWYQQHPGKAPK
			LMIYDVNKRPSGVPDRFSASKSGNTASLTVSGLQADDEA
			DYYCASYAGTYSYVFGTGTQLTVLGAAA [Seq ID 23]
EDE3	ED-B	scFvEC23	GAGGTGCAGCTGTTGCAGTCTGGGGCCGAGGTGAAGAAG
			CCTGGGGCCTCAGTGAAGGTCTCCTGCAAGGCTTCTGGA
			TACACCTTCACCGGCTACTATATGCACTGGGTGCGACAG
			GCCCCTGGACAAGGGCTTGAGTGGATGGGATGGATCAAC
			CCTAACAGTGGTGGCACAAACTATGCACAGAAGTTTCAG
			GGCAGGGTCACCATGACCAGGGACACGTCCATCAGCACA
			GCCTACATGGAGCTGAGCAGGCTGAGATCTGACGACACG
			GCCGTGTATTACTGTGCGAGAGATTCGCCACAAAATTGT
			ACTAATGGTGTATGCCACCGGGGGAGTCATGTCCACTAC
			TACGGTATGGACGTCTGGGGCCAGGGAACCCTGGTCACC
			GTCTCCTCAGGTGGGGGCGGTTCAGGCGGAGGTGGCTCT
			GGCGGTGGCGGATCGCAGTCTGCCCTGACTCAGCCTGCC
			TCCGCGGCCGGGTGTCTTGGACAGTCAGTCACCATCTCC
			TGCACTGGAACCAGCAGTGATGTTGGTGGTTATAAATAT
			GTCTCCTGGTACCAACAGCACCCAGGCAAAGCCCCCAAA
			CTCATGATTTATGACGTCAATAAGCGGCCCTCAGGGGTC
			CCTGATCGCTTCTTTGCCTCCAAGTCTGGCAACACGGCC
			TCCCTGACCGTCTCTGGGCTCCAGGCTGACGATGAGGCT
			GATTACTACTGCGCTTCATATGCAGGCACCTACAGTTAT
			GTCTTCGGAACTGGGACCCAGCTCACCGTTTTAGGTGCG
			GCCGCA [Seq ID 24]
			EVQLLQSGAEVKKPGASVKVSCKASGYTFTGYYMHWVRQ
			APGQGLEWMGWINPNSGGTNYAQKFQGRVTMTRDTSIST
			AYMELSRLRSDDTAVYYCARDSPQNCTNGVCHRGSHVHY
			YGMDVWGQGTLVTVSSGGGGSGGGGSGGGGSQSALTQPA
			SAAGCGLQSVTISCTGTSSDVGGYKYVSWYQQHPGKAPK
			LMIYDVNKRPSGVPDRFPASKSGNTASLTVSGLQADDEA
			DYYCASYAGTYSYVFGTGTQLTVLGAAA [Seq ID 25]
EDES	ED-B	scFvEC23	GAGGTGCAGCTGGTGGAGTCTGGGGCTGAGGTGAAGAAG
			CCTGGGGCCTCAGTGAAGGTCTCCTGCAAGGCTTCTGGA
			TACACCTTCACCGGCTACTATATGCACTGGGTGCGACAG
			GCCCCTGGACAAGGGCTTGAGTGGATGGGATGGATCAAC
			CCTAACAGTGGTGGCACAAACTATGCACAGAAGTTTCAG
			GGCAGGGTCACCATGACCAGGGACACGTCCATCAGCACA
			GCCTACATGGAGCTGAGCAGGCTGAGATCTGACGACACG
			GCCGTGTATTACTGTGTGAGAGGTTCGCCACAAAATTGT
			ACTAATGGTGTATGCCACCGGGGGAGTCATGTCCACTAC
			TACGGTATGGACGTCTGGGGCCAAGGGACCACGGTCACC
			GTCTCCTCAGGTGGGGGCGGTTCAGGCGGAGGTGGCTCT
			GGCGGTGGCGGATCGCAGTCTGCCCTGACTCAGCCTGCC
			TCCGTGTCTGGGTCTCCTGGACAGTCGATCACCATCTCC
			TGCACTGGAACCAGCAGTGATGTTGGGAGTTATAACCTT
			GTCTCCTGGTACCAACAGCACCCAGGCAAAGCCCCCAAA
			CTCATGATTTATGAGGTCAGTAATCGGCCCTCAGGGGTT
			TGTAATCGCTTCTCTGGCTCCAAGTCTGGCAACACGGCC
			TCCCTGACCATCTCTGGGCTCCAGGCTGAGGACGAGGCT
			GATTATTACTGCAGCTCATATACAAGCAGCAGCACTCTC
			GAGGTGTTCGGCGGAGGGACCCAGCTCACCGTTTTAGGT
			GCGGCCGCA [Seq ID 26]
			EVQLVESGAEVKKPGASVKVSCKASGYTFTGYYMHWVRQ
			APGQGLEWMGWINPNSGGTNYAQKFQGRVTMTRDTSIST
			AYMELSRLRSDDTAVYYCVRGSPQNCTNGVCHRGSHVHY
			YGMDVWGQGTTVTVSSGGGGSGGGGSGGGGSQSALTQPA
			SVSGSPGQSITISCTGTSSDVGSYNLVSWYQQHPGKAPK
			LMIYEVSNRPSGVCNRFSGSKSGNTASLTISGLQAEDEA
			DYYCSSYTSSSTLEVFGGGTQLTVLGAAA [Seq ID 27]
EDBS	ED-B	mixTIL	CAGGAGGTGCAGCTGGTGGAGTCTGGGGGTGGCTTGGTC
			CAGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCCTCT
			GGATTCACCCTCAGTAGCTATGCTATGCACTGGGTCCGC
			CAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAACTATT
			AGTGGTGGTGGTGGTAGCACATACTACGCAGACTCCGTG
			AAGGGCCGGTTCACCATCTCCAGAGACAATTCCAAGAAC
			ACGCTGTATCTGCAAATGAACAGCCTGAGAGCCGAGGAC
			ACGGCCGTATATTACTGTGCGAGACGGGGGCGGGCTTTT
			GATATCTGGGGCCAAGGGACCACGGTCACCGTCTCCTTA
			GGTGGAGGCGGTTCAGGCGGAGGTGGCTCTGGCGGTGGC
			GGATCGCAGTCTGTGTTGACGCAGCCGCCCTCAGTGTCT
			GGGGCCCCAGGGCAGAGGGTCACCATCTCCTGCACTGGG
			AGCAGCTCCAACATCGGGGCGGGGTATGATGTACACTGG
			TACCAGCAGCTTCCAGGAACAGCCCCCAAACTCCTCATT
			TATGGTAACAGCAATCGGCCCTCAGGGGTCCCTGACCGA
			TTCTCTGGCTCCAAGTCTGGCACCTCAGCCTCCCTGGCC
			ATCACTGGGCTCCAGGCTGAGGATGAGGCTGATTATTAT
			TGCTCCAGTCCTATGATCAGCAGCCTGAGTGGTCATGTG
			GTATTCGGCGGAGGGACCAAGGTGACCGTCCTAGGTGCG
			GCCGCA [Seq ID 28]
			QEVQLVESGGGLVQPGGSLRLSCAASGFTLSSYAMHWVR
			QAPGKQLEWVSTISGGGGSTYYADSVKGRFTISRDNSKN
			TLYLQMNSLRAEDTAVYYCARRGRAFDIWGQGTTVTVSL
			GGGGSGGGGSGGGGSQSVLTQPPSVSGAPGQRVTISCTG
			SSSNIGAGYDVHWYQQLPGTAPKLLIYGNSNRPSGVPDR
			FSGSKSGTSASLAITGLQAEDEADYYCSSPMISSLSGHV
			VFGGGTKVTVLGAAA [Seq ID 29]
ME1	MUC1	scFvEC23	CAGGTGCAGCTGGTGCAGTCTGGGGCTGAGGTGAAGAAG
			CCTGGGGCCTCAGTGAAGGTCTCCTGCAAGGCTTCTGGA
			TACACCTTCACCGGCTACTATATGCACTGGGTGCGACAG
			GCCCCTGGACAAGGGCTTGAGTGGATGGGATGGATCAAC
			CCTAACAGTGGTGGCACAAACTATGCACAGAAGTTCCAG
			GGCAGGGTCACCATGACCAGGGACACGTCCATTGGCACA
			GTCTACATGGAGTTGAGCAGCCTGACATCTGACGACACG
			GCCATGTATTATTGTGCGAGAAACAATGTTGCTATGGGT
			TATACTATGGACGTCTGGGGCCAAGGGACAATGGTCACC
			GTCTCTTCAGGTGGAGGCGGTTCAGGCGGAGGTGGCTCT
			GGCGGTGGCGGATCGCAGTCTGCCCTGACTCAGCCTGCC
			TCCGCGTCCGGGTCTCCTGGACAGTCAGTCACCATCTCC
			TGCACTGGAACCAGCAGTGACGTTGGTGGTTATAACTAT
			GTCTCCTGGTACCAACAGCACCCAGGCAAAACCCCCAAA
			CTCTTGATTTATGAGGTCAGTAGTCGGCCCTCAGGGGTT
			TCTAATCGCTTCTCTGGCTCCAAGCCTGGCAACACGGCC
			TCCCTGACCATCTCTGGTCTCCAGGCTGAGGACGAGGCT
			GATTATTACTGCATCTCATATACAAGCAGCAACACTTGG
			GTGTTCGGCGGAGGGACCCAGCTCACCGTTTTAGGTGCG
			GCCGCA [Seq ID 30]
			QVQLVQSGAEVKKPGASVKVSCKASGYTFTGYYMHWVRQ
			APGQGLEWMGWINPNSGGTNYAQKFQGRVTMTRDTSIGT
			VYMELSSLTSDDTAMYYCARNNVAMGYTMDVWGQGTMVT
			VSSGGGGSGGGGSGGGGSQSALTQPASASGSPGQSVTIS
			CTGTSSDVGGYNYVSWYQQHPGKTPKLLIYEVSSRPSGV
			SNRFSGSKPGNTASLTISGLQAEDEADYYCISYTSSNTW
			VFGGGTQLTVLGAAA [Seq ID 31]
