中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Engineered nanomedicines block the PD-1/PD-L1 axis for potentiated cancer immunotherapy

文献类型:期刊论文

作者Li, Jun-hao3,4,5; Huang, Lu-jia2,3,4; Zhou, Hui-ling3,4; Shan, Yi-ming2,3,4; Chen, Fang-min2,3,4; Lehto, Vesa-Pekka1; Xu, Wu-jun1; Luo, Li-qiang5; Yu, Hai-jun2,3,4
刊名ACTA PHARMACOLOGICA SINICA
出版日期2022-04-28
页码10
关键词cancer immunotherapy immune checkpoint blockade PD-1/PD-L1 axis nanomedicine nanosized drug delivery systems
ISSN号1671-4083
DOI10.1038/s41401-022-00910-w
通讯作者Huang, Lu-jia(huanglujia@simm.ac.cn) ; Xu, Wu-jun(wujun.xu@uef.fi) ; Yu, Hai-jun(hjyu@simm.ac.cn)
英文摘要Immunotherapy, in particular immune checkpoint blockade (ICB) therapy targeting the programmed cell death-1 (PD-1)/programmed cell death ligand-1 (PD-L1) axis, has remarkably revolutionized cancer treatment in the clinic. Anti-PD-1/PD-L1 therapy is designed to restore the antitumor response of cytotoxic T cells (CTLs) by blocking the interaction between PD-L1 on tumour cells and PD-1 on CTLs. Nevertheless, current anti-PD-1/PD-L1 therapy suffers from poor therapeutic outcomes in a large variety of solid tumours due to insufficient tumour specificity, severe cytotoxic effects, and the occurrence of immune resistance. In recent years, nanosized drug delivery systems (NDDSs), endowed with highly efficient tumour targeting and versatility for combination therapy, have paved a new avenue for cancer immunotherapy. In this review article, we summarized the recent advances in NDDSs for anti-PD-1/PD-L1 therapy. We then discussed the challenges and further provided perspectives to promote the clinical application of NDDS-based anti-PD-1/PD-L1 therapy.
WOS关键词IMMUNE CHECKPOINT BLOCKADE ; ANTITUMOR IMMUNITY ; PD-1 BLOCKADE ; NIVOLUMAB ; IPILIMUMAB ; RESISTANCE ; ANTI-PD-1 ; PEMBROLIZUMAB ; METASTASIS ; ANTIBODIES
资助项目National Natural Science Foundation of China[51873228] ; National Natural Science Foundation of China[32050410287] ; International Cooperation Project of Science and Technology Commission of Shanghai Municipality[20430711800]
WOS研究方向Chemistry ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000788463900001
出版者NATURE PUBL GROUP
源URL[http://119.78.100.183/handle/2S10ELR8/300983]  
专题新药研究国家重点实验室
通讯作者Huang, Lu-jia; Xu, Wu-jun; Yu, Hai-jun
作者单位1.Univ Eastern Finland, Dept Appl Phys, Kuopio 70211, Finland
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Chinese Acad Sci, Shanghai Inst Mat Med, Ctr Pharmaceut, Shanghai 201203, Peoples R China
4.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
5.Shanghai Univ, Coll Sci, Shanghai 200444, Peoples R China
推荐引用方式
GB/T 7714
Li, Jun-hao,Huang, Lu-jia,Zhou, Hui-ling,et al. Engineered nanomedicines block the PD-1/PD-L1 axis for potentiated cancer immunotherapy[J]. ACTA PHARMACOLOGICA SINICA,2022:10.
APA Li, Jun-hao.,Huang, Lu-jia.,Zhou, Hui-ling.,Shan, Yi-ming.,Chen, Fang-min.,...&Yu, Hai-jun.(2022).Engineered nanomedicines block the PD-1/PD-L1 axis for potentiated cancer immunotherapy.ACTA PHARMACOLOGICA SINICA,10.
MLA Li, Jun-hao,et al."Engineered nanomedicines block the PD-1/PD-L1 axis for potentiated cancer immunotherapy".ACTA PHARMACOLOGICA SINICA (2022):10.

入库方式: OAI收割

来源:上海药物研究所

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