Shin Changsik, Han Jae-A, Koh Hyein, Choi Bongseo, Cho Yongbin, Jeong Hyeongmin, Ra Jea-Sun, Sung Pil Soo, Shin Eui-Cheol, Ryu Seongho, Do Yoonkyung
School of Life Sciences, Ulsan National Institute of Science and Technology, UNIST-gil 50, Ulsan 689-798, Republic of Korea.
Laboratory of Cellular Physiology and Immunology and Chris Browne Center, The Rockefeller University, New York, NY 10065, USA.
Cell Rep. 2015 Jun 30;11(12):1929-40. doi: 10.1016/j.celrep.2015.05.042. Epub 2015 Jun 18.
Recent studies on T follicular helper (Tfh) cells have significantly advanced our understanding of T cell-dependent B cell responses. However, little is known about the early stage of Tfh cell commitment by dendritic cells (DCs), particularly by the conventional CD8α(+) and CD8α(-) DC subsets. We show that CD8α(-) DCs localized at the interfollicular zone play a pivotal role in the induction of antigen-specific Tfh cells by upregulating the expression of Icosl and Ox40l through the non-canonical NF-κB signaling pathway. Tfh cells induced by CD8α(-) DCs function as true B cell helpers, resulting in significantly increased humoral immune responses against various human pathogenic antigens, including Yersinia pestis LcrV, HIV Gag, and hepatitis B surface antigen. Our findings uncover a mechanistic role of CD8α(-) DCs in the initiation of Tfh cell differentiation and thereby provide a rationale for investigating CD8α(-) DCs in enhancing antigen-specific humoral immune responses for improving vaccines and therapeutics.
近期关于滤泡辅助性T细胞(Tfh)的研究极大地推动了我们对T细胞依赖性B细胞应答的理解。然而,对于树突状细胞(DC),尤其是传统的CD8α(+)和CD8α(-) DC亚群在Tfh细胞定向分化早期阶段的作用却知之甚少。我们发现,位于滤泡间区的CD8α(-) DC通过非经典NF-κB信号通路上调Icosl和Ox40l的表达,在抗原特异性Tfh细胞的诱导中起关键作用。由CD8α(-) DC诱导的Tfh细胞作为真正的B细胞辅助细胞发挥作用,导致针对多种人类致病抗原,包括鼠疫耶尔森菌LcrV、HIV Gag和乙肝表面抗原的体液免疫应答显著增强。我们的研究结果揭示了CD8α(-) DC在Tfh细胞分化起始中的机制性作用,从而为研究CD8α(-) DC在增强抗原特异性体液免疫应答以改进疫苗和治疗方法方面提供了理论依据。