超抗原
CD28
T细胞
生物
抗原提呈细胞
T细胞受体
细胞生物学
抗原
T淋巴细胞
免疫学
分子生物学
免疫系统
作者
Hiroshi Ohnishi,Toshiaki Tanaka,Jiro Takahara,Malak Kotb
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:1993-04-15
卷期号:150 (8): 3207-3214
被引量:17
标识
DOI:10.4049/jimmunol.150.8.3207
摘要
The CD28 pathway functions to provide costimulatory signals that are required for TCR-mediated activation of T cells. The role of this pathway in superantigenic stimulation of resting human T cells was investigated in the presence and absence of APC using a streptococcal superantigen, pep M5. Anti-B7/BB1 mAb inhibited the response of T cells when pep M5 was presented by APC. In the absence of APC, cross-linking CD28 by anti-CD28 mAb provides signals that synergize with APC-derived cytokines and with superantigen resulting in T cell proliferation. Anti-HLA-DR, -DQ mAb blocked the response of T cells to pep M5 presented by APC but had no effect on the response of purified T cells to the superantigen costimulated via CD28 cross-linking. These data show that the CD28 pathway is important for superantigenic stimulation of T cells and that signaling through this pathway can substitute for the APC-associated costimulatory activity that is essential for T cell stimulation. Moreover, the results are consistent with the notion that, in the presence of appropriate costimulation, pep M5 can directly interact with T cells and induce them to proliferate.
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