Herrmann T, Accolla R S, MacDonald H R
Ludwig Institute for Cancer Research, Epalinges, Switzerland.
Eur J Immunol. 1989 Nov;19(11):2171-4. doi: 10.1002/eji.1830191131.
The stimulation of T cells by staphylococcal enterotoxins (SE) is strictly dependent on major histocompatibility complex (MHC) class II-bearing cells. The interaction between SE and MHC class II molecules was studied on the human B cell lymphoma Raji and its MHC class II-negative variant RJ 2.2.5. Affinity purification with SEA and SEB matrix allowed the isolation of HLA-DR-like molecules from detergent lysates of 125I surface-labeled Raji cells, but not from RJ 2.2.5 cells. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis also revealed preferences in the binding of other SE such as SED, SEE and toxic shock syndrome toxin 1 to DR-like molecules, SEC2 to HLA-DQ-like molecules and SEC3 to DR- and DQ-like molecules. Preadsorption of the different MHC class II MHC isotypes confirmed the preferential binding of SEA to DR and of SEC2 to DQ. The implications of these findings for the understanding of SE-induced T cell activation and the potency of SE as a tool in the study of MHC class II antigens are discussed.
葡萄球菌肠毒素(SE)对T细胞的刺激严格依赖于携带主要组织相容性复合体(MHC)II类分子的细胞。在人B细胞淋巴瘤Raji及其MHC II类阴性变体RJ 2.2.5上研究了SE与MHC II类分子之间的相互作用。用SEA和SEB基质进行亲和纯化,能够从125I表面标记的Raji细胞的去污剂裂解物中分离出HLA-DR样分子,但不能从RJ 2.2.5细胞中分离出来。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳还揭示了其他SE,如SED、SEE和中毒性休克综合征毒素1与DR样分子的结合偏好,SEC2与HLA-DQ样分子的结合偏好,以及SEC3与DR和DQ样分子的结合偏好。不同MHC II类同种型的预吸附证实了SEA对DR的优先结合以及SEC2对DQ的优先结合。讨论了这些发现对于理解SE诱导的T细胞活化以及SE作为研究MHC II类抗原工具的效力的意义。