Anti-idiotypic antibody as the surrogate antigen for cloning scFv and its fusion proteins

被引:7
作者
Cheung, NKV [1 ]
Guo, HF [1 ]
Modak, S [1 ]
Cheung, IY [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10021 USA
来源
HYBRIDOMA AND HYBRIDOMICS | 2002年 / 21卷 / 06期
关键词
D O I
10.1089/153685902321043963
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Single-chain variable fragment (ScFv) is a versatile building block for novel targeting constructs. However, a reliable screening and binding assay is often the limiting step for antigens that are difficult to clone or purify. Anti-idiotypic antibodies may be useful as surrogate antigens for cloning scFv and their fusion proteins. 8119 is a murine IgG(1) monoclonal antibody (MAII) specific for a novel antigen expressed on the cell surface of a wide spectrum of human solid tumors, but not in normal tissues. Rat anti-8H9-idiotypic hybridomas (clones 2E9, 1E12, and 1F11) were produced by somatic cell fusion between rat lymphocytes and mouse SP2/0 myeloma. In direct binding assays enzyme-linked immunosorbant assay-(ELISA)-they were specific for the 8119 idiotope. Using 2E9 as the surrogate antigen, 8H9-scFv was cloned from hybridoma cDNA by phage display. 8H9scFv was then fused to human-gamma1-CH2-CH3 cDNA for transduction into CHO and NSO cells. High expressors of mouse scFv-human Fc chimeric antibody were selected. The secreted homodimer reacted specifically with antigen-positive tumor cells by ELISA and by flow cytometry, inhibitable by the anti-idiotypic antibody. The reduced size resulted in a shorter half-life in vivo, while achieving comparable tumor to nontumor ratio as the native antibody 8H9. However, its in vitro activity in antibody-dependent cell-mediated cytotoxicity was modest.
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页码:433 / 443
页数:11
相关论文
共 38 条
[11]   APPLICATIONS OF MONOCLONAL-ANTIBODIES IN CLINICAL ONCOLOGY [J].
GEORGE, AJT ;
SPOONER, RA ;
EPENETOS, AA .
IMMUNOLOGY TODAY, 1994, 15 (12) :559-561
[12]   Homodimerization of tumor-reactive monoclonal antibodies markedly increases their ability to induce growth arrest or apoptosis of tumor cells [J].
Ghetie, MA ;
Podar, EM ;
Ilgen, A ;
Gordon, BE ;
Uhr, JW ;
Vitetta, ES .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) :7509-7514
[13]   Isolation of single chain antibody fragments with specificity for cell surface antigens by phage display utilizing internal image anti-idiotypic antibodies [J].
Hombach, A ;
Pohl, C ;
Heuser, C ;
Sircar, R ;
Diehl, V ;
Abken, H .
JOURNAL OF IMMUNOLOGICAL METHODS, 1998, 218 (1-2) :53-61
[14]   PROTEIN ENGINEERING OF ANTIBODY-BINDING SITES - RECOVERY OF SPECIFIC ACTIVITY IN AN ANTI-DIGOXIN SINGLE-CHAIN FV ANALOG PRODUCED IN ESCHERICHIA-COLI [J].
HUSTON, JS ;
LEVINSON, D ;
MUDGETTHUNTER, M ;
TAI, MS ;
NOVOTNY, J ;
MARGOLIES, MN ;
RIDGE, RJ ;
BRUCCOLERI, RE ;
HABER, E ;
CREA, R ;
OPPERMANN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (16) :5879-5883
[15]   Mammalian expression of single chain variable region fragments dimerized by Fc regions [J].
Kato, T ;
Sato, K ;
Suzuki, S ;
Sasakawa, T ;
Kurokawa, M ;
Nishioka, K ;
Yamamoto, K .
MOLECULAR BIOLOGY REPORTS, 1995, 21 (03) :141-146
[16]  
Kipriyanov Sergey M., 1995, Human Antibodies and Hybridomas, V6, P93
[17]   HUMAN ANTI-IDIOTYPE ANTIBODIES IN CANCER-PATIENTS - IS THE MODULATION OF THE IMMUNE-RESPONSE BENEFICIAL FOR THE PATIENT [J].
KOPROWSKI, H ;
HERLYN, D ;
LUBECK, M ;
DEFREITAS, E ;
SEARS, HF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (01) :216-219
[18]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[19]   An alternating selection strategy for cloning phage display antibodies [J].
Lu, J ;
Sloan, SR .
JOURNAL OF IMMUNOLOGICAL METHODS, 1999, 228 (1-2) :109-119
[20]   In vitro and in vivo characterisation of a recombinant carboxypeptidase G(2)::anti-CEA scFv fusion protein [J].
Michael, NP ;
Chester, KA ;
Melton, RG ;
Robson, L ;
Nicholas, W ;
Boden, JA ;
Pedley, RB ;
Begent, RHJ ;
Sherwood, RF ;
Minton, NP .
IMMUNOTECHNOLOGY, 1996, 2 (01) :47-57