TY - JOUR
T1 - Method for the Analysis of the Tumor Microenvironment by Mass Cytometry
T2 - Application to Chronic Lymphocytic Leukemia
AU - Gonder, Susanne
AU - Fernandez Botana, Iria
AU - Wierz, Marina
AU - Pagano, Giulia
AU - Gargiulo, Ernesto
AU - Cosma, Antonio
AU - Moussay, Etienne
AU - Paggetti, Jerome
AU - Largeot, Anne
N1 - Funding Information:
This work was supported by grants from FNRS “Télévie” to SG, IF, MW, GP, and AL (7.4502.19, 7.4529.19, 7.6504.18, 7.4501.18, 7.4502.17, and 7.4503.19), from FNR Luxembourg to EG and JP (PRIDE15/10675146/CANBIO and INTER/DFG/16/11509946) and from Plooschter Projet.
Publisher Copyright:
© Copyright © 2020 Gonder, Fernandez Botana, Wierz, Pagano, Gargiulo, Cosma, Moussay, Paggetti and Largeot.
PY - 2020/10/20
Y1 - 2020/10/20
N2 - 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.
AB - 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.
KW - chronic lymphocytic leukemia
KW - immunosuppression
KW - lymphoma
KW - mass cytometry
KW - microenvironment
UR - http://www.scopus.com/inward/record.url?scp=85095593083&partnerID=8YFLogxK
U2 - 10.3389/fimmu.2020.578176
DO - 10.3389/fimmu.2020.578176
M3 - Review article
C2 - 33193376
AN - SCOPUS:85095593083
SN - 1664-3224
VL - 11
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 578176
ER -