中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Activating CD8+ T Cells by Pt(IV) Prodrug-Based Nanomedicine and aPD-L1 Antibody for Enhanced Cancer Immunotherapy

文献类型:期刊论文

作者Wang, Bin6,7; Zhou, Jingyu4,5,6; Li, Ruitong3; Tang, Dongsheng6,7; Cao, Zheng2; Xu, Chun1; Xiao, Haihua6,7
刊名ADVANCED MATERIALS
出版日期2024-02-23
页码15
ISSN号0935-9648
关键词chemotherapy immunotherapy immunogenic cell death tumor immune microenvironment
DOI10.1002/adma.202311640
通讯作者Xiao, Haihua(hhxiao@iccas.ac.cn)
英文摘要Recent years have witnessed substantial progress in cancer immunotherapy, specifically T cell-based therapies. However, the application of T cell therapies has been primarily limited to hematologic malignancies, with limited success in the treatment of solid tumors. The main challenge in treating solid tumor is immune escape, which is characterized by reduced antigenicity, diminished immunogenicity, and the development of suppressive tumor immune microenvironments. To address these obstacles and restore T cell-mediated anti-tumor responses, a novel nanoparticle formulation known as PRA@Oxa-c16 is developed. This innovative approach combines retinoic acid and Pt(IV) to specifically target and overcome immune escape. Notably, the therapeutic efficacy of PRA@Oxa-c16 primarily relies on its ability to induce anti-tumor T cell responses, in contrast to the cytotoxicity associated with conventional chemotherapeutic agents. When combined with an immune checkpoint blockade, anti-programmed death-ligand 1 antibody, PRA@Oxa-c16 effectively eliminates solid tumors and induces immune memory responses, which prevent tumor metastasis and recurrence. This promising approach holds great potential for enhancing the treatment of solid tumors with T cell-based immunotherapy.
WOS关键词TRANS-RETINOIC ACID ; THERAPY
资助项目Chinese Academy of Sciences ; National Key Research & Development Program[2022YFC2603900] ; Central Government Guided Local Science and Technology Development Fund (Hebei)[216Z2601G] ; National Natural Science Foundation of China[22175189]
WOS研究方向Chemistry ; Science & Technology - Other Topics ; Materials Science ; Physics
语种英语
出版者WILEY-V C H VERLAG GMBH
WOS记录号WOS:001174635900001
源URL[http://119.78.100.183/handle/2S10ELR8/309904]  
专题中国科学院上海药物研究所
通讯作者Xiao, Haihua
作者单位1.Univ Queensland, Sch Dent, Brisbane, Qld 4006, Australia
2.Univ Calif Los Angeles, Dept Chem & Biomol Engn, Los Angeles, CA 90095 USA
3.Nankai Univ, Coll Chem, Dept Chem, Tianjin 300071, Peoples R China
4.Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
5.Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Mol Med, Hangzhou 310024, Zhejiang, Peoples R China
6.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
7.Chinese Acad Sci, Beijing Natl Lab Mol Sci, Lab Polymer Phys & Chem, Inst Chem, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
Wang, Bin,Zhou, Jingyu,Li, Ruitong,et al. Activating CD8+ T Cells by Pt(IV) Prodrug-Based Nanomedicine and aPD-L1 Antibody for Enhanced Cancer Immunotherapy[J]. ADVANCED MATERIALS,2024:15.
APA Wang, Bin.,Zhou, Jingyu.,Li, Ruitong.,Tang, Dongsheng.,Cao, Zheng.,...&Xiao, Haihua.(2024).Activating CD8+ T Cells by Pt(IV) Prodrug-Based Nanomedicine and aPD-L1 Antibody for Enhanced Cancer Immunotherapy.ADVANCED MATERIALS,15.
MLA Wang, Bin,et al."Activating CD8+ T Cells by Pt(IV) Prodrug-Based Nanomedicine and aPD-L1 Antibody for Enhanced Cancer Immunotherapy".ADVANCED MATERIALS (2024):15.

入库方式: OAI收割

来源:上海药物研究所

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