Fazekas de St Groth B, Gallagher P F, Miller J F
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2594-8. doi: 10.1073/pnas.83.8.2594.
The murine T-cell surface molecules Lyt-2 and L3T4 play a role in the activation of antigen-specific T cells. The currently accepted model for the function of these molecules proposes that Lyt-2 and L3T4 increase the overall avidity of the interaction between the T-cell antigen receptor and antigen in association with the major histocompatibility complex (MHC) molecules on the antigen-presenting cell. We have used two unusual Lyt-2+ L3T4+ class II MHC-restricted T-cell clones to test whether Lyt-2 can substitute for L3T4 when the T-cell antigen receptor is class II MHC-restricted. Monoclonal antibodies against L3T4 profoundly inhibited antigen-induced lymphokine production by both T-cell clones. Anti-Lyt-2 monoclonal antibody had no effect. These results strongly suggest that L3T4 and the class II-restricted T-cell antigen receptors are physically close during antigen recognition, probably as part of a multimolecular complex from which Lyt-2 is excluded. The ability of L3T4 but not Lyt-2 to participate in such a complex with class II-restricted T-cell antigen receptors may explain the striking correlation between class II restriction and L3T4 expression in the peripheral T-cell pool.
小鼠T细胞表面分子Lyt-2和L3T4在抗原特异性T细胞的激活中发挥作用。目前关于这些分子功能的公认模型提出,Lyt-2和L3T4会增加T细胞抗原受体与抗原呈递细胞上与主要组织相容性复合体(MHC)分子相关的抗原之间相互作用的总体亲和力。我们使用了两个不寻常的Lyt-2⁺ L3T4⁺ II类MHC限制性T细胞克隆,来测试当T细胞抗原受体受II类MHC限制时,Lyt-2是否能替代L3T4。针对L3T4的单克隆抗体显著抑制了两个T细胞克隆的抗原诱导的淋巴因子产生。抗Lyt-2单克隆抗体则没有作用。这些结果强烈表明,在抗原识别过程中,L3T4与II类限制性T细胞抗原受体在物理上紧密相连,可能是作为一个排除了Lyt-2的多分子复合物的一部分。L3T4而非Lyt-2能够与II类限制性T细胞抗原受体形成这样一个复合物,这可能解释了在外周T细胞库中II类限制与L3T4表达之间的显著相关性。