Wesselborg S, Janssen O, Pechhold K, Kabelitz D
Institut für Immunologie, Universität Heidelberg, Federal Republic of Germany.
J Exp Med. 1991 Feb 1;173(2):297-304. doi: 10.1084/jem.173.2.297.
The CD2 antigen is the target for an "alternative" T cell activation pathway. Numerous studies have demonstrated that pairs of monoclonal antibodies (mAbs) directed toward two different epitopes are required for activation of T cell receptor (TCR)-alpha/beta + T cells via CD2. We have now explored the activation of human TCR-gamma/delta + T cell clones by a panel of anti-CD2 mAbs directed against the sheep erythrocyte-binding (T11.1) epitope of CD2. Seven of seven gamma/delta + clones expressing different molecular forms of the TCR-gamma/delta responded to stimulation by a single anti-CD2 mAb (OKT11, 9E8, BW0110, M-T910) with IL-2 secretion and/or proliferation. Immobilization of anti-CD2 mAbs in microculture plates was essential for activation of gamma/delta + clones, which occurred in the absence of feeder cells. In addition to interleukin 2 (IL-2) production and proliferation, anti-CD2 mAbs also triggered cytotoxic effector activity in gamma/delta + clones as measured against FcR+ P815 target cells. In contrast to gamma/delta + clones (but in line with established data), none of five CD4+ or CD8+ TCR-alpha/beta + clones were activated by any of the tested individual anti-CD2 mAbs. Taken together, our results reveal a striking difference between cloned gamma/delta + and alpha/beta + T cells in that gamma/delta + T cells are selectively activated by a single anti-CD2 (T11.1) mAb, without need for the simultaneous signal of a second anti-CD2 mAb directed against another (T11.2 or T11.3) CD2 epitope.
CD2抗原是“替代性”T细胞激活途径的靶点。大量研究表明,通过CD2激活T细胞受体(TCR)α/β + T细胞需要针对两个不同表位的一对单克隆抗体(mAb)。我们现在研究了一组针对CD2的绵羊红细胞结合(T11.1)表位的抗CD2 mAb对人TCRγ/δ + T细胞克隆的激活作用。七个表达不同分子形式TCRγ/δ的γ/δ +克隆中有七个通过分泌白细胞介素-2(IL-2)和/或增殖对单一抗CD2 mAb(OKT11、9E8、BW0110、M-T910)的刺激产生反应。将抗CD2 mAb固定在微孔培养板中对于γ/δ +克隆的激活至关重要,这种激活在没有饲养细胞的情况下即可发生。除了产生IL-2和增殖外,抗CD2 mAb还触发了γ/δ +克隆对FcR + P815靶细胞的细胞毒性效应活性。与γ/δ +克隆不同(但与已有的数据一致),五个CD4 +或CD8 + TCRα/β +克隆中没有一个被任何测试的单个抗CD2 mAb激活。综上所述,我们的结果揭示了克隆的γ/δ +和α/β + T细胞之间的显著差异,即γ/δ + T细胞可被单一抗CD2(T11.1)mAb选择性激活,而无需针对另一个(T11.2或T11.3)CD2表位的第二个抗CD2 mAb的同时信号。