Department of Immunology, University of Washington School of Medicine, Seattle, WA.
J Exp Med. 2020 Feb 3;217(2). doi: 10.1084/jem.20190849.
CD4+ T follicular helper (Tfh) cells dominate the acute response to a blood-stage Plasmodium infection and provide signals to direct B cell differentiation and protective antibody expression. We studied antigen-specific CD4+ Tfh cells responding to Plasmodium infection in order to understand the generation and maintenance of the Tfh response. We discovered that a dominant, phenotypically stable, CXCR5+ Tfh population emerges within the first 4 d of infection and results in a CXCR5+ CCR7+ Tfh/central memory T cell response that persists well after parasite clearance. We also found that CD4+ T cell priming by B cells was both necessary and sufficient to generate this Tfh-dominant response, whereas priming by conventional dendritic cells was dispensable. This study provides important insights into the development of CD4+ Tfh cells during Plasmodium infection and highlights the heterogeneity of antigen-presenting cells involved in CD4+ T cell priming.
CD4+ T 滤泡辅助(Tfh)细胞主导对疟原虫血期感染的急性反应,并提供信号以指导 B 细胞分化和保护性抗体表达。我们研究了针对疟原虫感染的抗原特异性 CD4+ Tfh 细胞,以了解 Tfh 反应的产生和维持。我们发现,在感染后的前 4 天内,出现了一种占主导地位、表型稳定的 CXCR5+ Tfh 细胞群,导致 CXCR5+ CCR7+ Tfh/中央记忆 T 细胞反应在寄生虫清除后仍能持续存在。我们还发现,B 细胞对 CD4+T 细胞的初始作用是产生这种 Tfh 优势反应所必需和充分的,而传统树突状细胞的初始作用则是可有可无的。这项研究为疟原虫感染期间 CD4+Tfh 细胞的发展提供了重要的见解,并强调了参与 CD4+T 细胞初始作用的抗原呈递细胞的异质性。