Preferential Generation of Follicular B Helper T Cells from Foxp3 + T Cells in Gut Peyer's Patches

Author:

Tsuji Masayuki1234,Komatsu Noriko1234,Kawamoto Shimpei1234,Suzuki Keiichiro1234,Kanagawa Osami1234,Honjo Tasuku1234,Hori Shohei1234,Fagarasan Sidonia1234

Affiliation:

1. Laboratory for Mucosal Immunity, RIKEN, Yokohama 1-7-22, Tsurumi, Yokohama, 230-0045, Japan.

2. Research Unit for Immune Homeostasis, RIKEN, Yokohama 1-7-22, Tsurumi, Yokohama, 230-0045, Japan.

3. Laboratory for Autoimmune Regulation, Research Center for Allergy and Immunology, RIKEN, Yokohama 1-7-22, Tsurumi, Yokohama, 230-0045, Japan.

4. Department of Immunology and Genomic Medicine, Kyoto University, Graduate School of Medicine, Sakyo-ku, Kyoto 606-8501, Japan.

Abstract

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(T FH ) 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 T FH cells in mouse Peyer's patches. The conversion of Foxp3 + T cells into T FH 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 T FH cells.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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