Engleman E G, Benike C J, Glickman E, Evans R L
J Exp Med. 1981 Jul 1;154(1):193-8. doi: 10.1084/jem.154.1.193.
Two major subsets of human T lymphocytes that are functionally analogous to the mouse Lyt-2+ and Lyt-2- subsets have been defined by their expression of two thymus-dependent membrane antigens, Leu-2 and Leu-3. Leu-2+,3- cells have suppressor/cytotoxic functions and Leu-2-,3+ cells have helper functions. These studies were designed to determine the effects of adding IgG1 monoclonal anti-Leu-2 and anti-Leu-3 antibodies to the mixed leukocyte reaction (MLR). At high concentrations, each antibody partially inhibited the proliferative response of unseparated T cells and abolished the response of the isolated subset having the appropriate phenotype. An IgG1 monoclonal antibody to HLA-A2 and an IgG2a antibody to Leu-1, a pan-T antigen, failed to inhibited the MLR. These results suggest that the Leu-2 and Leu-3 antigens may have a direct role in the mechanism whereby T cells recognize and respond to alloantigen.
通过两种胸腺依赖性膜抗原Leu-2和Leu-3的表达,已确定了人类T淋巴细胞的两个主要亚群,它们在功能上类似于小鼠的Lyt-2 +和Lyt-2-亚群。Leu-2 +,3-细胞具有抑制/细胞毒性功能,而Leu-2-,3 +细胞具有辅助功能。这些研究旨在确定向混合淋巴细胞反应(MLR)中添加IgG1单克隆抗Leu-2和抗Leu-3抗体的效果。在高浓度下,每种抗体部分抑制未分离T细胞的增殖反应,并消除具有适当表型的分离亚群的反应。针对HLA-A2的IgG1单克隆抗体和针对泛T抗原Leu-1的IgG2a抗体未能抑制MLR。这些结果表明,Leu-2和Leu-3抗原可能在T细胞识别和响应同种异体抗原的机制中起直接作用。