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Method for the Analysis of the Tumor Microenvironment by Mass Cytometry: Application to Chronic Lymphocytic Leukemia

In the past 20 years, the interest for the tumor microenvironment (TME) has exponentially increased. Indeed, it is now commonly admitted that the TME plays a crucial role in cancer development, maintenance, immune escape and resistance to therapy. This stands true for hematological malignancies as w...

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Autores principales: Gonder, Susanne, Fernandez Botana, Iria, Wierz, Marina, Pagano, Giulia, Gargiulo, Ernesto, Cosma, Antonio, Moussay, Etienne, Paggetti, Jerome, Largeot, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606286/
https://www.ncbi.nlm.nih.gov/pubmed/33193376
http://dx.doi.org/10.3389/fimmu.2020.578176
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author Gonder, Susanne
Fernandez Botana, Iria
Wierz, Marina
Pagano, Giulia
Gargiulo, Ernesto
Cosma, Antonio
Moussay, Etienne
Paggetti, Jerome
Largeot, Anne
author_facet Gonder, Susanne
Fernandez Botana, Iria
Wierz, Marina
Pagano, Giulia
Gargiulo, Ernesto
Cosma, Antonio
Moussay, Etienne
Paggetti, Jerome
Largeot, Anne
author_sort Gonder, Susanne
collection PubMed
description In the past 20 years, the interest for the tumor microenvironment (TME) has exponentially increased. Indeed, it is now commonly admitted that the TME plays a crucial role in cancer development, maintenance, immune escape and resistance to therapy. This stands true for hematological malignancies as well. A considerable amount of newly developed therapies are directed against the cancer-supporting TME instead of targeting tumor cells themselves. However, the TME is often not clearly defined. In addition, the unique phenotype of each tumor and the variability among patients limit the success of such therapies. Recently, our group took advantage of the mass cytometry technology to unveil the specific TME in the context of chronic lymphocytic leukemia (CLL) in mice. We found the enrichment of LAG3 and PD1, two immune checkpoints. We tested an antibody-based immunotherapy, targeting these two molecules. This combination of antibodies was successful in the treatment of murine CLL. In this methods article, we provide a detailed protocol for the staining of CLL TME cells aiming at their characterization using mass cytometry. We include panel design and validation, sample preparation and acquisition, machine set-up, quality control, and analysis. Additionally, we discuss different advantages and pitfalls of this technique.
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spelling pubmed-76062862020-11-13 Method for the Analysis of the Tumor Microenvironment by Mass Cytometry: Application to Chronic Lymphocytic Leukemia Gonder, Susanne Fernandez Botana, Iria Wierz, Marina Pagano, Giulia Gargiulo, Ernesto Cosma, Antonio Moussay, Etienne Paggetti, Jerome Largeot, Anne Front Immunol Immunology In the past 20 years, the interest for the tumor microenvironment (TME) has exponentially increased. Indeed, it is now commonly admitted that the TME plays a crucial role in cancer development, maintenance, immune escape and resistance to therapy. This stands true for hematological malignancies as well. A considerable amount of newly developed therapies are directed against the cancer-supporting TME instead of targeting tumor cells themselves. However, the TME is often not clearly defined. In addition, the unique phenotype of each tumor and the variability among patients limit the success of such therapies. Recently, our group took advantage of the mass cytometry technology to unveil the specific TME in the context of chronic lymphocytic leukemia (CLL) in mice. We found the enrichment of LAG3 and PD1, two immune checkpoints. We tested an antibody-based immunotherapy, targeting these two molecules. This combination of antibodies was successful in the treatment of murine CLL. In this methods article, we provide a detailed protocol for the staining of CLL TME cells aiming at their characterization using mass cytometry. We include panel design and validation, sample preparation and acquisition, machine set-up, quality control, and analysis. Additionally, we discuss different advantages and pitfalls of this technique. Frontiers Media S.A. 2020-10-20 /pmc/articles/PMC7606286/ /pubmed/33193376 http://dx.doi.org/10.3389/fimmu.2020.578176 Text en Copyright © 2020 Gonder, Fernandez Botana, Wierz, Pagano, Gargiulo, Cosma, Moussay, Paggetti and Largeot 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 Immunology
Gonder, Susanne
Fernandez Botana, Iria
Wierz, Marina
Pagano, Giulia
Gargiulo, Ernesto
Cosma, Antonio
Moussay, Etienne
Paggetti, Jerome
Largeot, Anne
Method for the Analysis of the Tumor Microenvironment by Mass Cytometry: Application to Chronic Lymphocytic Leukemia
title Method for the Analysis of the Tumor Microenvironment by Mass Cytometry: Application to Chronic Lymphocytic Leukemia
title_full Method for the Analysis of the Tumor Microenvironment by Mass Cytometry: Application to Chronic Lymphocytic Leukemia
title_fullStr Method for the Analysis of the Tumor Microenvironment by Mass Cytometry: Application to Chronic Lymphocytic Leukemia
title_full_unstemmed Method for the Analysis of the Tumor Microenvironment by Mass Cytometry: Application to Chronic Lymphocytic Leukemia
title_short Method for the Analysis of the Tumor Microenvironment by Mass Cytometry: Application to Chronic Lymphocytic Leukemia
title_sort method for the analysis of the tumor microenvironment by mass cytometry: application to chronic lymphocytic leukemia
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606286/
https://www.ncbi.nlm.nih.gov/pubmed/33193376
http://dx.doi.org/10.3389/fimmu.2020.578176
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