Molecular control of tissue-resident regulatory T cell differentiation (#42)
Non-lymphoid tissues harbor a broad spectrum of immune cells that directly contribute to the control of local immunity. Additionally, these cells are also involved in non-canonical functions including tissue repair and regulation of metabolism. Regulatory T (Treg) cells play a central role in restraining inflammatory parameters in the tissue and thereby limit immune-mediated pathology and maintain tissue homeostasis. We have demonstrated previously that adipose tissue-resident Treg cells specifically depend on interleukin (IL)-33 for their survival and maintenance. Furthermore, we have shown that the transcription factor IRF4 controls an adipose-tissue specific transcriptional module including expression of the IL-33 receptor, which is critical for the differentiation of adipose tissue-resident Treg cells. We have now extended our studies and investigated how other factors control Treg cells resident in non-lymphoid tissues such as the gastrointestinal tract. Overall, our work shows that tissue Treg cells constitute diverse, highly specialised populations of regulatory T cells that are exquisitely sensitive to differences in their tissue niche.