Transforming growth factor–β1 in regulatory T cell biology

Author:

Moreau Joshua M.1ORCID,Velegraki Maria2ORCID,Bolyard Chelsea2,Rosenblum Michael D.1ORCID,Li Zihai2ORCID

Affiliation:

1. Department of Dermatology, University of California, San Francisco, San Francisco, CA, USA.

2. Pelotonia Institute for Immuno-Oncology, the Ohio State University Comprehensive Cancer Center—James Cancer Hospital, Columbus, OH, USA.

Abstract

Transforming growth factor–β1 (TGF-β1) is inextricably linked to regulatory T cell (T reg ) biology. However, precisely untangling the role for TGF-β1 in T reg differentiation and function is complicated by the pleiotropic and context-dependent activity of this cytokine and the multifaceted biology of T regs . Among CD4 + T cells, T regs are the major producers of latent TGF-β1 and are uniquely able to activate this cytokine via expression of cell surface docking receptor glycoprotein A repetitions predominant (GARP) and αv integrins. Although a preponderance of evidence indicates no essential roles for T reg -derived TGF-β1 in T reg immunosuppression, TGF-β1 signaling is crucial for T reg development in the thymus and periphery. Furthermore, active TGF-β1 instructs the differentiation of other T cell subsets, including T H 17 cells. Here, we will review TGF-β1 signaling in T reg development and function and discuss knowledge gaps, future research, and the TGF-β1/T reg axis in the context of cancer immunotherapy and fibrosis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine,Immunology

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