Tomai M A, Schlievert P M, Kotb M
Veteran's Administration Medical Center, Memphis, Tennessee 38104.
Infect Immun. 1992 Feb;60(2):701-5. doi: 10.1128/iai.60.2.701-705.1992.
A number of streptococcal products, including the streptococcal pyrogenic exotoxin (SPE) types A, B, and C as well as a 22-kDa fragment of M type 5 protein (pep M5), are potent stimulants of human T-lymphocyte blastogenesis and belong to the newly designated family of superantigens. The V beta usage of human T cells stimulated with these toxins was investigated by using the polymerase chain reaction. We demonstrate that SPE A, B, and C as well as pep M5 stimulate the proliferation of T cells in a dose-dependent manner. pep M5 stimulates cells bearing V beta 2, 4, and 8 elements of the T-cell receptor (TCR), whereas SPE A stimulates TCR V beta 2-, 12-, 14-, and 15-bearing cells. SPE B stimulated only cells expressing TCR V beta 8 elements, while SPE C stimulated cells expressing V beta 1, 2, 5.1, and 10. These studies reveal that the preferential usage of particular V beta elements is distinct for these different superantigens, which may be important in the pathogenesis of various streptococcal diseases.
多种链球菌产物,包括A、B和C型链球菌致热外毒素(SPE)以及M5型蛋白的22 kDa片段(pep M5),都是人类T淋巴细胞增殖的强效刺激剂,属于新指定的超抗原家族。通过聚合酶链反应研究了用这些毒素刺激的人类T细胞的Vβ使用情况。我们证明,SPE A、B和C以及pep M5以剂量依赖的方式刺激T细胞增殖。pep M5刺激带有T细胞受体(TCR)Vβ2、4和8元件的细胞,而SPE A刺激带有TCR Vβ2、12、14和15的细胞。SPE B仅刺激表达TCR Vβ8元件的细胞,而SPE C刺激表达Vβ1、2、5.1和10的细胞。这些研究表明,这些不同的超抗原对特定Vβ元件的优先使用情况不同,这可能在各种链球菌疾病的发病机制中具有重要意义。