Takahashi K, Isobe T, Ohtsuki Y, Sonobe H, Yamaguchi H, Akagi T
Am J Clin Pathol. 1985 Jan;83(1):69-72. doi: 10.1093/ajcp/83.1.69.
S-100 protein was detected in a small number of human peripheral T-lymphocytes by a direct immunoperoxidase method with the use of monospecific antibody to S-100 protein. Complemented-mediated lysis using monoclonal antibodies revealed that the S-100+ T-lymphocytes bore OKT3, OKT8, and OKT11 antigens but not OKT4, OKM1, HLA-DR, HNK1 (Leu-7) antigens on their surface. Immunoelectron micrography showed that S-100 T-lymphocytes were small lymphocytes with poorly developed cellular organelles. These findings clearly indicated that S-100+ T-lymphocytes belonged to the OKT8+ T-cell subset, the so-called suppressor/cytotoxic T-cell subset. Although the function of the S-100+ T-lymphocytes is unclear, S-100 protein may be a useful cytoplasmic marker for the subdivision of the heterogeneous OKT8+ lymphocyte population.
采用针对S-100蛋白的单特异性抗体,通过直接免疫过氧化物酶法在少数人外周血T淋巴细胞中检测到了S-100蛋白。使用单克隆抗体进行补体介导的细胞溶解显示,S-100阳性T淋巴细胞表面带有OKT3、OKT8和OKT11抗原,但不带有OKT4、OKM1、HLA-DR、HNK1(Leu-7)抗原。免疫电子显微镜检查显示,S-100阳性T淋巴细胞是细胞器发育不良的小淋巴细胞。这些发现清楚地表明,S-100阳性T淋巴细胞属于OKT8阳性T细胞亚群,即所谓的抑制/细胞毒性T细胞亚群。尽管S-100阳性T淋巴细胞的功能尚不清楚,但S-100蛋白可能是用于区分异质性OKT8阳性淋巴细胞群体的一种有用的细胞质标志物。