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Regulatory T-cell therapy approaches

Regulatory T cells (Tregs) have enormous therapeutic potential to treat a variety of immunopathologies characterized by aberrant immune activation. Adoptive transfer of ex vivo expanded autologous Tregs continues to progress through mid- to late-phase clinical trials in several disease spaces and ha...

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Detalles Bibliográficos
Autores principales: McCallion, Oliver, Bilici, Merve, Hester, Joanna, Issa, Fadi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019137/
https://www.ncbi.nlm.nih.gov/pubmed/35960852
http://dx.doi.org/10.1093/cei/uxac078
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author McCallion, Oliver
Bilici, Merve
Hester, Joanna
Issa, Fadi
author_facet McCallion, Oliver
Bilici, Merve
Hester, Joanna
Issa, Fadi
author_sort McCallion, Oliver
collection PubMed
description Regulatory T cells (Tregs) have enormous therapeutic potential to treat a variety of immunopathologies characterized by aberrant immune activation. Adoptive transfer of ex vivo expanded autologous Tregs continues to progress through mid- to late-phase clinical trials in several disease spaces and has generated promising preliminary safety and efficacy signals to date. However, the practicalities of this strategy outside of the clinical trial setting remain challenging. Here, we review the current landscape of regulatory T-cell therapy, considering emergent approaches and technologies presenting novel ways to engage Tregs, and reflect on the progress necessary to deliver their therapeutic potential to patients.
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spelling pubmed-100191372023-03-17 Regulatory T-cell therapy approaches McCallion, Oliver Bilici, Merve Hester, Joanna Issa, Fadi Clin Exp Immunol Review Series: Therapeutic opportunities for regulatory T cell enhancing approaches (Series Editors: David F. Tough & Giovanna Lombardi) Regulatory T cells (Tregs) have enormous therapeutic potential to treat a variety of immunopathologies characterized by aberrant immune activation. Adoptive transfer of ex vivo expanded autologous Tregs continues to progress through mid- to late-phase clinical trials in several disease spaces and has generated promising preliminary safety and efficacy signals to date. However, the practicalities of this strategy outside of the clinical trial setting remain challenging. Here, we review the current landscape of regulatory T-cell therapy, considering emergent approaches and technologies presenting novel ways to engage Tregs, and reflect on the progress necessary to deliver their therapeutic potential to patients. Oxford University Press 2022-08-12 /pmc/articles/PMC10019137/ /pubmed/35960852 http://dx.doi.org/10.1093/cei/uxac078 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Immunology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Series: Therapeutic opportunities for regulatory T cell enhancing approaches (Series Editors: David F. Tough & Giovanna Lombardi)
McCallion, Oliver
Bilici, Merve
Hester, Joanna
Issa, Fadi
Regulatory T-cell therapy approaches
title Regulatory T-cell therapy approaches
title_full Regulatory T-cell therapy approaches
title_fullStr Regulatory T-cell therapy approaches
title_full_unstemmed Regulatory T-cell therapy approaches
title_short Regulatory T-cell therapy approaches
title_sort regulatory t-cell therapy approaches
topic Review Series: Therapeutic opportunities for regulatory T cell enhancing approaches (Series Editors: David F. Tough & Giovanna Lombardi)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019137/
https://www.ncbi.nlm.nih.gov/pubmed/35960852
http://dx.doi.org/10.1093/cei/uxac078
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