Matches in SemOpenAlex for { <https://semopenalex.org/work/W3202078153> ?p ?o ?g. }
- W3202078153 abstract "The concept that a subset of T cells exists that specifically suppresses immune responses was originally proposed over 50 years ago. It then took the next 30 years to solidify the concept of regulatory T cells (Tregs) into the paradigm we understand today – namely a subset of CD4+ FOXP3+ T-cells that are critical for controlling immune responses to self and commensal or environmental antigens that also play key roles in promoting tissue homeostasis and repair. Expression of the transcription factor FOXP3 is a defining feature of Tregs, while the cytokine IL2 is necessary for robust Treg development and function. While our initial conception of Tregs was as a monomorphic lineage required to suppress all types of immune responses, recent work has demonstrated extensive phenotypic and functional diversity within the Treg population. In this review we address the ontogeny, phenotype, and function of the large number of distinct effector Treg subsets that have been defined over the last 15 years." @default.
- W3202078153 created "2021-10-11" @default.
- W3202078153 creator A5003724636 @default.
- W3202078153 creator A5056756483 @default.
- W3202078153 creator A5059124560 @default.
- W3202078153 creator A5074975950 @default.
- W3202078153 date "2021-09-23" @default.
- W3202078153 modified "2023-10-16" @default.
- W3202078153 title "Phenotypic and Functional Diversity in Regulatory T Cells" @default.
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