Department of Molecular & Cellular Biology, Centro Nacional de Biotecnología; Consejo Superior de Investigaciones Científicas (CNB-CSIC), Darwin 3, 28049, Madrid, Spain.
Hospital de Santa Cristina, Instituto de Investigación Sanitaria Princesa, 28009, Madrid, Spain.
Nat Commun. 2017 Nov 17;8(1):1591. doi: 10.1038/s41467-017-01661-7.
Bacterial phagocytosis and antigen cross-presentation to activate CD8 T cells are principal functions of professional antigen presenting cells. However, conventional CD4 T cells also capture and kill bacteria from infected dendritic cells in a process termed transphagocytosis (also known as transinfection). Here, we show that transphagocytic T cells present bacterial antigens to naive CD8 T cells, which proliferate and become cytotoxic in response. CD4 T-cell-mediated antigen presentation also occurs in vivo in the course of infection, and induces the generation of central memory CD8 T cells with low PD-1 expression. Moreover, transphagocytic CD4 T cells induce protective anti-tumour immune responses by priming CD8 T cells, highlighting the potential of CD4 T cells as a tool for cancer immunotherapy.
细菌吞噬作用和抗原交叉呈递以激活 CD8 T 细胞是专业抗原呈递细胞的主要功能。然而,传统的 CD4 T 细胞也可以在称为吞噬作用(也称为转染)的过程中从感染的树突状细胞中捕获和杀死细菌。在这里,我们表明吞噬性 T 细胞将细菌抗原呈递给幼稚的 CD8 T 细胞,后者增殖并产生应答的细胞毒性。CD4 T 细胞介导的抗原呈递也在感染过程中发生在体内,并诱导具有低 PD-1 表达的中央记忆 CD8 T 细胞的产生。此外,吞噬性 CD4 T 细胞通过激活 CD8 T 细胞来诱导抗肿瘤免疫应答,突出了 CD4 T 细胞作为癌症免疫疗法工具的潜力。