Palacios R
J Clin Immunol. 1982 Jul;2(3 Suppl):15S-19S.
Cyclosporin-A strongly suppressed proliferation of T cells induced by the OKT3 monoclonal antibody when added at the beginning of the cultures but not when added 72 hr later. The inhibitory activity of Cyclosporin-A became apparent during the first 48 hr and was maintained throughout the culture period. Cyclosporin-A significantly inhibited binding of OKT3, but not OKT4 or OKT8, antibodies to T cells as determined by indirect immunofluorescence microscopy. In addition, Cyclosporin-A suppressed the killing of 51Cr labelled T cells mediated by OKT3 antibody plus complement, whereas Cyclosporin-A did not alter the lysis of T cells by OKT4 antibody plus complement treatment. These results strongly suggest that Cyclosporin-A and OKT3 antibody exert their respective suppressive and mitogenic activity on T cells by interacting with the same receptor.
环孢素A在培养开始时添加能强烈抑制由OKT3单克隆抗体诱导的T细胞增殖,但在72小时后添加则无此作用。环孢素A的抑制活性在最初48小时内明显,并在整个培养期持续存在。通过间接免疫荧光显微镜检查确定,环孢素A显著抑制OKT3抗体与T细胞的结合,但不抑制OKT4或OKT8抗体与T细胞的结合。此外,环孢素A抑制OKT3抗体加补体介导的51Cr标记T细胞的杀伤作用,而环孢素A不改变OKT4抗体加补体处理对T细胞的裂解作用。这些结果强烈表明,环孢素A和OKT3抗体通过与同一受体相互作用,对T细胞发挥各自的抑制和促有丝分裂活性。