Mechanisms underlying low-clinical responses to PD-1/PD-L1 blocking antibodies in immunotherapy of cancer: a key role of exosomal PD-L1

• Published in: Journal for immunotherapy of cancer Vol. 9; no. 1; p. e001698
• Main Authors: Yin, Zi, Yu, Min, Ma, Tingting, Zhang, Chuanzhao, Huang, Shanzhou, Karimzadeh, Mohammad Reza, Momtazi-Borojeni, Amir Abaas, Chen, Sheng
• Format: Journal Article
• Language: English
• Published: England BMJ Publishing Group Ltd 01.01.2021; BMJ Publishing Group LTD; BMJ Publishing Group
• Subjects: Antigens; Apoptosis; B7-H1 Antigen - drug effects; B7-H1 Antigen - metabolism; Bladder cancer; Breast cancer; Cancer; Cell death; Colorectal cancer; Cytokines; Cytotoxicity; Disease Progression; Drug Resistance, Neoplasm; Exosomes - drug effects; Exosomes - metabolism; Extracellular vesicles; FDA approval; Gene Expression Regulation, Neoplastic - drug effects; Head & neck cancer; Humans; Immune Checkpoint Inhibitors - pharmacology; Immune Checkpoint Inhibitors - therapeutic use; Immunotherapy; Kidney cancer; Kinases; Ligands; Liver cancer; Lung cancer; Lymphocytes; Melanoma; Metastasis; Monoclonal antibodies; Mutation; Neoplasms - drug therapy; Neoplasms - immunology; Peptides; programmed cell death 1 receptor; Programmed Cell Death 1 Receptor - drug effects; Programmed Cell Death 1 Receptor - metabolism; Response rates; Review; T cell receptors; Transcription factors; tumor escape; Tumors; Up-Regulation - drug effects; United States > US; programmed cell death 1 receptor; tumor escape; immunotherapy
• ISSN: 2051-1426; 2051-1426
• DOI: 10.1136/jitc-2020-001698

Exosomes, as the main group of extracellular vesicles, are biologically active lipid-bilayer vesicles that are naturally released from different types of normal or tumor cells. These vesicles play an important role in intercellular communication and influence the extracellular environment and the immune system. Emerging evidence demonstrates that cancer-derived exosomes are enriched in immunosuppressive proteins, such as the programmed death-ligand 1 (PD-L1). PD-L1 and its receptor programmed cell death protein 1 (PD-1) are the key immune checkpoint molecules that promote tumor progression via negative regulation of immune responses. PDL-1 is highly expressed on the surface of tumor cells and binds to PD-1 on the surface of activated T cells, leading to suppression of T cells, which consequently enables cancer cells to escape antitumor immunity. Currently, there are several Food and Drug Administration-approved monoclonal antibodies blocking PD-1/PD-L1 interaction, which are clinically used for cancer treatment. However, despite impressive treatment outcomes, some patients show poor response to PD-1/PD-L1 blockade. Of note, tumor-derived exosomes containing PD-L1 can recapitulate the effect of cell-surface PD-L1. There is evidence that reveals a significant association between levels of circulating exosomal PD-L1 and rate of response to anti-PD-1/PD-L1 antibody therapy. The present article reviews the role of exosomal PDL-1 in the therapeutic resistance to anti-PD-1/PD-L1 treatment. Importantly, it is suggested that the removal of exosomal PDL-1 could serve as a therapeutic adjuvant for enhancing the efficacy of anti-PD-1/PD-L1 therapy in patients with cancer.