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Publication : A RORγt(+) cell instructs gut microbiota-specific T(reg) cell differentiation.

First Author  Kedmi R Year  2022
Journal  Nature Volume  610
Issue  7933 Pages  737-743
PubMed ID  36071167 Mgi Jnum  J:339994
Mgi Id  MGI:7525445 Doi  10.1038/s41586-022-05089-y
Citation  Kedmi R, et al. (2022) A RORgammat(+) cell instructs gut microbiota-specific T(reg) cell differentiation. Nature 610(7933):737-743
abstractText  The mutualistic relationship of gut-resident microbiota and the host immune system promotes homeostasis that ensures maintenance of the microbial community and of a largely non-aggressive immune cell compartment(1,2). The consequences of disturbing this balance include proximal inflammatory conditions, such as Crohn's disease, and systemic illnesses. This equilibrium is achieved in part through the induction of both effector and suppressor arms of the adaptive immune system. Helicobacter species induce T regulatory (T(reg)) and T follicular helper (T(FH)) cells under homeostatic conditions, but induce inflammatory T helper 17 (T(H)17) cells when induced T(reg) (iT(reg)) cells are compromised(3,4). How Helicobacter and other gut bacteria direct T cells to adopt distinct functions remains poorly understood. Here we investigated the cells and molecular components required for iT(reg) cell differentiation. We found that antigen presentation by cells expressing RORgammat, rather than by classical dendritic cells, was required and sufficient for induction of T(reg) cells. These RORgammat(+) cells-probably type 3 innate lymphoid cells and/or Janus cells(5)-require the antigen-presentation machinery, the chemokine receptor CCR7 and the TGFbeta activator alpha(v) integrin. In the absence of any of these factors, there was expansion of pathogenic T(H)17 cells instead of iT(reg) cells, induced by CCR7-independent antigen-presenting cells. Thus, intestinal commensal microbes and their products target multiple antigen-presenting cells with pre-determined features suited to directing appropriate T cell differentiation programmes, rather than a common antigen-presenting cell that they endow with appropriate functions.
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