PD-1 and PD-L1 in cancer immunotherapy: clinical implications and future considerations

Programmed death-1 (PD-1) is a cell surface receptor that functions as a T cell checkpoint and plays a central role in regulating T cell exhaustion. Binding of PD-1 to its ligand, programmed death-ligand 1 (PD-L1), activates downstream signaling pathways and inhibits T cell activation. Moreover abno...

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Published inHuman vaccines & immunotherapeutics Vol. 15; no. 5; pp. 1111 - 1122
Main Authors Jiang, Yongshuai, Chen, Ming, Nie, Hong, Yuan, Yuanyang
Format Journal Article
LanguageEnglish
Published United States Taylor & Francis 04.05.2019
Taylor & Francis Group
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Summary:Programmed death-1 (PD-1) is a cell surface receptor that functions as a T cell checkpoint and plays a central role in regulating T cell exhaustion. Binding of PD-1 to its ligand, programmed death-ligand 1 (PD-L1), activates downstream signaling pathways and inhibits T cell activation. Moreover abnormally high PD-L1 expression on tumor cells and antigen-presenting cells in the tumor microenvironment mediates tumor immune escape, and the development of anti-PD-1/PD-L1 antibodies has recently become a hot topic in cancer immunotherapy. Here, we review the structure of PD-1 and PD-L1, the function of the PD-1/PD-L1 signaling pathway, the application of PD-1 or PD-L1 monoclonal antibodies and future directions for anti-PD-1/PD-L1 antibodies with combination therapies. Cancer immunotherapy using PD-1/PD-L1 immune checkpoint blockade may require more studies, and this approach may be curative for patients with many types of cancer in the future.
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Color versions of one or more of the figures in the article can be found online at www.tandfonline.com/khvi.
These two authors contributed equally to this paper.
ISSN:2164-5515
2164-554X
2164-554X
DOI:10.1080/21645515.2019.1571892