ME2	MUC1	scFvEC23	GAGGTGCAGCTGTTGCAGTCTGGGGCGGAGGTGAAGAAG
			CCTGGGGCCTCAGTGAAGGTCTCCTGCAAGGCTTCTGGA
			TACACCTTCACCGGCTACTATATGCACTGGGTGCGACAG
			GCCCCTGGACAAGGGCTTGAGTGGATGGGATGGATCAAC
			CCTAACAGTGGTGGCACAAACTATGCACAGAAGTTTCAG
			GGCAGAGTCACCATGACCAGGAACACCTCCATAAGCACA
			GCCTACATGGAGCTGAGCAGCCTGAGATCTGAGGACACG
			GCCGTGTATTACTGTGCGGGTCAGGAGGCACATGGGGAC
			GGTATGGACGTCTGGGGCCAAGGGACCACGGTCACCGTC
			TCCTCGGTGGAGCGAGGTGGCTCTGGCGGTGGCGGATCG
			CAGTCTGCCCTGACTCAGCCTGCCTCCGCGTCCGGGTCT
			CCTGGACAGTCGATCACCATCTCCTGCACTGGAACCAGC
			GGTGACGTTGGTGGTTATAACTATGTCTCCTGGTACCAA
			CAGCACCCAGGCAAAGCCCCCAAACTCATGATTTATGAA
			GTCAGTAATCGGCCCTCAGGGGTTTCTAATCGCTTCTCT
			GGCTCCAAGTCTGGCAGCACGGCCTCCCTGACCATCTCT
			GGGCTCCAGGCTGAGGACGAGGCTGATTATTACTGCGTC
			TCATATACAAGCAGAAACACTTATGTCTTCGGATCCGGG
			ACCCAGCTCACCGTTTTAGGTGCGGCCGCGA [Seq ID
			32]
			EVQLLQSGAEVKKPGASVKVSCKASGYTFTGYYMHWVRQ
			APGQGLEWMGWINPNSGGTNYAQKFQGRVTMTRNTSIST
			AYMELSSLRSEDTAVYYCAGQEAHGDGMDVWGQGTTVTV
			SSVERGGSGGGGSQSALTQPASASGSPGQSITISCTGTS
			GDVGGYNYVSWYQQHPGKAPKLMIYEVSNRPSGVSNRFS
			GSKSGSTASLTISGLQAEDEADYYCVSYTSRNTYVFGSG
			TQLTVLGAAA [Seq ID 33]
MB5	MUC1	mixTIL	GAGGTGCAGCTGGTGGAGTCTGGAGCTGAGGTGAAGAAG
			CCCGGGGCCTCAGTGAAGGTCTCCTGCAAGGCTTCTGGA
			TACACCTTCACCGCCTCCTATATGCACTGGGTGCGACAG
			GCCCCTGGACAAGGGCTTGAGTGGATGGGATGGTTCAAC
			CCTAATAGTGGTGGCACAAACTATGCACAGAAGTTTCAG
			GGCAGGGTCACCATGACCGGGGACACGTCCACCAGCACA
			GGCTATATGGAGCTGAGCAGGCTGACATCTGACGACGCG
			NCCGTGTATTATTGTGCGAGAGATCGGGCCTCTGCTATG
			GGCGTCTGGGGCCAAGGCACCCTGGTCACCGTCTCCTCA
			GGTGGAGGCGGTTCAGGCGGAGGTGGCTCTGGCGGNGGC
			CGATCGCAGTCTGCCCTGACTCAGCCTGCCTCCGCGTCC
			GGGTCTCCTGGACAGTCAGTCACCATCTCCTGCACTGGA
			ACCAGCAGTGACGTTGGTGGTTATAACTATGTCTCCTGG
			TACCAACAGCACCCAGGCAAAGCCCCCAAACTCATGATT
			TATGACGTCAATAAGCGGCCCTCAGGGGTCCCTGATCGC
			TTCTCTGGCTCCAAGTCTGGCAACACGGCCTCCCTGACC
			GTCTCTGGGCTCCAGGCTGAGGATGAGGCTGATTATTAC
			TGCAGCTCATATGCAGGTAGTAACACTTTCCTATTCGGC
			GGAGGGACCCAGCTCACCGTTTTAGGTGCGGCCGCA
			[Seq ID 2]
			EVQLVESGAEVKKPGASVKVSCKASGYTFTASYMHWVRQ
			APGQGLEWMGWFNPNSGGTNYAQKFQGRVTMTGDTSTST
			GYMELSRLTSDDATVYYCARDRASAMGVWGQGTLVTVSS
			GGGGSGGGGSGGGGSQSALTQPASASGSPGQSVTISCTG
			TSSDVGGYNYVSWYQQHPGKAPKLMIYDVNKRPSGVPDR
			FSGSKSGNTASLTVSGLQAEDEADYYCSSYAGSNTFLFG
			GGTQLTVLGAAA [Seq ID 3]
MB5/	MUC1	maturation	ATGGAGGAGGTGCAGCTGCAGGAGTCTGGAGCTGAGGTG
C′1		library	AAGAAGCCCGGGGCCTCAGTGAAGGTCTCCTGCAAGGCT
		based on	TCTGGATACACCTTCACCGCCTCCTATATGCACTGGGTG
		MB5 clone,	CGACAGGCCCCTGGACAAGGGCTTGAGTGGATGGGATGG
		as	TTCAACCCTAATAGTGGTGGCACAAACTATGCACAGAAG
		described	TTTCAGGGCAGGGTCACCATGACCGGGGACACGTCCACC
		in Example	AGCACAGGCTATATGGAGCTGAGCAGGCTGACATCTGAC
		3	GACGCGGCCGTGTATTATTGTGCGAGAGATCGGGCCTCT
			GCTATGGGCGTCTGGGGCCAAGGAACCCTGGTCACCGTC
			TCCTCAGGTGGAGGCGGTTCAGGCGGAGGTGGCTCTGGC
			GGTGGCGGATCCCAGTCTGCCCTGACTCAGCCTGCCTCC
			GTGTCTGGGTCTCCTGGACAGTCGATCACCATCTCCTGC
			ACTGGAACCAGCAGTGACGTTGGTGGTTATAACTATGTC
			TCCTGGTACCAACAGCACCCAGGCAAAGCCCCCAAACTC
			ATGATTTATGATGTCAGTCATCGGCCCTCAGGGATTTCT
			AATCGCTTCTCTGGCTCCAAGTCTGGCAACACGGCCTCC
			CTGACCATCTCTAGGCTCCAGGCTGAGGACGAGGCTGAT
			TATTACTGCAGCTCATATACAAGCAGTAACACTTTCATC
			TTCGGAACTGGGACCCAGCTCACCGTTTTAGGTGCGGCC
			GC [Seq ID 4]
			MEEVQLQESGAEVKKPGASVKVSCKASGYTFTASYMHWV
			RQAPGQGLEWMGWFNPNSGGTNYAQKFQGRVTMTGDTST
			STGYMELSRLTSDDAAVYYCARDRASAMGVWGQGTLVTV
			SSGGGGSGGGGSGGGGSQSALTQPASVSGSPGQSITISC
			TGTSSDVGGYNYVSWYQQHPGKAPKLMIYDVSHRPSGIS
			NRFSGSKSGNTASLTISRLQAEDEADYYCSSYTSSNTFI
			FGTGTQLTVLGAA [Seq ID 5]
MB5/	MUC1	maturation	ATGGAGCAGGTGCAGCTGGTGCAGTCTGGAGCTGAGGTG
C′3		library	AAGAAGCCCGGGGCCTCAGTGAAGGTCTCCTGCAAGGCC
		based on	TCTGGATACACCTTCACCGCCTCCTATATGCACTGGGTG
		MB5 clone,	CGACAGGCCCCTGGACAAGGGCTTGAGTGGATGGGATGG
		as	TTCAACCCTAATAGTGGTGGCACAAACTATGCACAGAAG
		described	TTTCAGGGCAGGGTCACCATGACCGGGGACACGTCCACC
		in Example	AGCACAGGCTATATGGAGCTGAGCAGGCTGACATCTGAC
		3	GACGCGGCCGTGTATTATTGTGCGAGAGATCGGGCCTCT
			GCTATGGGCGTCTGGGGCCAAGGCACCCTGGTCACCGTC
			TCCTCAGGTGGAGGCGGTTCAGGCGGAGGCGGCTCTGGC
			CGTGGCGGATCGCAGTCTGCCCTGACTCAGCCTGCCTCC
			GTGTCTGGGTCTCCTGGACAGTCGATCACCATCTCCTGC
			ACTGGAACCAGCAGTGACGTTGGTGGTTATAACTATGTC
			TCCTGGTACCAACAGCACCCAGGCAAAGCCCCCAAACTC
			ATGATTTATGATGTCACTAATCGGCCTTCAGGGGTTTCT
			AGTCGCTTCTCTGGCTCCAAGTCTGGCAACACGGCCTCC
			CTGACCATCTCTGGACTCCAGACTGAGGACGAGGCTGAT
			TATTACTGCAACTCATTTACAAGCAGCAACACTTATGTC
			TTCGGAACTGGGACCCAGCTCACCGTTTTAGGTGCGGCC
			GC [Seq ID 6]
			MEQVQLVQSGAEVKKPGASVKVSCKASGYTFTASYMHWV
			RQAPGQGLEWMGWFNPNSGGTNYAQKFQGRVTMTGDTST
			STGYMELSRLTSDDAAVYYCARDRASAMGVWGQGTLVTV
			SSGGGGSGGGGSGGGGSQSALTQPASVSGSPGQSITISC
			TGTSSDVGGYNYVSWYQQHPGKAPKLMIYDVTNRPSGVS
			SRFSGSKSGNTASLTISGLQTEDEADYYCNSFTSSNTYV
			FGTGTQLTVLGAA [Seq ID 7]
CB3	CEA	mixTIL	GAGGTGCAGCTGTTGCAGTCTGGGGCTGAGGTGAAGAAG
			CCTGGGGCCTCAGTGAAGGTCTCCTGCAAGGCTTCTGGA
			TACACCTTCACCGGCTCCTATATTCACTGGGTGCGACAG
			GCCCCTGGACAAGGGCTTGAGTGGATGGGACGGATGAAC
			CCTAACAGTGGTGACACAAACTATGCACAGAAGTTTCAG
			GGCCGGGTCACCATGACCAGGGACACGTCCATCAGCACA
