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Identification of an Immature Subset of PMN-MDSC Correlated to Response to Checkpoint Inhibitor Therapy in Patients with Metastatic Melanoma

SIMPLE SUMMARY: Polymorphonuclear myeloid-derived suppressive cells (PMN-MDSCs) have been associated to bad prognosis and resistance to immune checkpoint inhibitor (ICI) therapy in metastatic melanoma (MM). In this study, we describe an immature subset of PMN-MDSCs capable of a high cytotoxicity aga...

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Autores principales: Gondois-Rey, Françoise, Paul, Magali, Alcaraz, Florence, Bourass, Sarah, Monnier, Jilliana, Malissen, Nausicaa, Grob, Jean-Jacques, Bruger, Annika M., Van Der Bruggen, Pierre, Gaudy-Marqueste, Caroline, Olive, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002694/
https://www.ncbi.nlm.nih.gov/pubmed/33802925
http://dx.doi.org/10.3390/cancers13061362
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author Gondois-Rey, Françoise
Paul, Magali
Alcaraz, Florence
Bourass, Sarah
Monnier, Jilliana
Malissen, Nausicaa
Grob, Jean-Jacques
Bruger, Annika M.
Van Der Bruggen, Pierre
Gaudy-Marqueste, Caroline
Olive, Daniel
author_facet Gondois-Rey, Françoise
Paul, Magali
Alcaraz, Florence
Bourass, Sarah
Monnier, Jilliana
Malissen, Nausicaa
Grob, Jean-Jacques
Bruger, Annika M.
Van Der Bruggen, Pierre
Gaudy-Marqueste, Caroline
Olive, Daniel
author_sort Gondois-Rey, Françoise
collection PubMed
description SIMPLE SUMMARY: Polymorphonuclear myeloid-derived suppressive cells (PMN-MDSCs) have been associated to bad prognosis and resistance to immune checkpoint inhibitor (ICI) therapy in metastatic melanoma (MM). In this study, we describe an immature subset of PMN-MDSCs capable of a high cytotoxicity against T cells mediated by a MAC-1 interaction, characterized by the absence of expression of the signal regulatory protein alpha. This subset is increased in patients responding to ICI therapy. Although the processes involving these cells in vivo are unknown, low-density CD15(+)SIRPα(−) cells might constitute a useful biomarker to monitor clinical response in MM patients. ABSTRACT: PMN-MDSCs support tumor progression and resistance to ICI therapy through their suppressive functions but their heterogeneity limits their use as biomarkers in cancer. Our aim was to investigate the phenotypic and functional subsets of PMN-MDSCs to identify biomarkers of response to ICI therapy. We isolated low-density CD15(+) PMNs from patients with metastatic melanoma and assessed their immune-suppressive capacities. Expression of CD10 and CD16 was used to identify mature and immature subsets and correlate them to inhibition of T cell proliferation or direct cytotoxicity. Frequencies of the PMN-MDSCs subsets were next correlated to the radiological response of 36 patients receiving ICI therapy. Mature activated cells constituted the major population of PMN-MDSCs. They were found in a higher proportion in the pre-treatment blood of patients non responders to ICI. A subset of immature cells characterized by intermediate levels of CD10 and CD16, the absence of expression of SIRPα and a strong direct cytotoxicity to T cells was increased in patients responding to ICI. The paradoxical expansion of such cells during ICI therapy suggests a role of PMNs in the inflammatory events associated to efficient ICI therapy and the usefulness of their monitoring in patients care.
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spelling pubmed-80026942021-03-28 Identification of an Immature Subset of PMN-MDSC Correlated to Response to Checkpoint Inhibitor Therapy in Patients with Metastatic Melanoma Gondois-Rey, Françoise Paul, Magali Alcaraz, Florence Bourass, Sarah Monnier, Jilliana Malissen, Nausicaa Grob, Jean-Jacques Bruger, Annika M. Van Der Bruggen, Pierre Gaudy-Marqueste, Caroline Olive, Daniel Cancers (Basel) Article SIMPLE SUMMARY: Polymorphonuclear myeloid-derived suppressive cells (PMN-MDSCs) have been associated to bad prognosis and resistance to immune checkpoint inhibitor (ICI) therapy in metastatic melanoma (MM). In this study, we describe an immature subset of PMN-MDSCs capable of a high cytotoxicity against T cells mediated by a MAC-1 interaction, characterized by the absence of expression of the signal regulatory protein alpha. This subset is increased in patients responding to ICI therapy. Although the processes involving these cells in vivo are unknown, low-density CD15(+)SIRPα(−) cells might constitute a useful biomarker to monitor clinical response in MM patients. ABSTRACT: PMN-MDSCs support tumor progression and resistance to ICI therapy through their suppressive functions but their heterogeneity limits their use as biomarkers in cancer. Our aim was to investigate the phenotypic and functional subsets of PMN-MDSCs to identify biomarkers of response to ICI therapy. We isolated low-density CD15(+) PMNs from patients with metastatic melanoma and assessed their immune-suppressive capacities. Expression of CD10 and CD16 was used to identify mature and immature subsets and correlate them to inhibition of T cell proliferation or direct cytotoxicity. Frequencies of the PMN-MDSCs subsets were next correlated to the radiological response of 36 patients receiving ICI therapy. Mature activated cells constituted the major population of PMN-MDSCs. They were found in a higher proportion in the pre-treatment blood of patients non responders to ICI. A subset of immature cells characterized by intermediate levels of CD10 and CD16, the absence of expression of SIRPα and a strong direct cytotoxicity to T cells was increased in patients responding to ICI. The paradoxical expansion of such cells during ICI therapy suggests a role of PMNs in the inflammatory events associated to efficient ICI therapy and the usefulness of their monitoring in patients care. MDPI 2021-03-17 /pmc/articles/PMC8002694/ /pubmed/33802925 http://dx.doi.org/10.3390/cancers13061362 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gondois-Rey, Françoise
Paul, Magali
Alcaraz, Florence
Bourass, Sarah
Monnier, Jilliana
Malissen, Nausicaa
Grob, Jean-Jacques
Bruger, Annika M.
Van Der Bruggen, Pierre
Gaudy-Marqueste, Caroline
Olive, Daniel
Identification of an Immature Subset of PMN-MDSC Correlated to Response to Checkpoint Inhibitor Therapy in Patients with Metastatic Melanoma
title Identification of an Immature Subset of PMN-MDSC Correlated to Response to Checkpoint Inhibitor Therapy in Patients with Metastatic Melanoma
title_full Identification of an Immature Subset of PMN-MDSC Correlated to Response to Checkpoint Inhibitor Therapy in Patients with Metastatic Melanoma
title_fullStr Identification of an Immature Subset of PMN-MDSC Correlated to Response to Checkpoint Inhibitor Therapy in Patients with Metastatic Melanoma
title_full_unstemmed Identification of an Immature Subset of PMN-MDSC Correlated to Response to Checkpoint Inhibitor Therapy in Patients with Metastatic Melanoma
title_short Identification of an Immature Subset of PMN-MDSC Correlated to Response to Checkpoint Inhibitor Therapy in Patients with Metastatic Melanoma
title_sort identification of an immature subset of pmn-mdsc correlated to response to checkpoint inhibitor therapy in patients with metastatic melanoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8002694/
https://www.ncbi.nlm.nih.gov/pubmed/33802925
http://dx.doi.org/10.3390/cancers13061362
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