Literature DB >> 28279590

Transcription Factor T-bet Orchestrates Lineage Development and Function in the Immune System.

Axel Kallies1, Kim L Good-Jacobson2.   

Abstract

T-bet was originally described as the key transcription factor defining type 1 T helper (Th) cells. However, it is now clear that it drives the orchestrated generation of effector and memory cells in multiple different lymphocyte lineages. In addition to Th1 cells, CD8 T cells, B cells and some innate lymphocyte populations require T-bet for their development or differentiation in response to antigen. Furthermore, other Th cell populations, including T follicular helper and Th17, as well as regulatory T cells can co-opt T-bet expression to promote functional diversification and colocalization. Thus, T-bet broadly regulates transcriptional programs in response to type 1 inflammatory signals and mediates the coordinated differentiation, function, migration and survival of effector and memory lymphocyte subsets in the affected tissue. Therefore, T-bet expression is essential for effective clearance of pathogens and maintenance of immunity. Crown
Copyright © 2017. Published by Elsevier Ltd. All rights reserved.

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Year:  2017        PMID: 28279590     DOI: 10.1016/j.it.2017.02.003

Source DB:  PubMed          Journal:  Trends Immunol        ISSN: 1471-4906            Impact factor:   16.687


  54 in total

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