			GCCTACATGGAGCTGAGCAGGCTGAGATCTGACGACACG
			GCCGTGTACTACTGTGCGACGGAGGGAGTGGCTTTACGT
			CCCGGTGCTTTTGATTTCTGGGGCCAAGGGACCCAGCTC
			ACCGTTTTAGGTGCGGCCGCA [Seq ID 34]
			EVQLLQSGAEVKKPGASVKVSCKASGYTFTGSYIHWVRQ
			APGQGLEWMGRMNPNSGDTNYAQKFQGRVTMTRDTSIST
			AYMELSRLRSDDTAVYYCATEGVALRPGAFDFWGQGTQL
			TVLGAAA [Seq ID 35]
CB37	CEA	mixTIL	GAGGAGGTGCAGCTGGTGCAGTCTGGAGGAGGCTTGATC
			CAGCCGGGGGGGTCCCTGAGACTCTCTTGTGTAGCCTCT
			GAGTTCAACGTCAGAAGCAACTACATGAGCTGGGTCCGC
			CAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAGTTATG
			TATGACGGCGGTAGTACATACTACGCAGACTCCGTGAAG
			GGCCGATTCACCATCTCCAGAGACAATTCTAAGAACACG
			GTGTATCTTCAAATGAACAGCCTGAGAGCCGAGGACACG
			GCCGTCTATTACTGTGCGAGAGGCGGATTGGGGTTGCCT
			ACAATCGCGTCTTGGGAGATCTGGGGCCAAGGGACAATG
			GTCACCGTCTCTTCAGGTGGAGGCGGTTCTGGCGGAGGT
			GGCTCTGGCGGTGGCGGATCGTCCTATGTGCTGACTCAG
			CCACCCTCGGTGTCAGTGGCCCCAGGAAAGACGGCCACG
			ATTACCTGTGCGGGAAACAATATAGGAAGTAACAGTGTA
			TACTGGTACCAGCAGAAACCAGGCCTGGCCCCTGTACTG
			GTCGTCTATGATGATAGAGACCGGCCCTCAGGGATCCCT
			GAGCGATTCTCTGGCTCCAAATCCGGGAACACGGCCACC
			CTGACCATCAGCAGGGTCGAGGCCGGGGATCAGGCCGAC
			TATTCTTGTCAGGTGTGGGATCCTAGTAGTGATCACCTC
			TATGTCTTCGGAACTGGGACCCAGCTCACCGTTTTAGGT
			GCGGCCGCA [Seq ID 8]
			EEVQLVQSGGGLIQPGGSLRLSCVASEFNVRSNYMSWVR
			QAPGKGLEWVSVMYDGGSTYYADSVKGRFTISRDNSKNT
			VYLQMNSLRAEDTAVYYCARGGLGLPTIASWEIWGQGTM
			VTVSSGGGGSGGGGSGGGGSSYVLTQPPSVSVAPGKTAT
			ITCAGNNIGSNSVYWYQQKPGLAPVLVVYDDRDRPSGIP
			ERFSGSKSGNTATLTISRVEAGDEADYSCQVWDPSSDHL
			YVFGTGTQLTVLGAAA [Seq ID 9]
CB40	CEA	mixTIL	=CB37
CB41	CEA	mixTIL	GAGGAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTGGTC
			CAGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCCTCT
			GGATTCACCGTCAGTAGCAACTACATGAGCTGGGTCCGC
			CAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAGTTGTT
			TATAGCGGTGGTAGCACATACTACGCAGACTCCGTGAAG
			GGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACG
			CTGTATCTTCAAATGAACAGCCTGAGAGCTGAGGACACG
			GCTGTGTATTACTGTGCGACAGACCTAGGGGGGACTACA
			GTTTGGCGCTACTACGGTATGGACGTCTGGGGCCAAGGG
			ACCACGGTCACCGTCTCCTCAGGTGGAGGCGGTTCAGGC
			GGAGGTGGCTCTGGCGGTGGCGGATCGTCCTATGTGCTG
			ACTCAGCCACCCTCGGTGTCAGTGGCCCCAGGAAAGACG
			GCCACGATTACCTGTGCGGGAAACAATATAGGAAGTAAC
			AGTGTATACTGGTACCAGCAGAAACCAGGCCTGGCCCCT
			GTACTGGTCGTCTATGATGATAGAGACCGGCCCTCAGGG
			ATCCCTGGGCGATTCTCTGGCTCCAAATCCGGGAACACG
			GCCACCCTGACCATCAGCAGGGTCGAGGCCGGGGATGAG
			GCCGACTATTCTTGTCAGGTGTGGGATCCTAGTAGTGAT
			CACCTCTATGTCTTCGGAACTGGGACCCAGCTCACCGTT
			TTAGGTGCGGCCGCA [Seq ID 36]
			EEVQLVESGGGLVQPGGSLRLSCAASGFTVSSNYMSWVR
			QAPGKGLEWVSVVYSGGSTYYADSVKGRFTISRDNSKNT
			LYLQMNSLRAEDTAVYYCARDLGGTTVWRYYGMDVWGQG
			TTVTVSSGGGGSGGGGSGGGGSSYVLTQPPSVSVAPGKT
			ATITCAGNNIGSNSVYWYQQKPGLAPVLVVYDDRDRPSG
			IPGRFSGSKSGNTATLTISRVEAGDEADYSCQVWDPSSD
			HLYVFGTGTQLTVLGAAA [Seq ID 37]
CB53	CEA	mixTIL	GAGGAGGTGCAGCTGGTGGAGTCTGGAGGAGACTTGATC
			CAGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCCTCT
			GGGTTTACCGTCGGTAGCAACTACATGAGCTGGGTCCGC
			CAGGCTCCAGGGAAGGGGCTGGAATGGGTCTCAGTTATT
			TATAGCGGTGGTAGTACATACTACGCAGACTCCGTGAAG
			GGCCGATTCACCATCTCCAGAGACAATTCCAAGAACACG
			CTGTATCTTCAAATGAACAGCCTGAGAGCCGAGGACACG
			GCCGTGTATTACTGTGTGAGAGATAGGGGTGATGCTTTT
			GATATCTGGGGCCAAGGGACAATGGTCACCGTCTCTTCA
			GGTGGAGGCGTTCCAGGCGGAGGTGGCTCTGGCGGTGGC
			GGATCGTCCTATGCGCTGACTCAGCCACCCTCGGTGTCA
			GTGGCCCCAGGAAAGACGGCCACGATTACCTGTGCGGGA
			AACAATATAGGAAGTAACAGTGTATACTGGTACCAGCAG
			AAACCAGGCCTGGCCCCTGTACTGGTCGTCTATGATGAT
			AGCGACCGGCCCTCAGGGATGTCTGAGCGATTCTCTGGC
			TCCAAATCCGGGAACACGGCCACCCTGACCATCAGCAGG
			GTCGAGGCCGGGGATGAGGCCGACTATTCTTGTCAGGTG
			TGGGATCCTAGTAGTGATCACCTCTATGTCTTCGGAACT
			GGGACCCAGCTCACCGTTTTAGGTGCGGCCGCA [Seq
			ID 38]
			EEVQLVESGGDLIQPGGSLRLSCAASGFTVGSNYMSWVR
			QAPGKGLEWVSVIYSGGSTYYADSVKGRFTISRDNSKNT
			LYLQMNSLRAEDTAVYYCVRDRGDAFDIWGQGTMVTVSS
			GGGVPGGGGSGGGGSSYALTQPPSVSVAPGKTATITCAG
			NNIGSNSVYWYQQKPGLAPVLVVYDDSDRPSGMSERFSG
			SKSGNTATLTISRVEAGDEADYSCQVWDPSSDHLYVFGT
			GTQLTVLGAAA [Seq ID 39]
CB60	CEA	mixTIL	=CB41
CB37/	CEA	maturation	ATGGAGGAGGTGCAGCTGGTGCAGTCTGGAGGAGGCTTG
3B		library	ATCCAGCCGGGGGGGTCCCTGAGACTCTCTTGTGTAGCC
		based on	TCTGAGTTCAACGTCAGAAGCAACTACATGAGCTGGGTC
		CB37	CGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAGTT
		clone, as	ATGTATGACGGCGGTAGTACATACTACGCAGACTCCGTG
		described	AAGGGGCGATTCACCATCTCCAGAGACAATTCTAAGAAC
		in Example	ACGGTGTATCTTCAAATGAACAGCCTGAGAGCCGAGGAC
		3.	ACGGCCGTCTATTACTGTGCGAGAGGCGGATTGGGGTTG
			CCTACAATCGCGCCTTGGGAGATCTGGGGCCAAGGGACA
			ATGGTCACCGTCTCTTCAGGTGGAGGCGGTTCAGGCGGA
			GGTGGCTCTGGCGGTGGCGGATCGTCCTATGTGCTGACT
			CAGCCACCCTCGGTGTCAGTGGCCCCAGGAAAGACGGCC
			ACGATTACCTGTGCGGGAAACAATATAGGAAGTAACAGT
			GTATACTGGTACCAACAAAAACCAGGCCTGGCCCCTGTA
			CTGGTCGTCTATGATGATAGAGACCGGCCCTCAGGGATC
			CATGAGCGATTCTCTGGCTCCAAATCCGGGAACACGGCC
			ACCCTGACCATCAGCAGGGTCGAGGCCGGGGATGAGGCC
			GACTATTCTTGTCAGGTGTGGGATCCTAGTAGTGATCAC
			CTCTATGTCTTCGGAACTGGGACCCAGCTCACCGTTTTA
