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Targeting Regulatory T Cells to Treat Patients With Systemic Lupus Erythematosus

Regulatory T cells (Tregs) are central in integration and maintenance of immune homeostasis. Since breakdown of self-tolerance is a major culprit in the pathogenesis of systemic lupus erythematosus (SLE), restoration of the immune tolerance through the manipulation of Tregs can be exploited to treat...

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Detalles Bibliográficos
Autores principales: Mizui, Masayuki, Tsokos, George C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932391/
https://www.ncbi.nlm.nih.gov/pubmed/29755456
http://dx.doi.org/10.3389/fimmu.2018.00786
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author Mizui, Masayuki
Tsokos, George C.
author_facet Mizui, Masayuki
Tsokos, George C.
author_sort Mizui, Masayuki
collection PubMed
description Regulatory T cells (Tregs) are central in integration and maintenance of immune homeostasis. Since breakdown of self-tolerance is a major culprit in the pathogenesis of systemic lupus erythematosus (SLE), restoration of the immune tolerance through the manipulation of Tregs can be exploited to treat patients with SLE. New information has revealed that Tregs besides their role in suppressing the immune response are important in tissue protection and regeneration. Expansion of Tregs with low-dose IL-2 represents an approach to control the autoimmune response. Moreover, control of Treg metabolism can be exploited to restore or improve their function. Here, we summarize the function and diversity of Tregs and recent strategies to improve their function in patients with SLE.
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spelling pubmed-59323912018-05-11 Targeting Regulatory T Cells to Treat Patients With Systemic Lupus Erythematosus Mizui, Masayuki Tsokos, George C. Front Immunol Immunology Regulatory T cells (Tregs) are central in integration and maintenance of immune homeostasis. Since breakdown of self-tolerance is a major culprit in the pathogenesis of systemic lupus erythematosus (SLE), restoration of the immune tolerance through the manipulation of Tregs can be exploited to treat patients with SLE. New information has revealed that Tregs besides their role in suppressing the immune response are important in tissue protection and regeneration. Expansion of Tregs with low-dose IL-2 represents an approach to control the autoimmune response. Moreover, control of Treg metabolism can be exploited to restore or improve their function. Here, we summarize the function and diversity of Tregs and recent strategies to improve their function in patients with SLE. Frontiers Media S.A. 2018-04-17 /pmc/articles/PMC5932391/ /pubmed/29755456 http://dx.doi.org/10.3389/fimmu.2018.00786 Text en Copyright © 2018 Mizui and Tsokos. https://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 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
Mizui, Masayuki
Tsokos, George C.
Targeting Regulatory T Cells to Treat Patients With Systemic Lupus Erythematosus
title Targeting Regulatory T Cells to Treat Patients With Systemic Lupus Erythematosus
title_full Targeting Regulatory T Cells to Treat Patients With Systemic Lupus Erythematosus
title_fullStr Targeting Regulatory T Cells to Treat Patients With Systemic Lupus Erythematosus
title_full_unstemmed Targeting Regulatory T Cells to Treat Patients With Systemic Lupus Erythematosus
title_short Targeting Regulatory T Cells to Treat Patients With Systemic Lupus Erythematosus
title_sort targeting regulatory t cells to treat patients with systemic lupus erythematosus
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932391/
https://www.ncbi.nlm.nih.gov/pubmed/29755456
http://dx.doi.org/10.3389/fimmu.2018.00786
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