CD28
T细胞受体
CD8型
生物
T细胞
细胞生物学
细胞毒性T细胞
细胞因子
CD3型
分子生物学
免疫学
免疫系统
体外
生物化学
作者
Jane A. Gross,Eleni Callas,James P. Allison
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:1992-07-15
卷期号:149 (2): 380-388
被引量:316
标识
DOI:10.4049/jimmunol.149.2.380
摘要
T cell activation requires Ag-specific stimulation mediated by the TCR as well as an additional stimulus provided by Ag presenting cells. On human T cells, it has been shown that antibodies to the Ag CD28 can provide a potent amplification signal for cytokine production and proliferation. Here we describe the production of a mAb to the murine homologue of CD28, and the use of this antibody to examine the function and distribution of CD28 in the mouse. Anti-murine CD28 synergizes with TCR-mediated signals to greatly enhance lymphokine production and proliferation of T cells, and the CD28 signal is not blocked by cyclosporin A. In the peripheral lymphoid organs and in the blood of the mouse, all CD4+ and CD8+ T cells express CD28. In the thymus, CD28 expression is highest on immature CD3-, CD8+ and CD4+8+ cells, and on CD4-8- cells that express alpha beta and tau delta TCR. The level of CD28 on mature CD4+ and CD8+ alpha beta TCR+ thymocytes is two- to fourfold lower than on the immature cells. The potent costimulatory function of CD28 on mature T cells, together with the high level of expression on CD4+8+ thymocytes, suggest that this costimulatory receptor might play an important role in T cell development and activation.
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