T细胞受体
单克隆抗体
CD3型
克隆(Java方法)
分子生物学
表位
T细胞
生物
抗原
白细胞介素2
抗体
T淋巴细胞
受体
化学
细胞生物学
生物化学
免疫学
免疫系统
CD8型
基因
作者
Hans Yssel,Jean‐Pierre Aubry,R de Waal Malefijt,J E de Vries,Hergen Spits
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:1987-11-01
卷期号:139 (9): 2850-2855
被引量:24
标识
DOI:10.4049/jimmunol.139.9.2850
摘要
In this study the effect of anti-cluster designation (CD) 2 monoclonal antibodies (mAb) on the activation of a cloned human T cell line, HY837, after triggering the CD3/T cell receptor (TcR) complex by anti-CD3 or anti-TcR mAb is described. HY837, which reacts with a series of mAb directed at different epitopes on the TcR, could be induced to proliferation and interleukin 2 (IL-2) production by soluble mAb directed at the CD3/TcR complex in the absence of accessory cells. mAb directed at the CD2 epitope T11-1 were shown to block the IL-2 production by HY837, as well as the expression of the IL-2 receptor, induced by anti-CD3 mAb, resulting in the inhibition of the proliferative response. The effect of anti-CD2 mAb on the proliferative response of HY837, induced by anti-CD3 mAb, was not due to a competition for Fc binding sites. In contrast, the proliferative responses and IL-2 production of HY837, induced by mAb directed at the TcR, were shown to be enhanced by the action of the anti-CD2 mAb. These results indicate that effects mediated by anti-CD3/TcR mAb cannot always be extrapolated to antigen-mediated effects and show that anti-CD2 mAb may regulate the T cell response, induced by mAb directed at the CD3/TcR complex, depending on which part of this complex is triggered during activation.
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