Regulation of humoral and cellular gut immunity by lamina propria dendritic cells expressing Toll-like receptor 5

S Uematsu, K Fujimoto, MH Jang, BG Yang… - Nature …, 2008 - nature.com
S Uematsu, K Fujimoto, MH Jang, BG Yang, YJ Jung, M Nishiyama, S Sato, T Tsujimura…
Nature immunology, 2008nature.com
The intestinal cell types responsible for defense against pathogenic organisms remain
incompletely characterized. Here we identify a subset of CD11chiCD11bhi lamina propria
dendritic cells (LPDCs) that expressed Toll-like receptor 5 (TLR5) in the small intestine.
When stimulated by the TLR5 ligand flagellin, TLR5+ LPDCs induced the differentiation of
naive B cells into immunoglobulin A–producing plasma cells by a mechanism independent
of gut-associated lymphoid tissue. In addition, by a mechanism dependent on TLR5 …
Abstract
The intestinal cell types responsible for defense against pathogenic organisms remain incompletely characterized. Here we identify a subset of CD11chiCD11bhi lamina propria dendritic cells (LPDCs) that expressed Toll-like receptor 5 (TLR5) in the small intestine. When stimulated by the TLR5 ligand flagellin, TLR5+ LPDCs induced the differentiation of naive B cells into immunoglobulin A–producing plasma cells by a mechanism independent of gut-associated lymphoid tissue. In addition, by a mechanism dependent on TLR5 stimulation, these LPDCs promoted the differentiation of antigen-specific interleukin 17–producing T helper cells and type 1 T helper cells. Unlike spleen DCs, the LPDCs specifically produced retinoic acid, which, in a dose-dependent way, supported the generation and retention of immunoglobulin A–producing cells in the lamina propria and positively regulated the differentiation interleukin 17–producing T helper cells. Our findings demonstrate unique properties of LPDCs and the importance of TLR5 for adaptive immunity in the intestine.
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