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Harnessing CD8(+)CD28(−) Regulatory T Cells as a Tool to Treat Autoimmune Disease

T regulatory cell therapy presents a novel therapeutic strategy for patients with autoimmune diseases or who are undergoing transplantation. At present, the CD4(+) Treg population has been extensively characterized, as a result of defined phenotypic and functional readouts. In this review article, w...

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Detalles Bibliográficos
Autores principales: Ceeraz, Sabrina, Thompson, Charlotte R., Beatson, Richard, Choy, Ernest H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616472/
https://www.ncbi.nlm.nih.gov/pubmed/34831195
http://dx.doi.org/10.3390/cells10112973
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author Ceeraz, Sabrina
Thompson, Charlotte R.
Beatson, Richard
Choy, Ernest H.
author_facet Ceeraz, Sabrina
Thompson, Charlotte R.
Beatson, Richard
Choy, Ernest H.
author_sort Ceeraz, Sabrina
collection PubMed
description T regulatory cell therapy presents a novel therapeutic strategy for patients with autoimmune diseases or who are undergoing transplantation. At present, the CD4(+) Treg population has been extensively characterized, as a result of defined phenotypic and functional readouts. In this review article, we discuss the development and biology of CD8(+) Tregs and their role in murine and human disease indications. A subset of CD8(+) Tregs that lack the surface expression of CD28 (CD8(+)CD28(−) Treg) has proved efficacious in preclinical models. CD8(+)CD28(−) Tregs are present in healthy individuals, but their impaired functionality in disease renders them less effective in mediating immunosuppression. We primarily focus on harnessing CD8(+) Treg cell therapy in the clinic to support current treatment for patients with autoimmune or inflammatory conditions.
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spelling pubmed-86164722021-11-26 Harnessing CD8(+)CD28(−) Regulatory T Cells as a Tool to Treat Autoimmune Disease Ceeraz, Sabrina Thompson, Charlotte R. Beatson, Richard Choy, Ernest H. Cells Review T regulatory cell therapy presents a novel therapeutic strategy for patients with autoimmune diseases or who are undergoing transplantation. At present, the CD4(+) Treg population has been extensively characterized, as a result of defined phenotypic and functional readouts. In this review article, we discuss the development and biology of CD8(+) Tregs and their role in murine and human disease indications. A subset of CD8(+) Tregs that lack the surface expression of CD28 (CD8(+)CD28(−) Treg) has proved efficacious in preclinical models. CD8(+)CD28(−) Tregs are present in healthy individuals, but their impaired functionality in disease renders them less effective in mediating immunosuppression. We primarily focus on harnessing CD8(+) Treg cell therapy in the clinic to support current treatment for patients with autoimmune or inflammatory conditions. MDPI 2021-11-01 /pmc/articles/PMC8616472/ /pubmed/34831195 http://dx.doi.org/10.3390/cells10112973 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ceeraz, Sabrina
Thompson, Charlotte R.
Beatson, Richard
Choy, Ernest H.
Harnessing CD8(+)CD28(−) Regulatory T Cells as a Tool to Treat Autoimmune Disease
title Harnessing CD8(+)CD28(−) Regulatory T Cells as a Tool to Treat Autoimmune Disease
title_full Harnessing CD8(+)CD28(−) Regulatory T Cells as a Tool to Treat Autoimmune Disease
title_fullStr Harnessing CD8(+)CD28(−) Regulatory T Cells as a Tool to Treat Autoimmune Disease
title_full_unstemmed Harnessing CD8(+)CD28(−) Regulatory T Cells as a Tool to Treat Autoimmune Disease
title_short Harnessing CD8(+)CD28(−) Regulatory T Cells as a Tool to Treat Autoimmune Disease
title_sort harnessing cd8(+)cd28(−) regulatory t cells as a tool to treat autoimmune disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616472/
https://www.ncbi.nlm.nih.gov/pubmed/34831195
http://dx.doi.org/10.3390/cells10112973
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