Enhancing anti-PD-1 Immunotherapy by Nanomicelles Self-Assembled from Multivalent Aptamer Drug Conjugates

被引:54
|
作者
Geng, Zhongmin [1 ]
Wang, Lu [1 ]
Liu, Ke [1 ]
Liu, Jinyao [1 ,2 ]
Tan, Weihong [1 ]
机构
[1] Shanghai Jiao Tong Univ, Renji Hosp, State Key Lab Oncogenes & Related Genes,Inst Mol, Shanghai Key Lab Nucle Acid Chem & Nanomed,Sch Me, Shanghai 200127, Peoples R China
[2] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Shanghai Key Lab Gynecol Oncol, Shanghai 200127, Peoples R China
基金
中国国家自然科学基金;
关键词
multivalent aptamer drugs; co-self-assembly; immunotherapy; nanomicelles; tumor-targeting ability; IMMUNOGENIC CELL-DEATH; CHECKPOINT BLOCKADE; TUMOR MICROENVIRONMENT; PHOTOTHERMAL THERAPY; IMMUNE-ADJUVANT; CANCER; NANOPARTICLES; DELIVERY; CHEMOTHERAPY; DOXORUBICIN;
D O I
10.1002/anie.202102631
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A tumor-targeting enhanced chemotherapy, enabled by aptamer-drug conjugate nanomicelles, is reported that boosts antitumor immune responses. Multivalent aptamer drug conjugate (ApMDC), an amphiphilic telodendrimer consisting of a hydrophilic aptamer and a hydrophobic monodendron anchored with four anticancer drugs by acid-labile linkers, was designed and synthesized. By co-self-assembly with an ApMDC analogue, in which aptamer is replaced with polyethylene glycol, the surface aptamer density of these nanomicelles can be screened to reach an optimal complementation between blood circulation and tumor-targeting ability. Optimized nanomicelles can enhance immunogenic cell death of tumor cells, which strikingly augments the tumor-specific immune responses of the checkpoint blockade in immunocompetent tumor-bearing mice. ApMDC nanomicelles represent a robust platform for structure-function optimization of drug conjugates and nanomedicines.
引用
收藏
页码:15459 / 15465
页数:7
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