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The Generation and Identity of Human Myeloid-Derived Suppressor Cells

Myeloid-derived suppressor cells (MDSCs) are cells of myeloid lineage with a potent immunosuppressive capacity. They are present in cancer patients as well as in patients with severe inflammatory conditions and infections. MDSCs exist as two main subtypes, the granulocytic (G-MDSCs) and the monocyti...

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Detalles Bibliográficos
Autores principales: Bergenfelz, Caroline, Leandersson, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025543/
https://www.ncbi.nlm.nih.gov/pubmed/32117758
http://dx.doi.org/10.3389/fonc.2020.00109
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author Bergenfelz, Caroline
Leandersson, Karin
author_facet Bergenfelz, Caroline
Leandersson, Karin
author_sort Bergenfelz, Caroline
collection PubMed
description Myeloid-derived suppressor cells (MDSCs) are cells of myeloid lineage with a potent immunosuppressive capacity. They are present in cancer patients as well as in patients with severe inflammatory conditions and infections. MDSCs exist as two main subtypes, the granulocytic (G-MDSCs) and the monocytic (Mo-MDSCs) type, as defined by their surface phenotype and functions. While the functions of MDSCs have been investigated in depth, the origin of human MDSCs is less characterized and even controversial. In this review, we recapitulate theories on how MDSCs are generated in mice, and whether this knowledge is translatable into human MDSC biology, as well as on problems of defining MDSCs by their immature cell surface phenotype in relation to the plasticity of myeloid cells. Finally, the challenge of pharmacological targeting of MDSCs in the future is envisioned.
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spelling pubmed-70255432020-02-28 The Generation and Identity of Human Myeloid-Derived Suppressor Cells Bergenfelz, Caroline Leandersson, Karin Front Oncol Oncology Myeloid-derived suppressor cells (MDSCs) are cells of myeloid lineage with a potent immunosuppressive capacity. They are present in cancer patients as well as in patients with severe inflammatory conditions and infections. MDSCs exist as two main subtypes, the granulocytic (G-MDSCs) and the monocytic (Mo-MDSCs) type, as defined by their surface phenotype and functions. While the functions of MDSCs have been investigated in depth, the origin of human MDSCs is less characterized and even controversial. In this review, we recapitulate theories on how MDSCs are generated in mice, and whether this knowledge is translatable into human MDSC biology, as well as on problems of defining MDSCs by their immature cell surface phenotype in relation to the plasticity of myeloid cells. Finally, the challenge of pharmacological targeting of MDSCs in the future is envisioned. Frontiers Media S.A. 2020-02-07 /pmc/articles/PMC7025543/ /pubmed/32117758 http://dx.doi.org/10.3389/fonc.2020.00109 Text en Copyright © 2020 Bergenfelz and Leandersson. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Bergenfelz, Caroline
Leandersson, Karin
The Generation and Identity of Human Myeloid-Derived Suppressor Cells
title The Generation and Identity of Human Myeloid-Derived Suppressor Cells
title_full The Generation and Identity of Human Myeloid-Derived Suppressor Cells
title_fullStr The Generation and Identity of Human Myeloid-Derived Suppressor Cells
title_full_unstemmed The Generation and Identity of Human Myeloid-Derived Suppressor Cells
title_short The Generation and Identity of Human Myeloid-Derived Suppressor Cells
title_sort generation and identity of human myeloid-derived suppressor cells
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025543/
https://www.ncbi.nlm.nih.gov/pubmed/32117758
http://dx.doi.org/10.3389/fonc.2020.00109
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