Kane K, Clark W R
J Immunol. 1984 Dec;133(6):2857-63.
The generation of CTL function by agents such as lectins, oxidative chemicals, or serum components has been regarded as independent of class I MHC products, because the CTL thus generated are able to lyse virtually any allogeneic target. However, we show here that CTL activation by lectin requires interaction of the pre-CTL with a class I MHC product on the lectin-presenting cell. The lectin-presenting cell can be an irradiated syngeneic or allogeneic spleen cell or, alternatively, lectin can be seen on a neighboring pre-CTL. In either case, there is an absolute requirement for simultaneous (although probably unlinked) perception of a class I MHC product. These results suggest that restricted clonal CTL activation by antigen, and polyclonal activation by so-called "nonspecific" mitogenic agents, may proceed through similar if not identical pathways.
诸如凝集素、氧化性化学物质或血清成分等因子所产生的细胞毒性T淋巴细胞(CTL)功能,一直被认为与I类主要组织相容性复合体(MHC)产物无关,因为如此产生的CTL实际上能够裂解任何异基因靶细胞。然而,我们在此表明,凝集素激活CTL需要前CTL与凝集素呈递细胞上的I类MHC产物相互作用。凝集素呈递细胞可以是经辐照的同基因或异基因脾细胞,或者,凝集素也可以出现在相邻的前CTL上。在任何一种情况下,都绝对需要同时(尽管可能不连锁)识别I类MHC产物。这些结果表明,抗原介导的限制性克隆CTL激活以及所谓“非特异性”促有丝分裂剂介导的多克隆激活,可能通过相似(如果不是相同)的途径进行。