TY - JOUR
T1 - The Roles of Peyer's Patches and Microfold Cells in the Gut Immune System
T2 - Relevance to Autoimmune Diseases
AU - Kobayashi, Nobuhide
AU - Takahashi, Daisuke
AU - Takano, Shunsuke
AU - Kimura, Shunsuke
AU - Hase, Koji
N1 - Funding Information:
Funding. This study was supported by grants from the Japan Society for the Promotion of Science (#16H01369, 17KT0055, and 18H04680 to KH), Health Labour Sciences Research Grant (KH), AMED-Crest (#16gm0000000h0101, 17gm1010004h0102, and 18gm1010004h0103 to KH), Yakult Foundation (KH), The Aashi Grass Foundation (KH), and Kobayashi Foundation (KH).
Publisher Copyright:
© Copyright © 2019 Kobayashi, Takahashi, Takano, Kimura and Hase.
PY - 2019/10/9
Y1 - 2019/10/9
N2 - Microfold (M) cells are located in the epithelium covering mucosa-associated lymphoid tissues, such as the Peyer's patches (PPs) of the small intestine. M cells actively transport luminal antigens to the underlying lymphoid follicles to initiate an immune response. The molecular machinery of M-cell differentiation and function has been vigorously investigated over the last decade. Studies have shed light on the role of M cells in the mucosal immune system and have revealed that antigen uptake by M cells contributes to not only mucosal but also systemic immune responses. However, M-cell studies usually focus on infectious diseases; the contribution of M cells to autoimmune diseases has remained largely unexplored. Accumulating evidence suggests that dysbiosis of the intestinal microbiota is implicated in multiple systemic diseases, including autoimmune diseases. This implies that the uptake of microorganisms by M cells in PPs may play a role in the pathogenesis of autoimmune diseases. We provide an outline of the current understanding of M-cell biology and subsequently discuss the potential contribution of M cells and PPs to the induction of systemic autoimmunity, beyond the mucosal immune response.
AB - Microfold (M) cells are located in the epithelium covering mucosa-associated lymphoid tissues, such as the Peyer's patches (PPs) of the small intestine. M cells actively transport luminal antigens to the underlying lymphoid follicles to initiate an immune response. The molecular machinery of M-cell differentiation and function has been vigorously investigated over the last decade. Studies have shed light on the role of M cells in the mucosal immune system and have revealed that antigen uptake by M cells contributes to not only mucosal but also systemic immune responses. However, M-cell studies usually focus on infectious diseases; the contribution of M cells to autoimmune diseases has remained largely unexplored. Accumulating evidence suggests that dysbiosis of the intestinal microbiota is implicated in multiple systemic diseases, including autoimmune diseases. This implies that the uptake of microorganisms by M cells in PPs may play a role in the pathogenesis of autoimmune diseases. We provide an outline of the current understanding of M-cell biology and subsequently discuss the potential contribution of M cells and PPs to the induction of systemic autoimmunity, beyond the mucosal immune response.
KW - Peyer's patch
KW - autoimmune disease
KW - intestinal epithelial cell
KW - intestinal microbiota
KW - microfold cell
KW - mucosal immunity
UR - http://www.scopus.com/inward/record.url?scp=85074067478&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85074067478&partnerID=8YFLogxK
U2 - 10.3389/fimmu.2019.02345
DO - 10.3389/fimmu.2019.02345
M3 - Review article
C2 - 31649668
AN - SCOPUS:85074067478
SN - 1664-3224
VL - 10
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 2345
ER -