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VISTA: A Mediator of Quiescence and a Promising Target in Cancer Immunotherapy

V-domain Ig suppressor of T cell activation (VISTA) is a B7 family member that maintains T cell and myeloid quiescence and is a promising target for combination cancer immunotherapy. During inflammatory challenges, VISTA activity reprograms macrophages towards reduced production of proinflammatory c...

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Detalles Bibliográficos
Autores principales: Yuan, Long, Tatineni, Jahnavi, Mahoney, Kathleen M., Freeman, Gordon J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088836/
https://www.ncbi.nlm.nih.gov/pubmed/33495077
http://dx.doi.org/10.1016/j.it.2020.12.008
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author Yuan, Long
Tatineni, Jahnavi
Mahoney, Kathleen M.
Freeman, Gordon J.
author_facet Yuan, Long
Tatineni, Jahnavi
Mahoney, Kathleen M.
Freeman, Gordon J.
author_sort Yuan, Long
collection PubMed
description V-domain Ig suppressor of T cell activation (VISTA) is a B7 family member that maintains T cell and myeloid quiescence and is a promising target for combination cancer immunotherapy. During inflammatory challenges, VISTA activity reprograms macrophages towards reduced production of proinflammatory cytokines and increased production of interleukin (IL)-10 and other anti-inflammatory mediators. The interaction of VISTA with its ligands is regulated by pH, and the acidic pH ~6.0 in the tumor microenvironment (TME) facilitates VISTA binding to P-selectin glycoprotein ligand 1 (PSGL-1). Targeting intratumoral pH might be a way to reduce the immunoinhibitory activity of the VISTA pathway and enhance antitumor immune responses. We review differences among VISTA therapeutics under development as candidate immunotherapies, focusing on VISTA binding partners and the unique structural features of this interaction.
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spelling pubmed-80888362021-05-02 VISTA: A Mediator of Quiescence and a Promising Target in Cancer Immunotherapy Yuan, Long Tatineni, Jahnavi Mahoney, Kathleen M. Freeman, Gordon J. Trends Immunol Article V-domain Ig suppressor of T cell activation (VISTA) is a B7 family member that maintains T cell and myeloid quiescence and is a promising target for combination cancer immunotherapy. During inflammatory challenges, VISTA activity reprograms macrophages towards reduced production of proinflammatory cytokines and increased production of interleukin (IL)-10 and other anti-inflammatory mediators. The interaction of VISTA with its ligands is regulated by pH, and the acidic pH ~6.0 in the tumor microenvironment (TME) facilitates VISTA binding to P-selectin glycoprotein ligand 1 (PSGL-1). Targeting intratumoral pH might be a way to reduce the immunoinhibitory activity of the VISTA pathway and enhance antitumor immune responses. We review differences among VISTA therapeutics under development as candidate immunotherapies, focusing on VISTA binding partners and the unique structural features of this interaction. 2021-01-23 2021-03 /pmc/articles/PMC8088836/ /pubmed/33495077 http://dx.doi.org/10.1016/j.it.2020.12.008 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Yuan, Long
Tatineni, Jahnavi
Mahoney, Kathleen M.
Freeman, Gordon J.
VISTA: A Mediator of Quiescence and a Promising Target in Cancer Immunotherapy
title VISTA: A Mediator of Quiescence and a Promising Target in Cancer Immunotherapy
title_full VISTA: A Mediator of Quiescence and a Promising Target in Cancer Immunotherapy
title_fullStr VISTA: A Mediator of Quiescence and a Promising Target in Cancer Immunotherapy
title_full_unstemmed VISTA: A Mediator of Quiescence and a Promising Target in Cancer Immunotherapy
title_short VISTA: A Mediator of Quiescence and a Promising Target in Cancer Immunotherapy
title_sort vista: a mediator of quiescence and a promising target in cancer immunotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088836/
https://www.ncbi.nlm.nih.gov/pubmed/33495077
http://dx.doi.org/10.1016/j.it.2020.12.008
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