Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Nat Immunol. 2018 Mar;19(3):255-266. doi: 10.1038/s41590-018-0052-z. Epub 2018 Feb 23.
Key events in T cell-dependent antibody responses, including affinity maturation, are dependent on the B cell's presentation of antigen to helper T cells at critical checkpoints in germinal-center formation in secondary lymphoid organs. Here we found that signaling via Toll-like receptor 9 (TLR9) blocked the ability of antigen-specific B cells to capture, process and present antigen and to activate antigen-specific helper T cells in vitro. In a mouse model in vivo and in a human clinical trial, the TLR9 agonist CpG enhanced the magnitude of the antibody response to a protein vaccine but failed to promote affinity maturation. Thus, TLR9 signaling might enhance antibody titers at the expense of the ability of B cells to engage in germinal-center events that are highly dependent on B cells' capture and presentation of antigen.
T 细胞依赖性抗体反应中的关键事件,包括亲和力成熟,依赖于 B 细胞在次级淋巴器官生发中心形成的关键检查点向辅助性 T 细胞呈递抗原。在这里,我们发现 Toll 样受体 9(TLR9)的信号传导阻断了抗原特异性 B 细胞捕获、加工和呈递抗原以及在体外激活抗原特异性辅助性 T 细胞的能力。在体内的小鼠模型和人体临床试验中,TLR9 激动剂 CpG 增强了对蛋白质疫苗的抗体反应的幅度,但未能促进亲和力成熟。因此,TLR9 信号可能会以牺牲 B 细胞参与生发中心事件的能力为代价来提高抗体滴度,而这些事件高度依赖于 B 细胞对抗原的捕获和呈递。