Myeloid-Derived Suppressor Cells and Radiotherapy

Author:

Jiménez-Cortegana Carlos12ORCID,Galassi Claudia1,Klapp Vanessa1,Gabrilovich Dmitry I.3,Galluzzi Lorenzo145

Affiliation:

1. 1Department of Radiation Oncology, Weill Cornell Medical College, New York, New York.

2. 2Department of Medical Biochemistry, Molecular Biology and Immunology, Faculty of Medicine, University of Seville, Seville, Spain.

3. 3Immuno-Oncology, AstraZeneca, Gaithersburg, Maryland.

4. 4Sandra and Edward Meyer Cancer Center, New York, New York.

5. 5Caryl and Israel Englander Institute for Precision Medicine, New York, New York.

Abstract

AbstractMyeloid-derived suppressor cells (MDSC) are a heterogeneous population of pathologically activated, mostly immature, myeloid cells that exert robust immunosuppressive functions. MDSCs expand during oncogenesis and have been linked to accelerated disease progression and resistance to treatment in both preclinical tumor models and patients with cancer. Thus, MDSCs stand out as promising targets for the development of novel immunotherapeutic regimens with superior efficacy. Here, we summarize accumulating preclinical and clinical evidence indicating that MDSCs also hamper the efficacy of radiotherapy (RT), as we critically discuss the potential of MDSC-targeting strategies as tools to achieve superior immunotherapeutic tumor control by RT in the clinic.

Funder

US DoD BRCP

2019 Laura Ziskin Prize in Translational Research

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Immunology

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