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Publication : Resident T(H)2 cells orchestrate adipose tissue remodeling at a site adjacent to infection.

First Author  Kabat AM Year  2022
Journal  Sci Immunol Volume  7
Issue  76 Pages  eadd3263
PubMed ID  36240286 Mgi Jnum  J:355192
Mgi Id  MGI:7737839 Doi  10.1126/sciimmunol.add3263
Citation  Kabat AM, et al. (2022) Resident T(H)2 cells orchestrate adipose tissue remodeling at a site adjacent to infection. Sci Immunol 7(76):eadd3263
abstractText  Type 2 immunity is associated with adipose tissue (AT) homeostasis and infection with parasitic helminths, but whether AT participates in immunity to these parasites is unknown. We found that the fat content of mesenteric AT (mAT) declined in mice during infection with a gut-restricted helminth. This was associated with the accumulation of metabolically activated, interleukin-33 (IL-33), thymic stromal lymphopoietin (TSLP), and extracellular matrix (ECM)-producing stromal cells. These cells shared transcriptional features, including the expression of Dpp4 and Pi16, with multipotent progenitor cells (MPC) that have been identified in numerous tissues and are reported to be capable of differentiating into fibroblasts and adipocytes. Concomitantly, mAT became infiltrated with resident T helper 2 (T(H)2) cells that responded to TSLP and IL-33 by producing stromal cell-stimulating cytokines, including transforming growth factor beta1 (TGFbeta(1)) and amphiregulin. These T(H)2 cells expressed genes previously associated with type 2 innate lymphoid cells (ILC2), including Nmur1, Calca, Klrg1, and Arg1, and persisted in mAT for at least 11 months after anthelmintic drug-mediated clearance of infection. We found that MPC and T(H)2 cells localized to ECM-rich interstitial spaces that appeared shared between mesenteric lymph node, mAT, and intestine. Stromal cell expression of epidermal growth factor receptor (EGFR), the receptor for amphiregulin, was required for immunity to infection. Our findings point to the importance of MPC and T(H)2 cell interactions within the interstitium in orchestrating AT remodeling and immunity to an intestinal infection.
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