Groux H, Bigler M, de Vries J E, Roncarolo M G
Immunobiology Department, DNAX Research Institute of Molecular Immunology and Cellular Biology, Palo Alto, CA 94304, USA.
J Immunol. 1998 Apr 1;160(7):3188-93.
IL-10 is a well-documented immunosuppressant that inhibits macrophage-dependent Ag presentation and CD4+ T cell proliferation in vitro. We report that IL-10 inhibits alloantigen-specific proliferative responses and induces a long lasting anergic state in human purified CD8+ T cells when added concomitantly with the Ag in the presence of APC. Moreover, the generation of allospecific cytotoxic activity is inhibited by IL-10. These effects are indirect and are mediated through inhibition of the costimulatory functions of APC. In contrast, IL-10 has no direct inhibitory effects on the proliferation of purified CD8+ T cells activated by anti-CD3 mAb and promotes the growth of activated CD8+ T cells in combination with low doses of IL-2. Taken together, these results indicate that IL-10 has differential effects on CD8+ T cells depending on their state of activation, which may explain both the enhancing and inhibitory effects observed after IL-10 treatment in different in vivo experimental models.
白细胞介素-10(IL-10)是一种有充分文献记载的免疫抑制剂,在体外可抑制巨噬细胞依赖性抗原呈递及CD4+ T细胞增殖。我们报告称,当在抗原呈递细胞(APC)存在的情况下与抗原同时添加时,IL-10可抑制同种异体抗原特异性增殖反应,并在人纯化CD8+ T细胞中诱导持久的无反应状态。此外,IL-10可抑制同种特异性细胞毒性活性的产生。这些效应是间接的,通过抑制APC的共刺激功能介导。相比之下,IL-10对由抗CD3单克隆抗体激活的纯化CD8+ T细胞的增殖没有直接抑制作用,并且与低剂量IL-2联合使用时可促进活化CD8+ T细胞的生长。综上所述,这些结果表明IL-10对CD8+ T细胞的影响因其激活状态而异,这可能解释了在不同体内实验模型中IL-10治疗后观察到的增强和抑制作用。