			GGTGCGGCCGC [Seq ID 10]
			MEEVQLVQSGGGLIQPGGSLRLSCVASEFNVRSNYMSWV
			RQAPGKGLEWVSVMYDGGSTYYADSVKGRFTISRDNSKN
			TVYLQMNSLRAEDTAVYYCARGGLGLPTIAPWEIWGQGT
			MVTVSSGGGGSGGGGSGGGGSSYVLTQPPSVSVAPGKTA
			TITCAGNNIGSNSVYWYQQKPGLAPVLVVYDDRDRPSGI
			HERFSGSKSGNTATLTISRVEAGDEADYSCQVWDPSSDH
			LYVFGTGTQLTVLGAA [Seq ID 11]
CB37/	CEA	maturation	ATGGAGGAGGTGCAGCTGGTGCAGTCTGGAGGAGGCTTG
9C		library	ATCCAGCCGGGGGGGTCCCTGAGACTCTCTTGTGTAGCC
		basedon	TCTGAGTTCAACGTCAGAAGCAACTACATGAGCTGGGTC
		CB37	CGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAGTT
		clone,as	ATGTATGACGGCGGTAGTACATACTACGCAGACTCCGTG
		described	AAGGGCCGATTCACCATCTCCAGAGACAATTCTAAGAAC
		inExample	ACGGTGTATCTTCAAATGAACAGCCTGAGAGCCGAGGAC
		3.	ACGGCCGTCTATTACTGTGCGAGAGGCGGATTGGGGTTG
			CCTACAATCGCGTCTTGGGAGATCTGGGGCCAAGGGACA
			ATGGTCACCGTCTCTTCAGGTGGAGGCGGTTCAGGCGGA
			GGTGGCTCTGGCGGTGGCGGATCGTCCTATGTGCTGACT
			CAGCCACCCTCGGTGTCAGTGGCCCCAGGAAAGACGGCC
			ACGATTACCTGTGCGGGAAACAATATAGGAAGTAACAGT
			GTATACTGGTACCAGCAGAAACCAGGCCTGGCCCCTGTA
			CTGGTCGTCTATGATGATAGAGACCGGCCCTCAGGGCTC
			CCCGGGCGATTCTCTGGCTCCAAATCCGGGAACACGGCC
			ACCCTGACCATCAGCAGGGTCGAGGCCGGGGATGAGGCC
			GACTATTCTTGTCAGGTGTGGGATCCTAGTAGTGATCAC
			CTCTATGTCTTCGGAACTGGGACCCAGCTCACCGTTTTA
			GGTGCGGCCGC [Seq ID 12]
			MEEVQLVQSGGGLIQPGGSLRLSCVASEFNVRSNYMSWV
			RQAPGKGLEWVSVMYDGGSTYYADSVKGRFTISRDNSEN
			TVYLQMNSLRAEDTAVYYCARGGLGLPTIASWEIWGQGT
			MVTVSSGGGGSGGGGSGGGGSSYVLTQPPSVSVAPGKTA
			TITCAGNNIGSNSVYWYQQKPGLAPVLVVYDDRDRPSGL
			PGRFSGSKSGNTATLTISRVEAGDEADYSCQVWDPSSDH
			LYVFGTGTQLTVLGAA [Seq ID 13]
anti-	SP2	scFvEC23	ATGGAGGAGGTGCAGCTGGTGGAGTCTGGGGGAGCCTTG
SP2			GTACAGCCTGGGGGGTCCCTGAGAATCTCTTGTGTAGGC
			TCTGGATTCACCTTCCGACAGCATGACATGAGCTGGGTC
			CGCCAGGCTCCTGGGAAGGGGCTGGAGTGGGTCGCAACT
			ATAAGTGGAAGTGCTGATAACACATTTTACGCAGACTCC
			GTGAAGGGCCGGTTCACCATCTCCAGAGACAATTCCAAG
			AACACGCTGTATCTGCAGATGAACACCCTGAAAGCCGAC
			GACACGGCCGTATATTACTGTGCGAAGAAATATATAGAA
			CCAGGTGCTACCCGATTTGACTACTGGGGCCAGAGAACC
			CTGGTCACCGTCTCCTCAGGTGGAGGCGGTTCAGGCGGA
			GGTGGCTCTGGCGGTGGCGGATCGGATGTTGTGATGACT
			CAGTCTCCACTCTCTCTGTCCGTCACCCCTGGACAGCCG
			GCCTCCATCTCCTGCAAGTCTAGTCAGAGCCTCCTGCAT
			AGTGATGGAAAGACCTATTTGTATTGGTACCTGCAGAAG
			CCAGGCCAGTCTCCACAGCTCCTGATCTATGAAGTTTCC
			AACCGGTTCTCTGGAGTGCCAGATAGGTTCAGTGGCAGC
			GGGTCAGGGACAGATTTCACACTGAAAATCAGCCGGGTG
			GAGGCTGAGGATGTTGGGGTTTATTACTGCATGCAAAGT
			ATACAGCTCCCGATCACCTTCGGCCAAGGGACACGACTG
			GAGATTAAACGTGCGGCCGC [Seq ID 40]
			MEEVQLVESGGALVQPGGSLRISCVGSGFTFRQHDMSWV
			RQAPGKGLEWVATISGSADNTFYADSVKGRFTISRDNSK
			NTLYLQMNTLKADDTAVYYCAKKYIEPGATRFDYWGQRT
			LVTVSSGGGGSGGGGSGGGGSDVVMTQSPLSLSVTPGQP
			ASISCKSSQSLLHSDGKTYLYWYLQKPGQSPQLLIYEVS
			NRFSGVPDRFSGSGSGTDFTLKISRVEAEDVGVYYCMQS
			IQLPITFGQGTRLEIKRAA [Seq ID 41]
mix7	MCF7	mixLIB	GAGCAGGTGCAGCTGGTGCAGTCTGGGGCGGAGGTGAAG
	cells		AAGCCTGGGGCCTCAGTGAGAGTTTCCTGCCAGGCATCT
			GGATACACATTCAGCAGGTACCATATGCACTGGGTGCGA
			CAGGCCCCTGGACAAGGGCTTGAGTGGATGGGAGTGATC
			GACCCCAATAGTGGTAGAGTAAGTTACTCACAGAAGTTC
			CAGGACAGAGTTACCATGACCAGGGACACGTCCACGAGC
			ACAGTATACATGGAGCTGAACAGCCCGAGATCTGAGGAC
			ACGGCCGTTTATTATTGTGCGAGAGATCGAGGATATTGT
			AATGGTGGCAGGTGCTTTATGGATGCATTTGACTACTGG
			GGCCAGGGGACAATGGTCACCGTCTCTTCAGGTGGAGGC
			GGTTTAGGCGGAGGTGGCTCTGGCGGTGGCGGATCGTCC
			TATGTGCTGACTCACCCACCCTCATTGTCTGGGGCCCCA
			GGGCAGAGCATCACCATCTCCTGCACTGGGAGCAGTTCC
			AACATCGGGGCAGGTTTTCATATACACTGGTACCAGCAG
			TTTCCAAAAACAGCCCCCAAACTCCTTATCTATGGTAGT
			AGTAATCGACCCTCAGGGGTCCCTGACCGCTTCTCTGGC
			TCCAGGTCTGGCTCCTCAGGCTCCCTGGCCATCACTGGG
			CTCCAGGCAGACGATGAGGCTGATTATTACTGTGTGGGA
			TGGGATGGCAGCCTGAGTGGTTATGTCTTCGGAACTGGG
			ACCCAGCTCACCGTTTTAGGTGCGGCCGCA [Seq ID 16]
			EQVQLVQSGAEVKKPGASVRVSCQASGYTFSRYHMHWVR
			QAPGQGLEWMGVIDPNSGRVSYSQKFQDRVTMTRDTSTS
			TVYMELNSPRSEDTAVYYCARDRGYCNGGRCFMDAFDYW
			GQGTMVTVSSGGGGLGGGGSGGGGSSYVLTHPPSLSGAP
			GQSITTSCTGSSSNIGAGFHIHWYQQFPKTAPKLLIYGS
			SNRPSGVPDRFSGSRSGSSGSLAITGLQADDEADYYCVG
			WDGSLSGYVFGTGTQLTVLGAAA [Seq ID 17]
mix8	MCF7	mixLIB	GAGCAGGTGCAGCTGGTGCAGTCTGGGGGAGGCGTGGTC
	cells		CAGCCTGGGAGGTCCCTGAGACTCTCCTGTGCAGCCTCT
			GGATTCAGCTTCAGTAACTATGTTATGCACTGGGTCCGC
			CAGGCTCCAGGCAAGGGGCTGGAGTGGGTGGCAGTTATA
			TCACATGATGGAAGCAATAAATACTACGCAGACTCCGTG
			AAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAAC
			ACGCTATATCTGCAAATGAAAAGCCTGAGACCTGAGGAC
			ACGGCTGTGTATTACTGTGCGAGAAGTAGTGGCTGGTAC
			CTTCTCTTTGATGCTTTTGATATCTGGGGCCAAGGGACA
			ATGGTCACCGTCTCTTCAGGTGGAGGCGGTTCAGGCGGA
			GGTGGCTCTGGCGGTGGCGGATCGGACATCCAGATGACC
			CAGTCTCCAGACTCCCTGCCTGTGTCTCTGGGCGAGAGG
			GCCACCATCAACTGCAGGTCCAGCCAGAGTGTTTTATAC
			AGCTCCAACAATAAGAACTACTTAGCTTGGTACCAGCAG
			AAACCAGGACAGCCTCCTAAGCTGCTCATTTACTGGGCA
			TCTACCCGGGAATCCGGTGTCCCTGACCGATTCAGTGGC
			AGCGGGTCTGGGACAGATTTCACTCTCACCATCAGCAGC
			CTGCAGGCTGAAGATGTGGCAGTTTATTACTGTCAGCAA
			TATTATAGGATTCCGTGGACGTTCGGCCAAGGGACGAAG
			GTGGAAATCAAACGTGCGGCCGCA [Seq ID 42]
			EQVQLVQSGGGVVQPGRSLRLSCAASGFSFSNYVMHWVR
			QAPGKGLEWVAVISHDGSNKYYADSVKGRFTISRDNSEN
