IgA production requires B cell interaction with subepithelial dendritic cells in Peyer’s patches
Author(s) -
Andrea Reboldi,
Tal I. Ar,
Lauren B. Rodda,
Amha Atakilit,
Dean Sheppard,
Jason G. Cyster
Publication year - 2016
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aaf4822
Subject(s) - peyer's patch , immunology , c c chemokine receptor type 6 , immunoglobulin class switching , follicular dendritic cells , biology , dendritic cell , lymphotoxin , immunoglobulin a , transforming growth factor , chemokine , antibody , chemokine receptor , microbiology and biotechnology , t cell , b cell , immune system , antigen presenting cell , immunoglobulin g
Immunoglobulin A (IgA) induction primarily occurs in intestinal Peyer's patches (PPs). However, the cellular interactions necessary for IgA class switching are poorly defined. Here we show that in mice, activated B cells use the chemokine receptor CCR6 to access the subepithelial dome (SED) of PPs. There, B cells undergo prolonged interactions with SED dendritic cells (DCs). PP IgA class switching requires innate lymphoid cells, which promote lymphotoxin-β receptor (LTβR)-dependent maintenance of DCs. PP DCs augment IgA production by integrin avb8-mediated activation of transforming growth factor-β (TGFβ). In mice where B cells cannot access the SED, IgA responses against oral antigen and gut commensals are impaired. These studies establish the PP SED as a niche supporting DC-B cell interactions needed for TGFβ activation and induction of mucosal IgA responses
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