Clinical Perspectives to Overcome Acquired Resistance to Anti-Programmed Death-1 and Anti-Programmed Death Ligand-1 Therapy in Non-Small Cell Lung Cancer

被引:15
|
作者
Lee, Yong Jun [1 ]
Lee, Jii Bum [1 ,2 ]
Ha, Sang-Jun [3 ]
Kim, Hye Ryun [1 ]
机构
[1] Yonsei Univ, Yonsei Canc Ctr, Dept Internal Med, Div Med Oncol,Coll Med, Seoul 03722, South Korea
[2] Yonsei Univ, Wonju Severance Christian Hosp, Div Hematooncol, Coll Med, Wonju 26426, South Korea
[3] Yonsei Univ, Coll Life Sci & Biotechnol, Dept Biochem, Seoul 03722, South Korea
基金
新加坡国家研究基金会;
关键词
acquired resistance; immune checkpoint inhibitors; non-small cell lung cancer; programmed death-1; programmed death ligand-1; IMMUNE CHECKPOINT INHIBITORS; CD8(+) T-CELLS; PD-1; BLOCKADE; TGF-BETA; IFN-GAMMA; IMMUNOTHERAPY; MECHANISMS; ADENOSINE; MACROPHAGES; PROGRESSION;
D O I
10.14348/molcells.2021.0044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Immune checkpoint inhibitors have changed the paradigm of treatment options for non-small cell lung cancer (NSCLC). Monoclonal antibodies targeting programmed death-1 (PD-1) and programmed death ligand-1 (PD-L1) have gained wide attention for their application, which has been shown to result in prolonged survival. Nevertheless, only a limited subset of patients show partial or complete response to PD-1 therapy, and patients who show a response eventually develop resistance to immunotherapy. This article aims to provide an overview of the mechanisms of acquired resistance to anti-PD-1/PD-L1 therapy from the perspective of tumor cells and the surrounding microenvironment. In addition, we address the potential therapeutic targets and ongoing clinical trials, focusing mainly on NSCLC.
引用
收藏
页码:363 / 373
页数:11
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