Loke P'ng, Allison James P
Howard Hughes Medical Institute, University of California, Berkeley, Berkeley, CA, USA.
Arthritis Res Ther. 2004;6(5):208-14. doi: 10.1186/ar1225. Epub 2004 Aug 5.
Whereas B7-1/B7-2 and CD28/cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) serve as the main switches regulating the clonal composition of activated naive T cells, other B7 family members fine-tune the expansion and properties of activated T cells. Inducible costimulatory molecule (ICOS)-B7h promotes T-dependent antibody isotype switching and expansion of effector cells. Effector T cells trafficking into inflamed tissues interact with antigen-presenting cells there and are regulated by PD-1 and its ligands. B7-H3 and B7x could control the interaction between effector T cells and the peripheral tissues. The different varieties of regulatory T cells could regulate both naive T cell activation and effector function through costimulatory receptor/ligands.
虽然B7-1/B7-2和CD28/细胞毒性T淋巴细胞相关抗原4(CTLA-4)作为调节活化幼稚T细胞克隆组成的主要开关,但其他B7家族成员可微调活化T细胞的扩增和特性。诱导性共刺激分子(ICOS)-B7h促进T细胞依赖性抗体亚型转换和效应细胞扩增。迁移至炎症组织的效应T细胞与那里的抗原呈递细胞相互作用,并受程序性死亡受体1(PD-1)及其配体调节。B7-H3和B7x可控制效应T细胞与外周组织之间的相互作用。不同种类的调节性T细胞可通过共刺激受体/配体调节幼稚T细胞活化和效应功能。