Inoue T, Asano Y, Matsuoka S, Furutani-Seiki M, Aizawa S, Nishimura H, Shirai T, Tada T
Department of Immunology, Faculty of Medicine, University of Tokyo, Japan.
J Immunol. 1993 Mar 15;150(6):2121-8.
Mouse CD8+ T cell clones could be subdivided into two subgroups by the pattern of cytokine production and CD45 isoforms that exactly corresponded with the functionally assigned cytotoxic (CTL) and suppressor (Ts) subsets. All the Ts clones invariably produced IL-10 after stimulation with immobilized anti-CD3, whereas none of CTL clones expressed mRNA of IL-10 by the same stimulation. All the CTL clones were positive for CD45RA Ag, a product of exon 4 of CD45 gene, whereas none of the Ts clones were positive for this Ag. The results are analogous to the situation within CD4+ T cell clones in which Th1 and Th2 subtypes can be distinguished by CD45 isoforms and cytokines they produce. Ts clones could suppress the proliferative responses of both Th1 and Th2 type CD4+ clones by the production of two different cytokines, IL-10 and IFN gamma, respectively, but none of the CTL clones could suppress the proliferation of CD4+ T cells. The participation of an additional nonspecific molecule in the suppression of antibody response is suggested.
小鼠CD8 + T细胞克隆可根据细胞因子产生模式和CD45异构体细分为两个亚组,这与功能上确定的细胞毒性(CTL)和抑制性(Ts)亚组完全对应。所有Ts克隆在用固定化抗CD3刺激后均能持续产生IL-10,而相同刺激下CTL克隆均不表达IL-10的mRNA。所有CTL克隆对CD45RA抗原呈阳性,CD45RA抗原是CD45基因第4外显子的产物,而所有Ts克隆对该抗原均呈阴性。这些结果类似于CD4 + T细胞克隆中的情况,其中Th1和Th2亚型可通过CD45异构体及其产生的细胞因子来区分。Ts克隆可分别通过产生两种不同的细胞因子IL-10和IFNγ来抑制Th1和Th2型CD4 +克隆的增殖反应,但CTL克隆均不能抑制CD4 + T细胞的增殖。提示存在另一种非特异性分子参与抗体反应的抑制。