			TLYLQMKSLRPEDTAVYYCARSSGWYLLFDAFDIWGQGT
			MVTVSSGGGGSGGGGSGGGGSDIQMTQSPDSLPVSLGER
			ATINCRSSQSVLYSSNNKNYLAWYQQKPGQPPKLLIYWA
			STRESGVPDRFSGSGSGTDFTLTISSLQAEDVAVYYCQQ
			YYRIPWTFGQGTKVEIKRAAA [Seq ID 43]
mix11	MCF7	mixLIB	GAGGAGGTGCAGCTGTTGCAGTCTGGGGGAGGTGTGGTA
	cells		CGGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCCTCT
			GGATTCACCTTTGATGATTATGGCATGACCTGGGTCCGC
			CAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAGCTATT
			AGTGGTAGTGGTGGTAGCACATACTACGCAGACTCCGTG
			AAGGGCCGGTTCGCCATCTCCAGAGACAATTCCAAGAAC
			ACGCTGTATCTGCAAATGAACAGCCTGAGAGCCGAGGAC
			ACGGCCGTATATTACTGTGCGAAATCTCGCTACTATGAT
			AGTAGTGGTTATTACTACACCGTGCGACCTGATGCTTTT
			GATATCTGGGGCCAAGGGGCAATGGTCACCGTCTCTTCA
			GGTGGAGGCGGTGGAGGTGGCTCTGGCGGTGGCGGATCG
			TCTTCTGAGCTGACTCAACCACCCTCAGTGTCCGTGTCC
			CCAGGACAGACAGCCATCATCACCTGCTCTGGAGATAAA
			TTGGGGGATAAATATGCTTCCTGGTATCAGCACAGGCCA
			GGCCAGTCGCCTGTCTTGGTCATCTATCAGGATTCCAGG
			CGGCCCTCAGACATCCCTGAGCGATTCTCTGGCTCCAAC
			TCTGGGAACACAGCCACTCTGACCATCACCGAGGCCCAG
			GCTTTGGATGAGGCTGACTATTATTGTCAGGCCTGGGCC
			GGCAGATCTGTGGTCTTCGGCGGGGGGACCCAGCTCACC
			GTTTTAGGTGCGGCCGCA [Seq ID 44]
			EEVQLLQSGGGVVRPGGSLRLSCAASGFTFDDYGMTWVR
			QAPGKGLEWVSAISGSGGSTYYADSVKGRFAISRDNSEN
			TLYLQMNSLRAEDTAVYYCAKSRYYDSSGYYYTVRPDAF
			DIWGQGAMVTVSSGGGGGGGSGGGGSSSELTQPPSVSVS
			PGQTAIITCSGDKLGDKYASWYQHRPGQSPVLVIYQDSR
			RPSDIPERFSGSNSGNTATLTITEAQALDEADYYCQAWA
			GRSVVFGGGTQLTVLGAAA [Seq ID 45]
mix12	MCF7	mixLIB	GAGGAGGTGCAGCTGTTGCAGTCTGGGGCGGAGGTGAAG
	cells		AAGCCTGGGGCCTCAGTGAGAGTTTCCTGCCAGGCATCT
			GGATACACATTCAGCAGGTACCATATGCACTGGGTGCGA
			CAGGCCCCTGGACAAGGCCTTGAGTGGATGGGAGTGATC
			GACCCCAATAGTGGTAGAGTAAGTTACTCACAGAAGTTC
			CAGGACAGAGTCACCATGACCAGGGACACGTTCACGAGC
			ACAGTATACATGGAGCTGAACAGCCTGAGATCTGAGGAC
			ACGGCCGTTTATTATTGTGCGAGAGATCGAGGATATTGT
			AATGGTGGCAGGTGCTTTATGGATGCATTTGACTACTGG
			GGCCAGGGGACCACGGTCACCGTCTCCTCAGGTGGAGGC
			GGTTCAGGCGGAGGTGGCCCTGGCGGTGGCGGATCGTCC
			TATGTGCTGACTCAGCCACCCTCAGCGTCTGGGGCCCCC
			GGACAGAGGGTCACCATCTCTTGTTCTGGAAGCAACTCC
			AACATCGGACGTAATTGGGTATACTGGTACCAGCAACTC
			CCAGGAACGGCCCCCAAACTCCTCATGTTTAGGAATAAT
			GAACGGTCCTCAGGGGTCCCTGACCGATTCTCTGGCTCC
			AAGACTGGCACCTCAGCCTCCCTGGCCATCAGTGGGCTC
			CGGTCTGAGGATGAGGGTGATTACTACTGTGCATCATGG
			GATGACAGTCTGCATGCTTGGGTGTTCGGCGGGGGGACC
			CAGCTCACCGTTTTAGGTGCGGCCGCA [Seq ID 46]
			EEVQLLQSGAEVKKPGASVRVSCQASGYTFSRYHMHWVR
			QAPGQGLEWMGVIDPNSGRVSYSQKFQDRVTMTRDTFTS
			TVYMELNSLRSEDTAVYYCARDRGYCNGGRCFMDAFDYW
			GQGTTVTVSSGGGGSGGGGPGGGGSSYVLTQPPSASGAP
			GQRVTISCSGSNSNIGRNWVYWYQQLPGTAPKLLMFRNN
			ERSSGVPDRFSGSKTGTSASLAISGLRSEDEGDYYCASW
			DDSLHAWVFGGGTQLTVLGAAA [Seq ID 47]
mix17	MCF7	mixLIB	GAGCAGGTGCAGCTGGTGCAGTCTGGGGGAGGCTTGGTA
	cells		CAGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCCTCT
			GGATTCACCTTTAGCAGCTATGCCATGAGCTGGGTCCGC
			CAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAGCTATT
			AGTGGTAGTGGTGGTAGCACATACTACGCAGACTCCGTG
			AAGGGCCGGTTCACCATCTCCAGAGAGAATTCCAAGAAC
			ACGCTATATCTGCAAATGAATAGCCTGAGAGCCGAGGAC
			ACGGCTGTGTATTACTGTGCGAGACAAACAAGAGTCCGT
			GCTTTTGATATCTGGGGCCAAGGGACAATGGTCACCGTC
			TCTTCAGGTGGAGGCGGTTCAGGCGGAGGTGGCTCTGGC
			GGTGGCGGATCGGACATCCAGATGACCCAGTCTCCTTCC
			GCCCTGTCTGCATCTGTAGGAGGCAGAGTCACCATCACT
			TGCCGGGCAAGTCAGAGCACTAGTAGCGATTTAAATTGG
			TATCAGCAAAGACCAGGGAAAGCCCCTAAACTCCTGATC
			TCTGTTGCATCCACTTTACAAAGTGACGTCCCATCAAGG
			TTCAGTGGCAGTGGTTCTGGGACAGATTTCAGTCTCACC
			ATCAGCAGTCTGCAACCTGAAGACTTTGCAACTTACTTC
			TGTCAACAGAGTTACAGCACCCCGTACACTTTTGGCCAG
			GGGACCAAAGTGGATATCAAACGTGCGGCCGCA [Seq
			ID 18]
			EQVQLVQSGGGLVQPGGSLRLSCAASGFTFSSYAMSWVR
			QAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRENSEN
			TLYLQMNSLRAEDTAVYYCARQTRVRAFDIWGQGTMVTV
			SSGGGGSGGGGSGGGGSDIQMTQSPSALSASVGGRVTIT
			CRASQSTSSDLNWYQQRPGKAPKLLISVASTLQSDVPSR
			FSGSGSGTDFSLTISSLQPEDFATYFCQQSYSTPYTFGQ
			GTKVDIKRAAA [Seq ID 19]
mix23	MCF7	mixLIB	GAGGAGGTGCAGCTGGTGGAGTCTGGGGGAAACTTGGTT
	cells		CAGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCCTCT
			GGATTCACCTTTAGCAGTTATGCCATGAGCTGGGTCCGC
			CAGGCTCCAGGGAAGGGGCTGGAATGGGTCTCAGCTATT
			AGTGCTAGTGGTGGCACCACATACTACGCAGATTCCGTG
			AAGGGCCGGTTCACCATCTCCAGAGACAATTCCAAGAAC
			ACGCTGTATCTTCAAATGAACAGCCTGAGAACTGAGGAC
			ACGGCTGTGTATTACTGTGCGAGAGACAGCCGTGCATAC
			AGCTATGGTTACCTCTACGTCTTTGACTACTGGGGCCAG
			GGCACCCTGGTCACCGTCTCCTCAGGTGGAGGCGGTTCA
			GGCGGAGGTGGCTCTGGCGGTGGCGGATCGCAGTCTGCC
			CTGACTCAGCCTGCCTCCGTGTCTGGGTCTCCTGGACAG
			TCGATCACCATCTCCTGCACTGGAACCAGCAATGATGTT
			GGGAGTTATAACCTTGTCTCCTGGTACCAACAACACCCA
			GGCAAAGCCCCCAAACTCCTGATTTATGAGGGCAGTAAG
			CGGCCCTCAGGGATTTCTAATCGCTTCTCTGGCTCCAAG
			TCTGGCAACACGGCCTCCCTGACCATCTCTGGGCTCCAG
			GCTGAGGACGAGGCTGATTATTACTGCATGTCATATACG
			AGCAGTGGCACTCCTTATGTCTTCGGAACTGGGACCCAG
			CTCACCGTTTTAGGTGCGGCCGCA [Seq ID 48]
			EEVQLVESGGNLVQPGGSLRLSCAASGFTFSSYAMSWVR
			QAPGKGLEWVSAISASGGTTYYADSVKGRFTISRDNSEN
			TLYLQMNSLRTEDTAVYYCARDSRAYSYGYLYVFDYWGQ
			GTLVTVSSGGGGSGGGGSGGGGSQSALTQPASVSGSPGQ
