Saito S, Imanishi K, Araake M, Yan X J, Igarashi H, Uchiyama T
Department of Microbiology, Tokyo Women's Medical College.
Microbiol Immunol. 1991;35(8):661-73. doi: 10.1111/j.1348-0421.1991.tb01598.x.
Relative ability of distinct isotypes of human major histocompatibility complex class II molecules to bind staphylococcal enterotoxin A (SEA) was investigated. SEA-binding was observed in L cells transfected with DR2 and DQw1 genes. By contrast, it was not detected in L cells transfected with DPw4 and DP (Cp63) genes. All the transfectants supported SEA-induced IL-2 production by human T cells. Levels of the accessory activity were low in the DPw4 and DP (Cp63) transfectants compared with the DR2 and DQw1 transfectants. In view of the observation that all the transfectants express well the transfected gene products on their surface, the results indicate that DR and DQ molecules bind SEA with high affinity, while DP molecules bind it with fairly low affinity.
研究了人类主要组织相容性复合体II类分子不同同种型结合葡萄球菌肠毒素A(SEA)的相对能力。在用DR2和DQw1基因转染的L细胞中观察到SEA结合。相比之下,在用DPw4和DP(Cp63)基因转染的L细胞中未检测到。所有转染细胞均支持SEA诱导的人T细胞产生IL-2。与DR2和DQw1转染细胞相比,DPw4和DP(Cp63)转染细胞的辅助活性水平较低。鉴于观察到所有转染细胞均在其表面良好表达转染的基因产物,结果表明DR和DQ分子以高亲和力结合SEA,而DP分子以相当低的亲和力结合SEA。