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Skin IL-17-Producing T Cells Support Repair 2!
Daniel F Zegarra-Ruiz1, Gretchen E Diehl2
1Alkek Center for Metagenomics and Microbiome Research, and Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX 77030, USA.
Trends in Immunology
|February 6, 2019
Summary
Skin T cells expressing RORγt act as sentinels, rapidly producing type 2 T helper cell (Th2) cytokines after tissue injury. These cells link commensal recognition, damage, and wound repair in mice.
Area of Science:
- Immunology
- Dermatology
- Microbiology
Background:
- Skin commensals play a role in immune system regulation.
- T cells are crucial for adaptive immunity and tissue homeostasis.
- RORγt is a transcription factor involved in T cell differentiation.
Purpose of the Study:
- To investigate the role of RORγt-expressing T cells in response to skin wounding.
- To understand the function of commensal-specific T cells in tissue repair.
- To explore the link between microbial recognition and wound healing.
Main Methods:
- Studied mice models with specific T cell populations.
- Analyzed cytokine production and gene expression in T cells after induced skin injury.
- Utilized techniques to track T cell responses to commensals and tissue damage.
Main Results:
- RORγt-expressing skin commensal-specific T cells rapidly produced type 2 T helper cell (Th2) cytokines upon wounding.
- These T cells constitutively coexpressed GATA-3 and type 2 cytokine mRNAs, which were translated post-injury.
- Demonstrated that these T cells function as sentinels, connecting T cell receptor (TCR) recognition of commensals with tissue damage and repair processes.
Conclusions:
- RORγt+ T cells serve as critical sentinels in the skin.
- These cells integrate signals from commensal microbes and tissue injury to modulate wound repair.
- Highlights a novel mechanism linking innate and adaptive immunity in skin homeostasis and repair.
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