Keratinocyte-intrinsic MHCII expression controls microbiota-induced Th1 cell responses.
basic_science · Level V
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- Record sourced from PubMed, PMID 31672911.
- Also identified by DOI 10.1073/pnas.1912432116 and PMC identifier 6876208.
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Abstract
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<sup>+</sup> 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.
Medical subject headings
- Epidermis
- Histocompatibility Antigens Class II
- Host Microbial Interactions
- Keratinocytes
- Microbiota
- Th1 Cells