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Effects of Non-Coding RNA on Regulatory T Cells and Implications for Treatment of Immunological Diseases

Regulatory T cells (Tregs) are essential for regulating immune reactions and maintaining immune homeostasis. Non-coding RNAs (ncRNAs), including microRNAs and long non-coding RNAs, usually do not encode proteins but regulate intracellular biological processes at post-transcriptional levels. These nc...

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Detalles Bibliográficos
Autores principales: Luo, Yuanhanyu, Wang, Honglin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714939/
https://www.ncbi.nlm.nih.gov/pubmed/33329608
http://dx.doi.org/10.3389/fimmu.2020.612060
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author Luo, Yuanhanyu
Wang, Honglin
author_facet Luo, Yuanhanyu
Wang, Honglin
author_sort Luo, Yuanhanyu
collection PubMed
description Regulatory T cells (Tregs) are essential for regulating immune reactions and maintaining immune homeostasis. Non-coding RNAs (ncRNAs), including microRNAs and long non-coding RNAs, usually do not encode proteins but regulate intracellular biological processes at post-transcriptional levels. These ncRNAs have been demonstrated as key post-transcriptional regulators in the commitment of Tregs lineage and the plasticity of Tregs function. These ncRNAs can further be manipulated to benefit human immunological disorders caused by Tregs dysfunction. This review summarizes the effects of ncRNAs on Tregs and their potentials to be targets or approaches for the treatment of immunological diseases involving Tregs.
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spelling pubmed-77149392020-12-15 Effects of Non-Coding RNA on Regulatory T Cells and Implications for Treatment of Immunological Diseases Luo, Yuanhanyu Wang, Honglin Front Immunol Immunology Regulatory T cells (Tregs) are essential for regulating immune reactions and maintaining immune homeostasis. Non-coding RNAs (ncRNAs), including microRNAs and long non-coding RNAs, usually do not encode proteins but regulate intracellular biological processes at post-transcriptional levels. These ncRNAs have been demonstrated as key post-transcriptional regulators in the commitment of Tregs lineage and the plasticity of Tregs function. These ncRNAs can further be manipulated to benefit human immunological disorders caused by Tregs dysfunction. This review summarizes the effects of ncRNAs on Tregs and their potentials to be targets or approaches for the treatment of immunological diseases involving Tregs. Frontiers Media S.A. 2020-11-20 /pmc/articles/PMC7714939/ /pubmed/33329608 http://dx.doi.org/10.3389/fimmu.2020.612060 Text en Copyright © 2020 Luo and Wang http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Luo, Yuanhanyu
Wang, Honglin
Effects of Non-Coding RNA on Regulatory T Cells and Implications for Treatment of Immunological Diseases
title Effects of Non-Coding RNA on Regulatory T Cells and Implications for Treatment of Immunological Diseases
title_full Effects of Non-Coding RNA on Regulatory T Cells and Implications for Treatment of Immunological Diseases
title_fullStr Effects of Non-Coding RNA on Regulatory T Cells and Implications for Treatment of Immunological Diseases
title_full_unstemmed Effects of Non-Coding RNA on Regulatory T Cells and Implications for Treatment of Immunological Diseases
title_short Effects of Non-Coding RNA on Regulatory T Cells and Implications for Treatment of Immunological Diseases
title_sort effects of non-coding rna on regulatory t cells and implications for treatment of immunological diseases
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714939/
https://www.ncbi.nlm.nih.gov/pubmed/33329608
http://dx.doi.org/10.3389/fimmu.2020.612060
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