Institut National de la Santé et de la Recherche Médicale, Unité 891, Centre de Recherche en Cancérologie de Marseille, F-13009, Marseille, France.
Mol Immunol. 2011 Sep;48(15-16):2214-9. doi: 10.1016/j.molimm.2011.06.436. Epub 2011 Jul 12.
T-cell activation and proliferation are regulated by cosignaling adhesion molecules involved in positive or negative signals. Programmed death (PD)-1 is one of immune inhibitory molecules that is expressed in activated T cells and is a promising target for immunotherapy. Both PD-1 ligands, PD-L1 and PD-L2 are expressed on antigen presenting cells (APCs) involved in the dialogue between a T cell and an APC. Here, we analysed the expression of these ligands, especially for PD-L2, on T cells. PD-L2 appears to be expressed on activated CD4 and CD8T cell subsets. Moreover, as PD-1 molecule, PD-L2 engagement at the surface of T cells is able to down-modulate cytokine production and cell proliferation. These observations indicate that PD-L2 is expressed following activation and is involved in the regulation of T cell function, highlighting the level of complexity in the T cell cosignaling network.
T 细胞的激活和增殖受到参与正或负信号的共刺激粘附分子的调节。程序性死亡 (PD)-1 是一种免疫抑制分子,在激活的 T 细胞中表达,是免疫治疗的一个有前途的靶点。PD-1 的两个配体,PD-L1 和 PD-L2,都在参与 T 细胞与 APC 之间对话的抗原呈递细胞 (APC) 上表达。在这里,我们分析了这些配体的表达,特别是 PD-L2 的表达,在 T 细胞上。PD-L2 似乎在激活的 CD4 和 CD8T 细胞亚群上表达。此外,作为 PD-1 分子,PD-L2 在 T 细胞表面的结合能够下调细胞因子的产生和细胞增殖。这些观察结果表明,PD-L2 在激活后表达,并参与 T 细胞功能的调节,突出了 T 细胞共刺激信号网络的复杂程度。