			SITISCTGTSNDVGSYNLVSWYQQHPGKAPKLLIYEGSK
			RPSGISNRFSGSKSGNTASLTISGLQAEDEADYYCMSYT
			SSGTPYVFGTGTQLTVLGAAA [Seq ID 49]
mix25	MCF7	mixLIB	GAGGAGGTGCAGCTGGTGGAGTCTGGGGCTGAGGTGAAG
	cells		AAGCCTGGGGCCTCAGTGAGAGTTTCCTGCCAGGCATCT
			GGATACACATTCACCAGGTACCATATACACTGGGTGCGA
			CAGGCCCCTGGACAAGGGCTTGAGTGGATGGGAGTGATC
			GACCCCAATAGTGGTAGAATAAGTTACTCACAGAAGTTC
			CAGGACAGAGTCACCATGACCAGGGACACGTCCACGAGC
			ACAGTCTACATGGAGCTGAACAGCCTGAGATCTGAGGAC
			ACAGCCATTTATTACTGTGCGAGAGATCGAGGATATTGT
			AATGGTGGCAGGTGCTTTATGGATGCATTTGACTACTGG
			GGCCAGGGGACCACGGTCACCGTCTCCTCAGGTGGAGGC
			GGTTCAGGCGGAGGTGGCTCTGGCGGTGGCGGATCGCAG
			TCTGTGTTGACGCAGCCGCCCTCAGCGTCTGGGACCCCC
			GGGCAGAGGGTCACCATCGCTTGTTCTGGAAGCAGCTCC
			AACATCGGAATTAATACTGTAAACTGGTACCAGCAGATC
			CCAGGAACGGCCCCCAAACTCCTCATCTATAATAATGAT
			CAGCGGCCCTCAGGGGTCCCTGACCGATTCTCTGGCTCC
			AAGTCTGCCACCTCAGCCTCCCTGGCCATCACTGGGCTC
			CAGGTTGACGATGAGGCTGATTATTACTGCCAGTCCTAT
			GACAGCAGCCTGGGTGGTTATGTCTTCGGAACTGGGACC
			CAGCTCACCGTTTTAGGTGCGCCCGCA [Seq ID 50]
			EEVQLVESGAEVKKPGASVRVSCQASGYTFTRYHIHWVR
			QAPGQGLEWMGVIDPNSGRISYSQKFQDRVTMTRDTSTS
			TVYMELNSLRSEDTAIYYCARDRGYCNGGRCFMDAFDYW
			GQGTTVTVSSGGGGSGGGGSGGGGSQSVLTQPPSASGTP
			GQRVTIACSGSSSNIGINTVNWYQQIPGTAPKLLIYNND
			QRPSGVPDRFSGSKSATSASLAITGLQVDDEADYYCQSY
			DSSLGGYVFGTGTQLTVLGAAA [Seq ID 51]
mix39	MCF7	mixLIB	GAGGAGGTGCAGCTGTTGCAGTCTGGGGGAGGCGTGGTC
	cells		CAGCCTGGGAGGTCCCTGAGACTCTCCTGTGCAGCCTCT
			GGATTCAGCTTCAGTAACTATGTTATGCACTGGGTCCGC
			CAGGCTCCAGGCAAGGGGCTGGAGTGGGTGGCAGTTATA
			TCATATGATGGAAGCAATAAATACTACGCAGACTCCGTG
			AAGGGCCGATTCACCATCTCCAGAGACAATTCCAAGAAC
			ACGCTATATCTGCAAATGAAAGGCCTGAGACCTGAGGAC
			ACGGCTGTGTATTACTGTGCGAGAAGTAGTGGCTGGTAC
			CTTCTCTTTGATGCTTTTGATATCTGGGGCCAAGGGACA
			ATGGTCACCGTCTCTTCAGGTGGAGGCGGTTCAGGCGGA
			GGTGGCTCTGGCGGTGGCGGATCGGATGTTGTGATGACA
			CAGTCTCCAGACTCCCTGGCTGTGTCGCTGGGCGAGAGG
			GCCACCATCAACTGCGAGTCCAGCCAGAGTGTTTTATTC
			AGCTCCAACAATAAGAACTACTTAGCTTGGTACCAGCAG
			AAACCAGGACAGCCTCCTAAGCTGCTCATTTACTGGGCA
			TCTACCCGGGAATCCGGGGTCCCTGACCGATTCAGTGGC
			AGCGGGTCTGAGACAGATTTCACTCTCACCATCAGCAGC
			CTGCAGGCTGAAGATGTGGCAGTTTATTACTGTCAGCAA
			TATTATAGGATTCCGTGGACGTTCGGCCAAGGGACCAAA
			GTGGATATCAAACGTGCGGCCGCA [Seq ID 20]
			EEVQLLQSGGGVVQPGRSLRLSCAASGFSFSNYVMHWVR
			QAPGKGLEWVAVISYDGSNKYYADSVKGRFTISRDNSEN
			TLYLQMKGLRPEDTAVYYCARSSGWYLLFDAFDIWGQGT
			MVTVSSGGGGSGGGGSGGGGSDVVMTQSPDSLAVSLGER
			ATINCESSQSVLFSSNNKNYLAWYQQKPGQPPKLLIYWA
			STRESGVPDRFSGSGSETDFTLTISSLQAEDVAVYYCQQ
			YYRIPWTFGQGTKVDIKRAAA [Seq ID 21]
B96/	MCF7	scFvB96	ATGGAGCAGGTGCAGCTGCAGGAGTCTGGGGGAGGCTTG
4F	cells		GTACAGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCC
			TCTGGATTCACCTTTAGTACTTATGCCATGAGCTGGGTC
			CGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAGTT
			ATTAGTGGTAGTGGTCATACAACAAACTACGCCGACTCC
			GTGAAGGGCCGCGTCACCATATCCAGAGACAATTCCAAG
			AACACACTATATCTGCAAATCAACAGCCTGAGAGCCGAC
			GACACGGCCGTGTATTACTGTGCGAGAGATGTGTTAGTC
			CTACAGAATGCTTTTGATATCTGGGGCCAAGGGACCACG
			GTCACCGTCTCCTCAGGTGGAGGTGGTTCAGGCGGAGGT
			GGCTCTGGCGGTGGCGGATCGGATGTTGTGATGACCCAG
			TCTCCATCCTCACTGTCTGCATCTGTAGGAGACAGAGTC
			ACCATCACTTGTCGGGCGAGTCAGGGTATTAGCAGGTGG
			TTAGCCTGGTATCAACAGAAACCAGGGAAAGCCCCTAAG
			CTCCTGATCTACGCTGCATCCAGTTTGCAAAGTGGGGTC
			CCATCAAGGTTCAGTGGCAGTGGATCTGGGACAGATTTC
			ACTCTCACCATCAGCAGTCTGCAACCTGAAGATTTTGCA
			ACTTACATCTGTCAACAGAGTTACAGTAGGCCGCTCACT
			TTCGGCGGAGGGACCAAGGTGGAAATCAAACGTGCGGCC
			GCA [Seq ID 52]
			MEQVQLQESGGGLVQPGGSLRLSCAASGFTFSTYAMSWV
			RQAPGKGLEWVSVISGSGHTTNYADSVKGRVTISRDNSK
			NTLYLQINSLRADDTAVYYCARDVLVLQNAFDIWGQGTT
			VTVSSGGGGSGGGGSGGGGSDVVMTQSPSSLSASVGDRV
			TITCRASQGISRWLAWYQQKPGKAPKLLIYAASSLQSGV
			PSRFSGSGSGTDFTLTISSLQPEDFATYICQQSYSRPLT
			FGGGTKVEIKRAAA [Seq ID 53]
B96/	MCF7	scFvB96	GAGCAGGTGCAGCTGCAGGAGTCTGGGGGAGGCTTGGTA
11L	cells		CAGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCCTCT
			GGATTCACCTTTAGTACTTATGCCATGAGCTGGGTCCGC
			CAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAGTTATT
			AGTGGTAGTGGTCATACAACAAACTACGCCGACTCCGTG
			AAGGGCCGCGTCACCATATCCAGAGACAATTCCAAGAAC
			ACACTATATCTGCAAATCAACAGCCTGAGAGCCGACGAC
			ACGGCCGTGTATTACTGTGCGAGAGATGTGTTAGTCCTA
			CAGAATGCTTTTGATATCTGGGGCCAAGGGACCACGGTC
			ACCGTCTCCTCAGGTGGAGGTGGTTCAGGCGGAGGTGGC
			TCTGGCGGTGGCGGATCGGATGTTGTGATGACCCAGTCT
			CCATCCTCACTGTCTGCATCTGTAGGAGACAGAGTCACC
			ATCACTTGTCGGGCGAGTCAGGGTATTAGCAGGTGGTTA
			GCCTGGTATCAACAGAAACCAGGGAAAGCCCCTAAGCTC
			CTGATCTACGCTGCATCCAGTTTGCAAAGTGGGGTCCCA
			TCAAGGTTCAGTGGCAGTGGATCTGGGACAGATTTCACT
			CTCACCATCAGCAGTCTGCAACCTGAAGATTTTGCAACT
			TACATCTGTCAACAGAGTTACAGTAGGCCGCTCACTTTC
			GGCGGAGGGACCAAGGTGGAAATCAAACGTGCGGCCGCA
			[Seq ID 14]
			EQVQLQESGGGLVQPGGSLRLSCAASGFTFSTYAMSWVR
			QAPGKGLEWVSVISGSGHTTNYADSVKGRVTISRDNSEN
			TLYLQINSLRADDTAVYYCARDVLVLQNAFDIWGQGTTV
			TVSSGGGGSGGGGSGGGGSDVVMTQSPSSLSASVGDRVT
			ITCRASQGISRWLAWYQQKPGKAPKLLIYAASSLQSGVP
			SRFSGSGSGTDFTLTISSLQPEDFATYICQQSYSRPLTF
			GGGTKVEIKRAAA [Seq ID 15]

