| Literature DB >> 30366517 |
Hidetoshi Nakagawa1, Lei Wang1, Harvey Cantor2, Hye-Jung Kim1.
Abstract
Regulatory T cells are central mediators of immune regulation and play an essential role in the maintenance of immune homeostasis in the steady state and under pathophysiological conditions. Disruption of CD8 Treg-dependent recognition of Qa-1-restricted self-antigens can result in dysregulated immune responses, tissue damage, autoimmune disease and cancer. Recent progress in studies on regulatory T cells of the CD8 lineage has provided new biological insight into this specialized regulatory T cell subpopulation. Identification of the Helios transcription factor as an essential control element for the differentiation and function of CD8 regulatory T cells has led to a better understanding of the unique genetic program of these cells. Recent analyses of T-cell receptor usage and antigen recognition by Qa-1-restricted CD8 Treg have provided additional insight into the unusual biological function of this regulatory CD8 lineage. Here we summarize recent advances in our understanding of CD8 regulatory T cells with emphasis on lineage commitment, differentiation and stability.Entities:
Keywords: Helios; Inflammation; Qa-1; Suppression; Treg lineage commitment; Treg lineage stability; Tumor microenvironment
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Year: 2018 PMID: 30366517 DOI: 10.1016/bs.ai.2018.09.001
Source DB: PubMed Journal: Adv Immunol ISSN: 0065-2776 Impact factor: 3.543