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Genomic and Transcriptional Mechanisms Governing Innate-like T Lymphocyte Development
Author(s) -
Roxroy C. Morgan,
Barbara L. Kee
Publication year - 2022
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.2200141
Subject(s) - innate lymphoid cell , biology , innate immune system , effector , cytotoxic t cell , immunology , transcription factor , function (biology) , chromatin , proinflammatory cytokine , microbiology and biotechnology , immune system , inflammation , genetics , gene , in vitro
Innate-like lymphocytes are a subset of lymphoid cells that function as a first line of defense against microbial infection. These cells are activated by proinflammatory cytokines or broadly expressed receptors and are able to rapidly perform their effector functions owing to a uniquely primed chromatin state that is acquired as a part of their developmental program. These cells function in many organs to protect against disease, but they release cytokines and cytotoxic mediators that can also lead to severe tissue pathologies. Therefore, harnessing the capabilities of these cells for therapeutic interventions will require a deep understanding of how these cells develop and regulate their effector functions. In this review we discuss recent advances in the identification of the transcription factors and the genomic regions that guide the development and function of invariant NKT cells and we highlight related mechanisms in other innate-like lymphocytes.

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