Immunomodulatory Precision: A Narrative Review Exploring the Critical Role of Immune Checkpoint Inhibitors in Cancer Treatment

被引:19
作者
Qiu, Junyu [1 ,2 ]
Cheng, Zilin [1 ,2 ]
Jiang, Zheng [1 ,2 ]
Gan, Luhan [1 ,3 ]
Zhang, Zixuan [1 ,2 ]
Xie, Zhenzhen [1 ]
机构
[1] Nanchang Univ, Coll Basic Med, Nanchang 330006, Peoples R China
[2] Nanchang Univ, Queen Mary Sch, Med Dept, Nanchang 330031, Peoples R China
[3] Nanchang Univ, Huan Kui Sch, Med Dept, Nanchang 330031, Peoples R China
基金
中国国家自然科学基金;
关键词
immune checkpoint inhibitors (ICIs); immune response; combination immunotherapies; cancer treatment; anti-cancer drugs; CELL LUNG-CANCER; TUMOR MUTATIONAL BURDEN; METASTATIC UROTHELIAL CARCINOMA; III RANDOMIZED-TRIAL; T-CELLS; PHASE-III; ACQUIRED-RESISTANCE; PD-1; BLOCKADE; MOLECULAR CHARACTERIZATION; 1ST-LINE TREATMENT;
D O I
10.3390/ijms25105490
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
An immune checkpoint is a signaling pathway that regulates the recognition of antigens by T-cell receptors (TCRs) during an immune response. These checkpoints play a pivotal role in suppressing excessive immune responses and maintaining immune homeostasis against viral or microbial infections. There are several FDA-approved immune checkpoint inhibitors (ICIs), including ipilimumab, pembrolizumab, and avelumab. These ICIs target cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed cell death protein 1 (PD-1), and programmed death ligand 1 (PD-L1). Furthermore, ongoing efforts are focused on developing new ICIs with emerging potential. In comparison to conventional treatments, ICIs offer the advantages of reduced side effects and durable responses. There is growing interest in the potential of combining different ICIs with chemotherapy, radiation therapy, or targeted therapies. This article comprehensively reviews the classification, mechanism of action, application, and combination strategies of ICIs in various cancers and discusses their current limitations. Our objective is to contribute to the future development of more effective anticancer drugs targeting immune checkpoints.
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收藏
页数:32
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