TABLE 6
Kinetic values of parental and affinity maturated single-chain antibodies.
Parental anti-CEA antibody CB37 is not stable in soluble form. Maturated
single-chain antibodies have nanomolar affinity. Ka = association
constant, Kd = dissociation constant, KD = Ka/
Kd, SE = standard error. Data are expressed in Molar.
scFV	ka (+/−SE)	kd (+/−SE)	KD
MB5	2.13E+04 (2.45E+02)	8.55E−03 (6.25E−05)	4.01E−07
MBB5/C′1	1.53E+05 (4.15E+02)	1.45E−03 (1.29E−05)	9.46E−09
MB5/C′3	7.11E+04 (4.33E+02)	1.64E−03 (2.46E−05)	2.31E−08
CB37	—	—	—
CB37/3B	1.27E+05 (9.79E+02)	1.42E−04 (3.23E−05)	3.66E−09
CB37/9C	1.00E+05 (5.75E+02)	4.65E−04 (2.54E−05)	1.42E−09

This study with Biacore provided quantitative measures of scFv-antigen binding and dissociation kinetics. Table 6 reports the kinetic values of the parental and affinity-maturated scFvs. The maturated antiMUC1 antibodies MB5/C′1 and MB5/C′3 have over 42 times and 17 times higher affinity to the antigen, compared to MB5, respectively. The maturated anti-CEA antibodies CB37/3B and CB37/9C have nanomolar affinity. Moreover, the maturated antibodies are more stable than original CB37, which was not reactive in soluble form. These results indicate that pKM19 vector is a suitable tool for maturation of scFv antibodies.

