Jacquot S, Kobata T, Iwata S, Schlossman S F, Morimoto C
Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Cell Immunol. 1997 Jul 10;179(1):48-54. doi: 10.1006/cimm.1997.1150.
CD27, a tumor necrosis factor receptor family member, is a constimulatory molecule for T and B cell activation. We demonstrate here that CD27 signaling is critical for T cell activation in the autologous mixed lymphocyte reaction (aMLR) and for aMLR-induced generation of regulatory T cells that suppress pokeweed mitogen-driven immunoglobulin G synthesis by B cells. Moreover, CD27, expressed on CD45RA+ CD4+ T cells, is directly involved in the suppressor function of aMLR-activated CD4+ T cells, probably by interfering with the interaction between CD70, the CD27 ligand, expressed on CD45RO+ CD4+ helper T cells, and CD27, expressed on B cells. CD8+ T cells, which are required in this system to obtain suppression, on the other hand, do not need CD27 engagement to exert their suppressor function.
CD27是肿瘤坏死因子受体家族成员,是T细胞和B细胞激活的共刺激分子。我们在此证明,CD27信号对于自体混合淋巴细胞反应(aMLR)中的T细胞激活以及aMLR诱导的调节性T细胞生成至关重要,这些调节性T细胞可抑制B细胞受商陆丝裂原驱动的免疫球蛋白G合成。此外,表达于CD45RA+ CD4+ T细胞上的CD27直接参与aMLR激活的CD4+ T细胞的抑制功能,可能是通过干扰表达于CD45RO+ CD4+辅助性T细胞上的CD27配体CD70与表达于B细胞上的CD27之间的相互作用。另一方面,该系统中实现抑制作用所需的CD8+ T细胞,发挥其抑制功能不需要CD27参与。