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Tumor Microenvironment-Activatable Prodrug Vesicles for Nanoenabled Cancer Chemoimmunotherapy Combining Immunogenic Cell Death Induction and CD47 Blockade
文献类型:期刊论文
作者 | Zhou, Fangyuan2,3,4; Feng, Bing1,2,3; Yu, Haijun2,3![]() ![]() |
刊名 | ADVANCED MATERIALS
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出版日期 | 2019-04-05 |
卷号 | 31期号:14页码:11 |
关键词 | cancer immunotherapy CD47 blockade immunogenic cell death prodrug vesicles tumor microenvironment |
ISSN号 | 0935-9648 |
DOI | 10.1002/adma.201805888 |
通讯作者 | Yu, Haijun(hjyu@simm.ac.cn) ; Li, Yaping(ypli@simm.ac.cn) |
英文摘要 | Chemoimmunotherapy is reported to activate a robust T cell antitumor immune response by triggering immunogenic cell death (ICD), which has initiated a number of clinical trials. However, current chemoimmunotherapy is restricted to a small fraction of patients due to low drug delivery efficacy and immunosuppression within the tumor microenvironment. A tumor microenvironment-activatable prodrug vesicle for cancer chemoimmunotherapy using ICD is herein reported. The prodrug vesicles are engineered by integrating an oxaliplatin (OXA) prodrug and PEGylated photosensitizer (PS) into a single nanoplatform, which show tumor-specific accumulation, activation, and deep penetration in response to the tumoral acidic and enzymatic microenvironment. It is demonstrated that codelivery of OXA prodrug and PS can trigger ICD of the tumor cells by immunogenic cells killing. The combination of prodrug vesicle-induced ICD with (I) over cap +/- CD47-mediated CD47 blockade further facilitates dendritic cell (DC) maturation, promotes antigen presentation by DCs, and eventually propagates the antitumor immunity of ICD. CD47 blockade and ICD induction efficiently inhibit the growth of both primary and abscopal tumors, suppress tumor metastasis, and prevent tumor recurrence. Collectively, these results imply that boosting antitumor immunity using ICD induction and suppressing tumor immune evasion via CD47 blockade might be promising for improved cancer chemoimmunotherapy. |
WOS关键词 | THERAPY ; IMMUNOTHERAPY ; CHEMOTHERAPY ; SURVIVAL ; TARGET |
资助项目 | National Natural Science Foundation of China[31671024] ; National Natural Science Foundation of China[31622025] ; National Natural Science Foundation of China[51873228] ; National Natural Science Foundation of China[81521005] ; National Natural Science Foundation of China[81722037] ; Strategic Priority Research Program of CAS[XDA12050307] ; Natural Science Foundation of Jiangsu Province[BK20170006] ; Natural Science Foundation of Jiangsu Province[BK20160379] |
WOS研究方向 | Chemistry ; Science & Technology - Other Topics ; Materials Science ; Physics |
语种 | 英语 |
WOS记录号 | WOS:000467974100001 |
出版者 | WILEY-V C H VERLAG GMBH |
源URL | [http://119.78.100.183/handle/2S10ELR8/289823] ![]() |
专题 | 新药研究国家重点实验室 |
通讯作者 | Yu, Haijun; Li, Yaping |
作者单位 | 1.Chinese Acad Sci UCAS, Beijing 100049, Peoples R China 2.Chinese Acad Sci, State Key Lab Drug Res, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China 3.Chinese Acad Sci, Ctr Pharmaceut, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China 4.Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Liaoning, Peoples R China 5.Chinese Acad Med Sci, Ctr Syst Med, Inst Basic Med Sci, Beijing 100005, Peoples R China 6.Peking Union Med Coll, Beijing 100005, Peoples R China 7.Suzhou Inst Syst Med, Suzhou 215123, Jiangsu, Peoples R China |
推荐引用方式 GB/T 7714 | Zhou, Fangyuan,Feng, Bing,Yu, Haijun,et al. Tumor Microenvironment-Activatable Prodrug Vesicles for Nanoenabled Cancer Chemoimmunotherapy Combining Immunogenic Cell Death Induction and CD47 Blockade[J]. ADVANCED MATERIALS,2019,31(14):11. |
APA | Zhou, Fangyuan.,Feng, Bing.,Yu, Haijun.,Wang, Dangge.,Wang, Tingting.,...&Li, Yaping.(2019).Tumor Microenvironment-Activatable Prodrug Vesicles for Nanoenabled Cancer Chemoimmunotherapy Combining Immunogenic Cell Death Induction and CD47 Blockade.ADVANCED MATERIALS,31(14),11. |
MLA | Zhou, Fangyuan,et al."Tumor Microenvironment-Activatable Prodrug Vesicles for Nanoenabled Cancer Chemoimmunotherapy Combining Immunogenic Cell Death Induction and CD47 Blockade".ADVANCED MATERIALS 31.14(2019):11. |
入库方式: OAI收割
来源:上海药物研究所
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