SEQUENCE LISTING

<160> NUMBER OF SEQ ID NOS: 102

<210> SEQ ID NO 1

<211> LENGTH: 3770

<212> TYPE: DNA

<213> ORGANISM: Escherichia coli

<400> SEQUENCE: 1

gcccaatacg caaaccgcct ctccccgcgc gttggccgat tcattaatgc agctggcacg 60

acaggtttcc cgactggaaa gcgggcagtg agcgcaacgc aattaatgtg agttagctca 120

ctcattaggc accccaggct ttacacttta tgcttccggc tcgtatgttg tgtggaattg 180

tgagcggata acaatttcac acaagatcta gctattctag agattacgcc aagccccgta 240

ttttacccgt ttaatggaag cttataaagg aggaaatcct catgaaatag agcaccatcg 300

cactggcact gttaccgtta ctgttcaccc cggttaccaa agcacgtacc atggtttccc 360

ttgcggccgc aggagactac aaagacgacg acgacaaaga attcctgcct caacctcctg 420

tcaatgctgg cggcggctct ggtggtggtt ctggtggcgg ctctgagggt ggcggctctg 480

<400> SEQUENCE: 102

gctgaggaga cggtgacc

Claims

1. An isolated or purified vector suitable for efficient selection and affinity maturation of a recombinant antibody, the recombinant antibody having a leader peptide and being encoded by a recombinant antibody coding sequence, wherein

the vector comprises a leader sequence encoding a leader peptide expressed with the recombinant antibody,

the vector further comprising at least one element able to reduce the expression level of said recombinant antibody, the at least one element being selected from

a) a suppressed stop codon inside either the leader peptide or the recombinant antibody coding sequence;

b) a low-efficient promoter driving transcription of said recombinant antibody coding sequence; or

c) an inhibitor of the promoter driving transcription of said recombinant antibody coding sequence; and

2. The vector according to claim 1 wherein the recombinant antibody includes: ScFv, active fragments of Abs, or humanized sequences of Abs.

3. The vector according to claim 1 wherein the vector is a plasmid, a phagemid or a phage.

4. The vector according to claim 1, said vector being a phagemid vector having the nucleotide sequence of SEQ ID NO: 1.

5. An in vitro host cell transformed with the vector according to claim 1.

6. A non-human host cell transformed with the vector according to claim 1.

7. The non-human host cell of claim 6, wherein the non-human host cell is a bacterial cell.

8. The vector of claim 1, wherein the vector is a DNA vector.

9. The in vitro host cell of claim 5, wherein the host cell is a bacterial cell.

10. A method for improving selection and/or maturation of a recombinant antibody, the method comprising

cloning and expressing sequences encoding for recombinant antibodies with the vector according to claim 1; and

selecting a cloned and expressed recombinant antibody having an affinity for an antigen or target protein thus improving the selection and/or maturation of the recombinant antibody.

11. The method of claim 10, wherein the cloning and expressing comprises

constructing a phage display library for the recombinant antibody with the vector of claim 1 comprising the sequences encoding for the recombinant antibodies.

12. The method of claim 11, wherein the phage display library is selected from a synthetic or semi-synthetic antibody library, or a library mutated for affinity maturation of antibodies.

13. The method of claim 11, wherein the selecting comprises

performing affinity selection of the recombinant antibodies from the phage display library to obtain an affinity selected recombinant antibody having high affinity for the antigen or target protein.

14. The method of claim 11, wherein the phage display library -is a library mutated for affinity maturation of antibodies; and the selecting comprises

selecting a maturated recombinant antibody from the library mutated for affinity maturation of antibodies, the maturated recombinant antibody having an affinity for an antigen or target protein.

15. The method of claim 11, wherein the phage display library is a library mutated for affinity maturation of antibodies; and the selecting comprises

performing affinity selection of maturated recombinant antibodies from the library mutated for affinity maturation of antibodies to obtain an affinity maturated recombinant antibody having high affinity for an antigen or a target protein.

16. The method of claim 10, wherein the antigen or target protein is displayed on a cell.

17. The method of claim 10, wherein the sequences encoding for the recombinant antibodies comprise mutagenized sequences from an original sequence encoding for an original recombinant antibody.

18. The method of claim 10, wherein the sequences encoding for recombinant antibodies are derived from antibody producing cells.

19. The method of claim 18, wherein the antibody producing cells are Tumor Infiltrating Lymphocytes (TILs) or Peripheral Blood Lymphocytes (PBLs).

20. The method of claim 18, wherein the antibody producing cells are isolated from a tumor affected subject.

21. The method of claim 20, wherein the tumor affected subject is a breast cancer affected subject.