Lancki D W, Prystowsky M B, Vogel S N, Beller D I, Dialynas D P, Fitch F W
J Immunol. 1984 Oct;133(4):2051-7.
Monoclonal antibodies recognizing murine T lymphocyte cell surface structures implicated in T lymphocyte-mediated cytolysis, including Lyt-2, L3T4, LFA-1, and a cytolytic T lymphocyte (CTL) clonotypic determinant, were used as probes to investigate the role of these structures in lymphokine production by T cell clones induced by antigen or lectin. The clone-specific antibody 384.5 bound to and inhibited antigen-induced lymphokine production by the L3 CTL clone, but did not affect lymphokine production by other T cell clones. Antibodies against the T cell surface structures Lyt-2 or L3T4, which are expressed by mutually exclusive T cell subsets, inhibited antigen-induced lymphokine production by class I major histocompatibility complex (MHC) antigen-reactive CTL clones or an M1s-reactive helper T lymphocyte (HTL) clone, respectively. Antibody against the broadly distributed LFA-1 molecule inhibited antigen-induced lymphokine production by all of the clones tested. Lectin-induced lymphokine production by cloned T cells was not inhibited by the clonotypic antibody, anti-Lyt-2, or anti-LFA-1; slight inhibition of the HTL clone was observed with the anti-L3T4 antibody. None of these structures appear to be uniquely involved with a particular functional response. Our results suggest that each of these structures is involved with the interactions between the effector cell and the stimulating cell leading to lymphokine production.
识别与T淋巴细胞介导的细胞溶解相关的小鼠T淋巴细胞细胞表面结构的单克隆抗体,包括Lyt-2、L3T4、淋巴细胞功能相关抗原-1(LFA-1)和一种细胞毒性T淋巴细胞(CTL)克隆型决定簇,被用作探针来研究这些结构在由抗原或凝集素诱导的T细胞克隆产生淋巴因子中的作用。克隆特异性抗体384.5与L3 CTL克隆结合并抑制抗原诱导的淋巴因子产生,但不影响其他T细胞克隆产生淋巴因子。针对由相互排斥的T细胞亚群表达的T细胞表面结构Lyt-2或L3T4的抗体,分别抑制了I类主要组织相容性复合体(MHC)抗原反应性CTL克隆或M1s反应性辅助性T淋巴细胞(HTL)克隆的抗原诱导的淋巴因子产生。针对广泛分布的LFA-1分子的抗体抑制了所有测试克隆的抗原诱导的淋巴因子产生。克隆的T细胞由凝集素诱导产生淋巴因子不受克隆型抗体、抗Lyt-2或抗LFA-1的抑制;抗L3T4抗体对HTL克隆有轻微抑制作用。这些结构似乎都不是唯一参与特定功能反应的。我们的结果表明,这些结构中的每一个都参与了效应细胞与刺激细胞之间导致淋巴因子产生的相互作用。