BISPECIFIC ANTIBODIES AND TARGETED CELLULAR CYTOTOXICITY

被引:57
作者
FANGER, MW
SEGAL, DM
ROMETLEMONNE, JL
机构
[1] NCI,EXPTL IMMUNOL BRANCH,BETHESDA,MD 20892
[2] CTR NATL TRANSFUS SANGUINE,F-91943 LES ULIS,FRANCE
来源
IMMUNOLOGY TODAY | 1991年 / 12卷 / 02期
关键词
D O I
10.1016/0167-5699(91)90156-N
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Second International Conference on Bispecific Antibodies (BsAbs) and Targeted Cellular Cytotoxicity* considered how targeted cytotoxicity can be used (1) to increase understanding of the general mechanisms of cellular cytotoxicity and (2) clinically in the treatment of cancer and infections disease. BsAbs, the main mediators of targeted cellular cytotoxicity, can be made by chemical crosslinking, by fusing hybridoma cells and by molecular genetic approaches. BsAbs bind to target cells via one V region and trigger molecules such as T-cell receptors (TCRs) or FcR for IgG (Fc-gamma-R) on cytotoxic cells via their other V region. This linking of triggering structures to target cells induces target cells lysis and provides important clues to the signals used to elicit the lytic process.
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页码:51 / 54
页数:4
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