Department of Immunology, Blavatnik Institute, Harvard Medical School, and Evergrande Center for Immunologic Diseases, Harvard Medical School and Brigham and Women's Hospital, Boston, MA 02115, USA.
Department of Immunology, Blavatnik Institute, Harvard Medical School, and Evergrande Center for Immunologic Diseases, Harvard Medical School and Brigham and Women's Hospital, Boston, MA 02115, USA; Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Cell Rep. 2020 Jun 30;31(13):107827. doi: 10.1016/j.celrep.2020.107827.
The PD-1 pathway regulates dysfunctional T cells in chronic infection and cancer, but the role of this pathway during acute infection remains less clear. Here, we demonstrate that PD-1 signals are needed for optimal memory. Mice deficient in the PD-1 pathway exhibit impaired CD8 T cell memory following acute influenza infection, including reduced virus-specific CD8 T cell numbers and compromised recall responses. PD-1 blockade during priming leads to similar differences early post-infection but without the defect in memory formation, suggesting that timing and/or duration of PD-1 blockade could be tailored to modulate host responses. Our studies reveal a role for PD-1 as an integrator of CD8 T cell signals that promotes CD8 T cell memory formation and suggest PD-1 continues to fine-tune CD8 T cells after they migrate into non-lymphoid tissues. These findings have important implications for PD-1-based immunotherapy, in which PD-1 inhibition may influence memory responses in patients.
PD-1 通路调节慢性感染和癌症中功能失调的 T 细胞,但该通路在急性感染期间的作用尚不清楚。在这里,我们证明 PD-1 信号对于最佳记忆是必需的。在急性流感感染后,缺乏 PD-1 通路的小鼠表现出受损的 CD8 T 细胞记忆,包括病毒特异性 CD8 T 细胞数量减少和回忆反应受损。在启动时阻断 PD-1 会导致感染后早期出现类似的差异,但不会形成记忆缺陷,这表明 PD-1 阻断的时间和/或持续时间可以调整以调节宿主反应。我们的研究揭示了 PD-1 作为整合 CD8 T 细胞信号的作用,促进 CD8 T 细胞记忆形成,并表明 PD-1 在 CD8 T 细胞迁移到非淋巴组织后继续微调 CD8 T 细胞。这些发现对基于 PD-1 的免疫疗法具有重要意义,其中 PD-1 抑制可能影响患者的记忆反应。