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Keratinocyte-intrinsic MHCII expression controls microbiota-induced Th1 cell responses.

Samira TamoutounourSeong-Ji HanJulie DeckersMichael G ConstantinidesCharlotte HurabielleOliver J HarrisonNicolas BouladouxJonathan L LinehanVerena M LinkIvan Vujkovic-CvijinPaula Juliana Perez-ChaparroStephan P RosshartBarbara RehermannVanja LazarevicYasmine Belkaid
Published in: Proceedings of the National Academy of Sciences of the United States of America (2019)
The cross-talk between the microbiota and the immune system plays a fundamental role in the control of host physiology. However, the tissue-specific factors controlling this dialogue remain poorly understood. Here we demonstrate that T cell responses to commensal colonization are associated with the development of organized cellular clusters within the skin epithelium. These organized lymphocyte clusters are surrounded by keratinocytes expressing a discrete program associated with antigen presentation and antimicrobial defense. Notably, IL-22-mediated keratinocyte-intrinsic MHC class II expression was required for the selective accumulation of commensal-induced IFN-γ, but not IL-17A-producing CD4+ T cells within the skin. Taking these data together, this work uncovers an unexpected role for MHC class II expression by keratinocytes in the control of homeostatic type 1 responses to the microbiota. Our findings have important implications for the understanding of the tissue-specific rules governing the dialogue between a host and its microbiota.
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