Noncanonical PD-1/PD-L1 Axis in Relation to the Efficacy of Anti-PD Therapy
文献类型:期刊论文
作者 | Long, Yiru3,4; Yu, Xiaolu3,4; Chen, Runqiu2,4; Tong, Yongliang3,4; Gong, Likun1,3,4![]() |
刊名 | FRONTIERS IN IMMUNOLOGY
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出版日期 | 2022-05-18 |
卷号 | 13页码:12 |
关键词 | noncanonical PD-1 PD-L1 axis T-cells tumor cells myeloid cells anti-PD therapy |
ISSN号 | 1664-3224 |
DOI | 10.3389/fimmu.2022.910704 |
通讯作者 | Gong, Likun(lkgong@simm.ac.cn) |
英文摘要 | With programmed death 1/ligand 1 (PD-1/PD-L1) as the cornerstone, anti-PD antibodies have pioneered revolutionary immunotherapies for malignancies. But most patients struggled to respond to anti-PD owing to primary or acquired resistance or even hyperprogression, pointing to more efforts needed to explore this axis. PD-1 constrains T-cell immunoreactivity via engaging with PD-L1 of tumor/myeloid cells is the canonical PD-1/PD-L1 axis function mode. Studies are increasingly aware of the impact of noncanonical PD-1/PD-L1 expression in various cancers. PD-L1 induced on activated T-cells ligates to PD-1 to mediate self-tolerance or acts on intratumoral myeloid cells and other T-cells, affecting their survival, differentiation and immunophenotyping, leading to tumor immunosuppression. Myeloid PD-1 interferes with their proliferation, differentiation, cytokine secretion and phagocytosis, mediating remarkable pro-tumor effects. Tumor cell intrinsic PD-1 signaling has diverse functions in different tumors, resulting in pro-proliferation or proliferation inhibition. These nonclassical PD-1/PD-L1 functions may be novel anti-PD mechanisms or causes of treatment resistance. This review highlights the nonnegligible role of T-cell-intrinsic PD-L1 and tumor/myeloid PD-1 in the cell interplay network and the complex impact on the efficacy of anti-PD antibodies. Reconsidering and rational utilization of the comprehensive PD-1/PD-L1 axis could cumulate breakthroughs in precision treatment and combination for anti-PD therapies. |
WOS关键词 | CD8 T-CELLS ; DEATH LIGAND 1 ; NK CELLS ; DENDRITIC CELLS ; ANTI-PD-L1 ANTIBODY ; M1 PHENOTYPE ; B7 FAMILY ; B7-H1 ; EXPRESSION ; BLOCKADE |
WOS研究方向 | Immunology |
语种 | 英语 |
WOS记录号 | WOS:000805003400001 |
出版者 | FRONTIERS MEDIA SA |
源URL | [http://119.78.100.183/handle/2S10ELR8/301301] ![]() |
专题 | 新药研究国家重点实验室 |
通讯作者 | Gong, Likun |
作者单位 | 1.Chinese Acad Sci, Shanghai Inst Mat Med, Zhongshan Inst Drug Discovery, Zhongshan, Peoples R China 2.Shenyang Pharmaceut Univ, Wuya Coll Innovat, Dept Pharmaceut, Shenyang, Peoples R China 3.Univ Chinese Acad Sci, Beijing, Peoples R China 4.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai, Peoples R China |
推荐引用方式 GB/T 7714 | Long, Yiru,Yu, Xiaolu,Chen, Runqiu,et al. Noncanonical PD-1/PD-L1 Axis in Relation to the Efficacy of Anti-PD Therapy[J]. FRONTIERS IN IMMUNOLOGY,2022,13:12. |
APA | Long, Yiru,Yu, Xiaolu,Chen, Runqiu,Tong, Yongliang,&Gong, Likun.(2022).Noncanonical PD-1/PD-L1 Axis in Relation to the Efficacy of Anti-PD Therapy.FRONTIERS IN IMMUNOLOGY,13,12. |
MLA | Long, Yiru,et al."Noncanonical PD-1/PD-L1 Axis in Relation to the Efficacy of Anti-PD Therapy".FRONTIERS IN IMMUNOLOGY 13(2022):12. |
入库方式: OAI收割
来源:上海药物研究所
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