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Spatial distribution of LTi-like cells in intestinal mucosa regulates type 3 innate immunity.


ABSTRACT: Lymphoid tissue inducer (LTi)-like cells are tissue resident innate lymphocytes that rapidly secrete cytokines that promote gut epithelial integrity and protect against extracellular bacterial infections.Here, we report that the retention of LTi-like cells in conventional solitary intestinal lymphoid tissue (SILT) is essential for controlling LTi-like cell function and is maintained by expression of the chemokine receptor CXCR5. Deletion of Cxcr5 functionally unleashed LTi-like cells in a cell intrinsic manner, leading to uncontrolled IL-17 and IL-22 production. The elevated production of IL-22 in Cxcr5-deficient mice improved gut barrier integrity and protected mice during infection with the opportunistic pathogen Clostridium difficile Interestingly, Cxcr5-/- mice developed LTi-like cell aggregates that were displaced from their typical niche at the intestinal crypt, and LTi-like cell hyperresponsiveness was associated with the local formation of this unconventional SILT. Thus, LTi-like cell positioning within mucosa controls their activity via niche-specific signals that temper cytokine production during homeostasis.

SUBMITTER: Secca C 

PROVIDER: S-EPMC8201890 | biostudies-literature | 2021 Jun

REPOSITORIES: biostudies-literature

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Spatial distribution of LTi-like cells in intestinal mucosa regulates type 3 innate immunity.

Sécca Cristiane C   Bando Jennifer K JK   Fachi José L JL   Gilfillan Susan S   Peng Vincent V   Di Luccia Blanda B   Cella Marina M   McDonald Keely G KG   Newberry Rodney D RD   Colonna Marco M  

Proceedings of the National Academy of Sciences of the United States of America 20210601 23


Lymphoid tissue inducer (LTi)-like cells are tissue resident innate lymphocytes that rapidly secrete cytokines that promote gut epithelial integrity and protect against extracellular bacterial infections.Here, we report that the retention of LTi-like cells in conventional solitary intestinal lymphoid tissue (SILT) is essential for controlling LTi-like cell function and is maintained by expression of the chemokine receptor CXCR5. Deletion of <i>Cxcr5</i> functionally unleashed LTi-like cells in a  ...[more]

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