BISPECIFIC ANTIBODIES AND TARGETED CELLULAR CYTOTOXICITY
被引:57
作者:
FANGER, MW
论文数: 0引用数: 0
h-index: 0
机构:NCI,EXPTL IMMUNOL BRANCH,BETHESDA,MD 20892
FANGER, MW
SEGAL, DM
论文数: 0引用数: 0
h-index: 0
机构:NCI,EXPTL IMMUNOL BRANCH,BETHESDA,MD 20892
SEGAL, DM
ROMETLEMONNE, JL
论文数: 0引用数: 0
h-index: 0
机构:NCI,EXPTL IMMUNOL BRANCH,BETHESDA,MD 20892
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.