| Literature DB >> 30287140 |
Jinfang Zhang1, Fabin Dang1, Junming Ren2, Wenyi Wei3.
Abstract
PD-L1, frequently expressed in human cancers, engages with PD-1 on immune cells and contributes to cancer immune evasion. As such, antibodies blocking the PD-1/PD-L1 interaction reactivate cytotoxic T cells to eradicate cancer cells. However, a majority of cancer patients fail to respond to PD-1/PD-L1 blockade with unclear underlying mechanism(s). Recent studies revealed that PD-L1 expression levels on tumor cells might affect the clinical response to anti-PD-1/PD-L1 therapies. Hence, understanding molecular mechanisms for controlling PD-L1 expression will be important to improve the clinical response rate and efficacy of PD-1/PD-L1 blockade. In this review, we primarily focus on summarizing PD-L1 regulation and its potential roles in regulating antitumor immune response, with purpose to optimize anti-PD-1/PD-L1 therapies, benefiting a wider cancer patient population.Entities:
Keywords: Cancer immunotherapy; PD-1/PD-L1; checkpoint blockade; combination therapies; tumor-infiltrating lymphocyte
Mesh:
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Year: 2018 PMID: 30287140 PMCID: PMC6252278 DOI: 10.1016/j.tibs.2018.09.004
Source DB: PubMed Journal: Trends Biochem Sci ISSN: 0968-0004 Impact factor: 13.807