Regulation of γδ T Cell Effector Diversification in the Thymus.

Front Immunol

Department of Immunology, Duke University Medical Center, Durham, NC, United States.

Published: February 2021

AI Article Synopsis

  • γδ T cells develop in the thymus earlier than αβ T cells and can quickly produce effector cytokines to defend barriers in various tissues.
  • Unlike αβ T cells that leave the thymus as naïve, γδ T cells are primed for action during development.
  • This review focuses on the factors influencing the effector functions of γδ T cells, including the T cell receptor, environmental cues, and transcription factors, highlighting their importance in immunity and disease.

Article Abstract

γδ T cells are the first T cell lineage to develop in the thymus and take up residence in a wide variety of tissues where they can provide fast, innate-like sources of effector cytokines for barrier defense. In contrast to conventional αβ T cells that egress the thymus as naïve cells, γδ T cells can be programmed for effector function during development in the thymus. Understanding the molecular mechanisms that determine γδ T cell effector fate is of great interest due to the wide-spread tissue distribution of γδ T cells and their roles in pathogen clearance, immunosurveillance, cancer, and autoimmune diseases. In this review, we will integrate the current understanding of the role of the T cell receptor, environmental signals, and transcription factor networks in controlling mouse innate-like γδ T cell effector commitment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992645PMC
http://dx.doi.org/10.3389/fimmu.2020.00042DOI Listing

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