Key result
Tissue regulatory T cells adapt locally to promote organ maintenance, regeneration, and repair across non-lymphoid tissues.
Treg cells have been initially described as gatekeepers for the control of autoimmunity, as they can actively suppress the activity of other immune cells. However, their role goes beyond this as Treg cells further control immune responses during infections and tumor development. Furthermore, Treg cells can acquire additional properties for e.g., the control of tissue homeostasis. This is instructed by a specific differentiation program and the acquisition of effector properties unique to Treg cells in non-lymphoid tissues. These tissue Treg cells can further adapt to their tissue environment and acquire distinct functional properties through specific transcription factors activated by a combination of tissue derived factors, including tissue-specific antigens and cytokines. In this review, we will focus on recent findings extending our current understanding of the role and differentiation of these tissue Treg cells. As such we will highlight the importance of tissue Treg cells for tissue maintenance, regeneration, and repair in adipose tissue, muscle, CNS, liver, kidney, reproductive organs, and the lung.
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Malko et al. (2022) conducted a review in Tissue homeostasis and pathophysiology. Tissue regulatory T cells (Tregs) was evaluated. Tissue regulatory T cells adapt to their environment and regulate tissue maintenance, regeneration, and repair in non-lymphoid tissues such as adipose, muscle, CNS, liver, kidney, and lung.
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