Shin Changsik, Han Jae-A, Choi Bongseo, Cho Yoon-Kyoung, Do Yoonkyung, Ryu Seongho
School of Life Sciences, Ulsan National Institute of Science and Technology, UNIST-gil 50, Ulsan 44919, Republic of Korea.
School of Life Sciences, Ulsan National Institute of Science and Technology, UNIST-gil 50, Ulsan 44919, Republic of Korea; Center for Soft and Living Matter, Institute for Basic Science (IBS), UNIST-gil 50, Ulsan 44919, Republic of Korea.
Immunol Lett. 2016 Apr;172:21-8. doi: 10.1016/j.imlet.2016.01.009. Epub 2016 Feb 2.
T follicular helper (Tfh) cells, a true B cell helper, have a critical role in enhancing humoral immune responses. However, the initial differentiation of Tfh cells by dendritic cells (DCs), the most potent antigen presenting cells, has not been clearly understood, particularly in the knowledge of the two major conventional dendritic cell subsets, CD8α(+) DCs or CD8α(-) DCs. Here we demonstrated that the localization of CD8α(-) DCs in the marginal zone (MZ) bridging channels is closely associated with the induction of CXCR5(+)CCR7(low) Tfh cells. We also showed that the major source of IL-6 for inducing Tfh cells is provided from the activated CD4(+) T cells induced by CD8α(-) DCs, and IL-6 directly secreted from the DC subsets seems minor. CD8α(-) DCs were superior in inducing functional Tfh cells over other antigen presenting cells including B cells. We here observed the unknown intrinsic features of the DC subsets, suggesting the potential of utilizing the CD8α(-) DC subset as therapeutic vaccine for the regulation of humoral immune responses.
滤泡辅助性T(Tfh)细胞是真正的B细胞辅助细胞,在增强体液免疫反应中起关键作用。然而,树突状细胞(DCs)作为最强大的抗原呈递细胞,对Tfh细胞的初始分化作用尚未完全明确,尤其是在两种主要的传统树突状细胞亚群,即CD8α(+) DCs或CD8α(-) DCs方面。在此,我们证明了CD8α(-) DCs在边缘区(MZ)桥接通道中的定位与CXCR5(+)CCR7(low) Tfh细胞的诱导密切相关。我们还表明,诱导Tfh细胞的白细胞介素-6(IL-6)的主要来源是由CD8α(-) DCs诱导的活化CD4(+) T细胞,而DC亚群直接分泌的IL-6似乎作用较小。与包括B细胞在内的其他抗原呈递细胞相比,CD8α(-) DCs在诱导功能性Tfh细胞方面更具优势。我们在此观察到了DC亚群未知的内在特性,提示利用CD8α(-) DC亚群作为治疗性疫苗来调节体液免疫反应的潜力。