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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8268873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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