Yssel H, Aubry J P, de Waal Malefijt R, de Vries J E, Spits H
UNICET, Laboratories for Immunological Research, Dardilly, France.
J Immunol. 1987 Nov 1;139(9):2850-5.
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.
本研究描述了抗集群指定(CD)2单克隆抗体(mAb)对克隆的人T细胞系HY837活化的影响,该细胞系在用抗CD3或抗T细胞受体(TcR)单克隆抗体触发CD3/T细胞受体(TcR)复合物之后。HY837可与一系列针对TcR上不同表位的单克隆抗体发生反应,在无辅助细胞的情况下,可被针对CD3/TcR复合物的可溶性单克隆抗体诱导增殖并产生白细胞介素2(IL-2)。已证明,针对CD2表位T11-1的单克隆抗体可阻断HY837产生IL-2以及抗CD3单克隆抗体诱导的IL-2受体表达,从而抑制增殖反应。抗CD2单克隆抗体对抗CD3单克隆抗体诱导的HY837增殖反应的影响并非由于对Fc结合位点的竞争。相反,已证明抗CD2单克隆抗体的作用可增强针对TcR的单克隆抗体诱导的HY837增殖反应和IL-2产生。这些结果表明,抗CD3/TcR单克隆抗体介导的效应不能总是外推至抗原介导的效应,并且表明抗CD2单克隆抗体可能根据激活过程中该复合物的哪一部分被触发来调节由针对CD3/TcR复合物的单克隆抗体诱导的T细胞反应。