Kay J E, Kromwel L, Doe S E, Denyer M
School of Biological Sciences, University of Sussex, Brighton, U.K.
Immunology. 1991 Apr;72(4):544-9.
The immunosuppressive macrolide rapamycin shows marked structural similarity to FK-506, and like FK-506 inhibits the activation of cultured T and B lymphocytes at concentrations as low as 10(-10) M. However, rapamycin blocks T-lymphocyte proliferation at a much later stage than FK-506. It also inhibits human, porcine and murine T- and B-lymphocyte activation by all pathways tested, including pathways which are insensitive to FK-506, such as interleukin-2 (IL-2)-mediated proliferation of IL-2-dependent T-cell lines, activation of human peripheral blood T lymphocytes by phorbol ester and anti-CD28 and activation of murine B lymphocytes by bacterial lipopolysaccharide. Thus these two macrolides that bind competitively to the same major intracellular receptor protein inhibit T- and B-lymphocyte activation by quite distinct mechanisms.
免疫抑制性大环内酯类药物雷帕霉素与FK-506在结构上有显著相似性,并且与FK-506一样,在低至10(-10)M的浓度下就能抑制培养的T淋巴细胞和B淋巴细胞的激活。然而,雷帕霉素阻断T淋巴细胞增殖的阶段比FK-506要晚得多。它还通过所有测试途径抑制人、猪和鼠的T淋巴细胞和B淋巴细胞激活,包括对FK-506不敏感的途径,如白细胞介素-2(IL-2)介导的IL-2依赖性T细胞系增殖、佛波酯和抗CD28对人外周血T淋巴细胞的激活以及细菌脂多糖对鼠B淋巴细胞的激活。因此,这两种竞争性结合同一主要细胞内受体蛋白的大环内酯类药物通过截然不同的机制抑制T淋巴细胞和B淋巴细胞的激活。