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MDSC in Mice and Men: Mechanisms of Immunosuppression in Cancer

Myeloid-derived suppressor cells (MDSCs) expand during pathological conditions in both humans and mice and their presence is linked to poor clinical outcomes for cancer patients. Studying MDSC immunosuppression is restricted by MDSCs’ rarity, short lifespan, heterogeneity, poor viability after freez...

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Detalles Bibliográficos
Autores principales: Vanhaver, Christophe, van der Bruggen, Pierre, Bruger, Annika M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268873/
https://www.ncbi.nlm.nih.gov/pubmed/34203451
http://dx.doi.org/10.3390/jcm10132872
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author Vanhaver, Christophe
van der Bruggen, Pierre
Bruger, Annika M.
author_facet Vanhaver, Christophe
van der Bruggen, Pierre
Bruger, Annika M.
author_sort Vanhaver, Christophe
collection PubMed
description Myeloid-derived suppressor cells (MDSCs) expand during pathological conditions in both humans and mice and their presence is linked to poor clinical outcomes for cancer patients. Studying MDSC immunosuppression is restricted by MDSCs’ rarity, short lifespan, heterogeneity, poor viability after freezing and the lack of MDSC-specific markers. In this review, we will compare identification and isolation strategies for human and murine MDSCs. We will also assess what direct and indirect immunosuppressive mechanisms have been attributed to MDSCs. While some immunosuppressive mechanisms are well-documented in mice, e.g., generation of ROS, direct evidence is still lacking in humans. In future, bulk or single-cell genomics could elucidate which phenotypic and functional phenotypes MDSCs adopt in particular microenvironments and help to identify potential targets for therapy.
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spelling pubmed-82688732021-07-10 MDSC in Mice and Men: Mechanisms of Immunosuppression in Cancer Vanhaver, Christophe van der Bruggen, Pierre Bruger, Annika M. J Clin Med Review Myeloid-derived suppressor cells (MDSCs) expand during pathological conditions in both humans and mice and their presence is linked to poor clinical outcomes for cancer patients. Studying MDSC immunosuppression is restricted by MDSCs’ rarity, short lifespan, heterogeneity, poor viability after freezing and the lack of MDSC-specific markers. In this review, we will compare identification and isolation strategies for human and murine MDSCs. We will also assess what direct and indirect immunosuppressive mechanisms have been attributed to MDSCs. While some immunosuppressive mechanisms are well-documented in mice, e.g., generation of ROS, direct evidence is still lacking in humans. In future, bulk or single-cell genomics could elucidate which phenotypic and functional phenotypes MDSCs adopt in particular microenvironments and help to identify potential targets for therapy. MDPI 2021-06-28 /pmc/articles/PMC8268873/ /pubmed/34203451 http://dx.doi.org/10.3390/jcm10132872 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
Vanhaver, Christophe
van der Bruggen, Pierre
Bruger, Annika M.
MDSC in Mice and Men: Mechanisms of Immunosuppression in Cancer
title MDSC in Mice and Men: Mechanisms of Immunosuppression in Cancer
title_full MDSC in Mice and Men: Mechanisms of Immunosuppression in Cancer
title_fullStr MDSC in Mice and Men: Mechanisms of Immunosuppression in Cancer
title_full_unstemmed MDSC in Mice and Men: Mechanisms of Immunosuppression in Cancer
title_short MDSC in Mice and Men: Mechanisms of Immunosuppression in Cancer
title_sort mdsc in mice and men: mechanisms of immunosuppression in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268873/
https://www.ncbi.nlm.nih.gov/pubmed/34203451
http://dx.doi.org/10.3390/jcm10132872
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