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Control of Lymphocyte Fate, Infection, and Tumor Immunity by TCF-1

T cell factor-1 (TCF-1), encoded by Tcf7, is a transcription factor and histone deacetylase (HDAC) essential for commitment to both the T cell and the innate lymphoid cell (ILC) lineages in mammals. In this review, we discuss the multifunctional role of TCF-1 in establishing these lineages and the r...

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Bibliographic Details
Published in:Trends in immunology 2019-12, Vol.40 (12), p.1149-1162
Main Authors: Raghu, Dinesh, Xue, Hai-Hui, Mielke, Lisa A.
Format: Article
Language:English
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Summary:T cell factor-1 (TCF-1), encoded by Tcf7, is a transcription factor and histone deacetylase (HDAC) essential for commitment to both the T cell and the innate lymphoid cell (ILC) lineages in mammals. In this review, we discuss the multifunctional role of TCF-1 in establishing these lineages and the requirement for TCF-1 throughout lineage differentiation and maintenance of lineage stability. We highlight recent reports showing promise for TCF-1 as a novel biomarker to identify recently characterized subsets of exhausted CD8+ T cells that may help to predict patient responses to immune checkpoint blockade (ICB). T cell factor-1 (TCF-1) acts as a transcription factor and histone deacetylase (HDAC) in both mouse and humans to shape innate and adaptive immunity.Expression of TCF-1 is necessary for the development of ILC progenitor cells in mouse bone marrow.In murine T cell development, TCF-1 is critical for ETP development, commitment to the CD4+ T cell lineage, and stabilization of CD8+ T cells by suppressing alternative fate differentiation.Increased TCF-1 expression is important for the development of central memory CD8+ T cells that provide long-term protection following acute viral infection in mice.TCF-1 is critical for the development of Tex-stem cells that replenish Tex-term cells following chronic viral infection and in response to tumor formation. The presence of Tex-stem cells can be predictive of good prognosis in various cancer types and help to mediate patient responses to ICB.
ISSN:1471-4906
1471-4981
DOI:10.1016/j.it.2019.10.006