Malek T R, Chan C, Glimcher L H, Germain R N, Shevach E M
J Immunol. 1985 Sep;135(3):1826-33.
We have assessed the inhibitory effects of various monoclonal antibodies on the expression of the IL 2 receptor. Anti-LFA-1, but not anti-Ly-2, markedly inhibited the induction of the IL 2 receptor on the Ly-2+ subset. T-depleted spleen cells, L cells, and B lymphoma cells all functioned as potent accessory cells (AC) for the induction of the IL 2 receptor on L3T4+ T cells. Anti-LFA-1 inhibited the induction of the IL 2 receptor irrespective of the type of AC used. Anti-L3T4 only inhibited the induction of IL 2 receptor expression when L cells were the source of AC. The inhibitory capacity of anti-L3T4 was not related to the expression of Ia on the AC population, because the magnitude of inhibition was comparable in cultures containing either Ia+ or Ia- L cells, whereas no inhibition was seen with either Ia+ or Ia-B lymphoma cells. We conclude from these studies that LFA-1 plays a critical role in mitogen-induced activation of both T cell subsets by promoting both T-AC and T-T interactions. Although anti-L3T4 can inhibit T cell activation in the absence of the recognition of Ia, the mechanism of inhibition and the proposed target molecule for L3T4 on the AC or the T cell have not been determined in our studies. A number of different models for the function of this cell surface antigen are discussed.
我们评估了各种单克隆抗体对白细胞介素2(IL-2)受体表达的抑制作用。抗淋巴细胞功能相关抗原1(anti-LFA-1),而非抗Ly-2,显著抑制了Ly-2⁺亚群上IL-2受体的诱导。去除T细胞的脾细胞、L细胞和B淋巴瘤细胞均可作为L3T4⁺T细胞上IL-2受体诱导的有效辅助细胞(AC)。无论使用何种类型的AC,anti-LFA-1均能抑制IL-2受体的诱导。仅当L细胞作为AC来源时,抗L3T4才抑制IL-2受体表达的诱导。抗L3T4的抑制能力与AC群体上Ia的表达无关,因为在含有Ia⁺或Ia⁻L细胞的培养物中抑制程度相当,而Ia⁺或Ia⁻B淋巴瘤细胞均未观察到抑制作用。我们从这些研究中得出结论,LFA-1通过促进T-AC和T-T相互作用,在丝裂原诱导的两个T细胞亚群的激活中起关键作用。尽管在未识别Ia的情况下抗L3T4可抑制T细胞激活,但在我们的研究中尚未确定抑制机制以及L3T4在AC或T细胞上的假定靶分子。本文讨论了该细胞表面抗原功能的多种不同模型。