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Publication : IL-22-dependent dysbiosis and mononuclear phagocyte depletion contribute to steroid-resistant gut graft-versus-host disease in mice.

First Author  Song Q Year  2021
Journal  Nat Commun Volume  12
Issue  1 Pages  805
PubMed ID  33547295 Mgi Jnum  J:302514
Mgi Id  MGI:6508190 Doi  10.1038/s41467-021-21133-3
Citation  Song Q, et al. (2021) IL-22-dependent dysbiosis and mononuclear phagocyte depletion contribute to steroid-resistant gut graft-versus-host disease in mice. Nat Commun 12(1):805
abstractText  Efforts to improve the prognosis of steroid-resistant gut acute graft-versus-host-disease (SR-Gut-aGVHD) have suffered from poor understanding of its pathogenesis. Here we show that the pathogenesis of SR-Gut-aGVHD is associated with reduction of IFN-gamma(+) Th/Tc1 cells and preferential expansion of IL-17(-)IL-22(+) Th/Tc22 cells. The IL-22 from Th/Tc22 cells causes dysbiosis in a Reg3gamma-dependent manner. Transplantation of IFN-gamma-deficient donor CD8(+) T cells in the absence of CD4(+) T cells produces a phenocopy of SR-Gut-aGVHD. IFN-gamma deficiency in donor CD8(+) T cells also leads to a PD-1-dependent depletion of intestinal protective CX3CR1(hi) mononuclear phagocytes (MNP), which also augments expansion of Tc22 cells. Supporting the dual regulation, simultaneous dysbiosis induction and depletion of CX3CR1(hi) MNP results in full-blown Gut-aGVHD. Our results thus provide insights into SR-Gut-aGVHD pathogenesis and suggest the potential efficacy of IL-22 antagonists and IFN-gamma agonists in SR-Gut-aGVHD therapy.
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