Department of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark.
Department of Clinical Immunology, Aarhus University Hospital, 8200 Aarhus N, Denmark.
Immunol Lett. 2018 Aug;200:26-32. doi: 10.1016/j.imlet.2018.06.003. Epub 2018 Jun 11.
Similar to CD4 T cells, precursor CD8 T cells are thought to depend on a co-stimulatory signal through CD28 for proliferation and differentiation into effector cells. CD46 is another co-stimulatory receptor that promotes differentiation of CD4 T-helper cells type 1 (Th1 cells) into a regulatory phenotype with a switch from IFN-γ towards IL-10-secretion over time. Whether CD46 exerts a similar function on CD8 T cells remains to be fully elucidated. Here, we demonstrate that CD46 co-stimulation induced secretion of IFN-γ as well as expansion of IFN-γ-secreting CD8 T cells. In contrast to CD46 co-stimulation of CD4 T cells, CD8 T cells did not differentiate into a regulatory IL-10-secreting phenotype. This demonstrates that CD46 is a co-stimulatory receptor on CD8 T cells, and that it exerts separate functions during CD4 and CD8 T-cell differentiation.
类似于 CD4 T 细胞,前体 CD8 T 细胞被认为依赖于通过 CD28 的共刺激信号来增殖和分化为效应细胞。CD46 是另一种共刺激受体,可促进 CD4 T 辅助细胞 1 型(Th1 细胞)向调节表型分化,随着时间的推移,从 IFN-γ 向 IL-10 分泌转变。CD46 是否对 CD8 T 细胞具有类似的功能仍有待充分阐明。在这里,我们证明 CD46 的共刺激诱导了 IFN-γ 的分泌以及 IFN-γ 分泌的 CD8 T 细胞的扩增。与 CD4 T 细胞的 CD46 共刺激相反,CD8 T 细胞不会分化为具有调节性 IL-10 分泌表型的细胞。这表明 CD46 是 CD8 T 细胞上的共刺激受体,并且在 CD4 和 CD8 T 细胞分化过程中发挥不同的功能。