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CCR3 plays a role in murine age-related cognitive changes and T-cell infiltration into the brain

Targeting immune-mediated, age-related, biology has the potential to be a transformative therapeutic strategy. However, the redundant nature of the multiple cytokines that change with aging requires identification of a master downstream regulator to successfully exert therapeutic efficacy. Here, we...

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Autores principales: Rege, Sanket V., Teichert, Arnaud, Masumi, Juliet, Dhande, Onkar S., Harish, Reema, Higgins, Brett W., Lopez, Yesenia, Akrapongpisak, Lily, Hackbart, Hannah, Caryotakis, Sofia, Leone, Dino P., Szoke, Balazs, Hannestad, Jonas, Nikolich, Karoly, Braithwaite, Steven P., Minami, S. Sakura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10024715/
https://www.ncbi.nlm.nih.gov/pubmed/36934154
http://dx.doi.org/10.1038/s42003-023-04665-w
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author Rege, Sanket V.
Teichert, Arnaud
Masumi, Juliet
Dhande, Onkar S.
Harish, Reema
Higgins, Brett W.
Lopez, Yesenia
Akrapongpisak, Lily
Hackbart, Hannah
Caryotakis, Sofia
Leone, Dino P.
Szoke, Balazs
Hannestad, Jonas
Nikolich, Karoly
Braithwaite, Steven P.
Minami, S. Sakura
author_facet Rege, Sanket V.
Teichert, Arnaud
Masumi, Juliet
Dhande, Onkar S.
Harish, Reema
Higgins, Brett W.
Lopez, Yesenia
Akrapongpisak, Lily
Hackbart, Hannah
Caryotakis, Sofia
Leone, Dino P.
Szoke, Balazs
Hannestad, Jonas
Nikolich, Karoly
Braithwaite, Steven P.
Minami, S. Sakura
author_sort Rege, Sanket V.
collection PubMed
description Targeting immune-mediated, age-related, biology has the potential to be a transformative therapeutic strategy. However, the redundant nature of the multiple cytokines that change with aging requires identification of a master downstream regulator to successfully exert therapeutic efficacy. Here, we discovered CCR3 as a prime candidate, and inhibition of CCR3 has pro-cognitive benefits in mice, but these benefits are not driven by an obvious direct action on central nervous system (CNS)-resident cells. Instead, CCR3-expressing T cells in the periphery that are modulated in aging inhibit infiltration of these T cells across the blood-brain barrier and reduce neuroinflammation. The axis of CCR3-expressing T cells influencing crosstalk from periphery to brain provides a therapeutically tractable link. These findings indicate the broad therapeutic potential of CCR3 inhibition in a spectrum of neuroinflammatory diseases of aging.
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spelling pubmed-100247152023-03-20 CCR3 plays a role in murine age-related cognitive changes and T-cell infiltration into the brain Rege, Sanket V. Teichert, Arnaud Masumi, Juliet Dhande, Onkar S. Harish, Reema Higgins, Brett W. Lopez, Yesenia Akrapongpisak, Lily Hackbart, Hannah Caryotakis, Sofia Leone, Dino P. Szoke, Balazs Hannestad, Jonas Nikolich, Karoly Braithwaite, Steven P. Minami, S. Sakura Commun Biol Article Targeting immune-mediated, age-related, biology has the potential to be a transformative therapeutic strategy. However, the redundant nature of the multiple cytokines that change with aging requires identification of a master downstream regulator to successfully exert therapeutic efficacy. Here, we discovered CCR3 as a prime candidate, and inhibition of CCR3 has pro-cognitive benefits in mice, but these benefits are not driven by an obvious direct action on central nervous system (CNS)-resident cells. Instead, CCR3-expressing T cells in the periphery that are modulated in aging inhibit infiltration of these T cells across the blood-brain barrier and reduce neuroinflammation. The axis of CCR3-expressing T cells influencing crosstalk from periphery to brain provides a therapeutically tractable link. These findings indicate the broad therapeutic potential of CCR3 inhibition in a spectrum of neuroinflammatory diseases of aging. Nature Publishing Group UK 2023-03-18 /pmc/articles/PMC10024715/ /pubmed/36934154 http://dx.doi.org/10.1038/s42003-023-04665-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Rege, Sanket V.
Teichert, Arnaud
Masumi, Juliet
Dhande, Onkar S.
Harish, Reema
Higgins, Brett W.
Lopez, Yesenia
Akrapongpisak, Lily
Hackbart, Hannah
Caryotakis, Sofia
Leone, Dino P.
Szoke, Balazs
Hannestad, Jonas
Nikolich, Karoly
Braithwaite, Steven P.
Minami, S. Sakura
CCR3 plays a role in murine age-related cognitive changes and T-cell infiltration into the brain
title CCR3 plays a role in murine age-related cognitive changes and T-cell infiltration into the brain
title_full CCR3 plays a role in murine age-related cognitive changes and T-cell infiltration into the brain
title_fullStr CCR3 plays a role in murine age-related cognitive changes and T-cell infiltration into the brain
title_full_unstemmed CCR3 plays a role in murine age-related cognitive changes and T-cell infiltration into the brain
title_short CCR3 plays a role in murine age-related cognitive changes and T-cell infiltration into the brain
title_sort ccr3 plays a role in murine age-related cognitive changes and t-cell infiltration into the brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10024715/
https://www.ncbi.nlm.nih.gov/pubmed/36934154
http://dx.doi.org/10.1038/s42003-023-04665-w
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