Tsuji Masayuki, Komatsu Noriko, Kawamoto Shimpei, Suzuki Keiichiro, Kanagawa Osami, Honjo Tasuku, Hori Shohei, Fagarasan Sidonia
Laboratory for Mucosal Immunity, RIKEN, Yokohama 1-7-22, Tsurumi, Yokohama, 230-0045, Japan.
Science. 2009 Mar 13;323(5920):1488-92. doi: 10.1126/science.1169152.
Most of the immunoglobulin A (IgA) in the gut is generated by B cells in the germinal centers of Peyer's patches through a process that requires the presence of CD4+ follicular B helper T(TFH) cells. The nature of these T(FH) cells in Peyer's patches has been elusive. Here, we demonstrate that suppressive Foxp3+CD4+ T cells can differentiate into TFH cells in mouse Peyer's patches. The conversion of Foxp3+ T cells into TFH cells requires the loss of Foxp3 expression and subsequent interaction with B cells. Thus, environmental cues present in gut Peyer's patches promote the selective differentiation of distinct helper T cell subsets, such as TFH cells.
肠道中的大多数免疫球蛋白A(IgA)是由派尔集合淋巴结生发中心的B细胞通过一个需要CD4 +滤泡辅助性T(TFH)细胞存在的过程产生的。这些派尔集合淋巴结中的TFH细胞的性质一直难以捉摸。在这里,我们证明了抑制性Foxp3 + CD4 + T细胞可以在小鼠派尔集合淋巴结中分化为TFH细胞。Foxp3 + T细胞向TFH细胞的转化需要Foxp3表达的丧失以及随后与B细胞的相互作用。因此,肠道派尔集合淋巴结中存在的环境信号促进了不同辅助性T细胞亚群(如TFH细胞)的选择性分化。