Second Division, Department of Internal Medicine, Hamamatsu University School of Medicine, Shizuoka, Japan.
Second Division, Department of Internal Medicine, Hamamatsu University School of Medicine, Shizuoka, Japan; Department of Laboratory Medicine, Hamamatsu University School of Medicine, Shizuoka, Japan.
Allergol Int. 2021 Jul;70(3):351-359. doi: 10.1016/j.alit.2021.01.008. Epub 2021 Mar 3.
Follicular helper T (Tfh) cells represent a unique subset of helper CD4 T cells in lymphoid follicles. Recently, Tfh cells were shown to play an important role in asthma through B cell differentiation. Conventional lung DCs are classified into two major subsets: conventional type 1 (cDC1) and type 2 (cDC2). Although the two subsets are different in driving particular T cell responses, the subset that induces Tfh cells in the asthmatic lung primarily has yet to be fully elucidated.
We evaluated Tfh cells, defined by the expression of CD4 and CXCR5, in HDM-challenged mice. Next, we characterized cDC1 and cDC2 purified from antigen-primed lung and examined their Tfh cell-inducing capacity. Additionally, the ability of lung DC-induced Tfh cells to cause germinal center B (GCB) cells to produce antigen-specific IgE was assessed.
In HDM-challenged mice, Bcl-6-expressing Tfh cells were significantly increased in the mediastinal lymph nodes. Lung cDC2, but not lung cDC1, increased after HDM priming, and cDC2 secreted larger amounts of IL-6 with higher ICOS-L expression than cDC1. In the co-cultures with OVA-specific naïve CD4 T cells, cDC2 from OVA-primed lung induced Bcl-6-expressing Tfh cells more efficiently, together with larger amounts of IL-6 and IL-21, than cDC1. Blockage of IL-6 or ICOS-L significantly reduced Tfh cell induction. Finally, cDC2-induced Tfh cells enabled GCB cells to produce OVA-specific IgE.
In asthmatic lung, cDC2 is the primary DC subset responsible for Tfh cell differentiation and plays an important role in humoral immunity in asthma by inducing Tfh cells.
滤泡辅助 T(Tfh)细胞是淋巴滤泡中辅助性 CD4 T 细胞的一个独特亚群。最近的研究表明,Tfh 细胞通过 B 细胞分化在哮喘中发挥重要作用。传统的肺部树突状细胞(DCs)可分为两个主要亚群:传统 1 型(cDC1)和 2 型(cDC2)。虽然这两个亚群在驱动特定的 T 细胞反应方面有所不同,但在哮喘肺部中诱导 Tfh 细胞的亚群尚未完全阐明。
我们评估了 HDM challenged 小鼠中 CD4 和 CXCR5 表达定义的 Tfh 细胞。接下来,我们从抗原致敏的肺部中分离纯化 cDC1 和 cDC2,并研究了它们诱导 Tfh 细胞的能力。此外,还评估了肺 DC 诱导的 Tfh 细胞促使生发中心 B(GCB)细胞产生抗原特异性 IgE 的能力。
在 HDM challenged 小鼠中,Bcl-6 表达的 Tfh 细胞在纵隔淋巴结中显著增加。在 HDM 致敏后,肺 cDC2 而非肺 cDC1 增加,cDC2 分泌的 IL-6 量更大,ICOS-L 表达更高。在与 OVA 特异性幼稚 CD4 T 细胞的共培养中,来自 OVA 致敏肺部的 cDC2 比 cDC1 更有效地诱导 Bcl-6 表达的 Tfh 细胞,同时分泌更多的 IL-6 和 IL-21。阻断 IL-6 或 ICOS-L 可显著减少 Tfh 细胞的诱导。最后,cDC2 诱导的 Tfh 细胞使 GCB 细胞能够产生 OVA 特异性 IgE。
在哮喘肺部中,cDC2 是负责 Tfh 细胞分化的主要 DC 亚群,通过诱导 Tfh 细胞在哮喘中的体液免疫中发挥重要作用。