Anti-idiotypic antibodies induced by genetic immunisation are directed exclusively against combined VL/VH determinants

被引:19
作者
Benvenuti, F [1 ]
Burrone, OR [1 ]
机构
[1] Int Ctr Genet Engn & Biotechnol, I-34012 Trieste, Italy
关键词
anti-idiotypic antibodies; DNA vaccination; lymphoma immunotherapy;
D O I
10.1038/sj.gt.3301546
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA vaccines encoding the idiotype of immunoglobulins of tumour B cells were shown to induce protection in several mouse lymphoma models. The mechanism of rejection of tumour cells has not been fully understood, but there is strong evidence suggesting that engagement of the idiotype by anti-idiotypic antibodies may directly result in inhibition of tumour growth. In this study, we have investigated the structural basis of the idiotypic/anti-idiotypic interaction following immunisation with DNA vaccines. scFvs containing only one of the two tumour-derived V regions recombined to an irrelevant V region partner were generated. These constructs encoding a secretory form of the scFv were used as immunogens to induce anti-ld antibodies. The same scFvs were expressed as membrane-bound molecules on the surface of mammalian cells. Analysis of immune sera on the membrane-displayed idiotypes revealed that DNA immunisation induced a polyclonal antibody response restricted to conformational combined epitopes formed by the parental V-L/V-H association. Immune sera raised by scFv DNA vaccination did not show any detectable reactivity towards chimeric scFvs containing only one of the two immunising V regions, indicating that the response against combined V-L/V-H determinants is highly dominant. Remarkably, the same immunogen, delivered as scFv protein, induced antibodies also directed against chain-specific determinants. These findings indicate that presentation of properly folded idiotypes results in a highly specific antibody response directed exclusively to private idiotypic determinants of the V-L/V-H combination of the immunogen.
引用
收藏
页码:1555 / 1561
页数:7
相关论文
共 29 条
[1]   Characterization of a second secreted IgE isoform and identification of an asymmetric pathway of IgE assembly [J].
Batista, FD ;
Efremov, DG ;
Burrone, OR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) :3399-3404
[2]   The two membrane isoforms of human IgE assemble into functionally distinct B cell antigen receptors [J].
Batista, FD ;
Anand, S ;
Presani, G ;
Efremov, DG ;
Burrone, OR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (06) :2197-2205
[3]   Anti-idiotypic DNA vaccines for lymphoma immunotherapy require the presence of both variable region genes for tumor protection [J].
Benvenuti, F ;
Burrone, OR ;
Efremov, DG .
GENE THERAPY, 2000, 7 (07) :605-611
[4]  
BESTAGNO M, 2001, IN PRESS BIOCHEMISTR
[5]  
CAMPBELL MJ, 1987, J IMMUNOL, V139, P2825
[6]   Analysis of the interaction of monoclonal antibodies with surface IgM on neoplastic B-cells [J].
Cragg, MS ;
Zhang, L ;
French, RR ;
Glennie, MJ .
BRITISH JOURNAL OF CANCER, 1999, 79 (5-6) :850-857
[7]   Setting the standards: Quality control in the secretory pathway [J].
Ellgaard, L ;
Molinari, M ;
Helenius, A .
SCIENCE, 1999, 286 (5446) :1882-1888
[8]  
ELLIOTT TJ, 1987, J IMMUNOL, V138, P981
[9]   MONOCLONAL-ANTIBODIES RAISED AGAINST THE IDIOTYPE OF THE MURINE B-CELL LYMPHOMA, BCL1 ACT PRIMARILY WITH HEAVY-CHAIN DETERMINANTS [J].
GEORGE, AJT ;
MCBRIDE, HM ;
GLENNIE, MJ ;
SMITH, LJ ;
STEVENSON, FK .
HYBRIDOMA, 1991, 10 (02) :219-227
[10]  
GEORGE AJT, 1988, J IMMUNOL, V141, P2168