DNA Nanomaterials-Based Platforms for Cancer Immunotherapy

被引:19
|
作者
Tian, Run [1 ,2 ,3 ]
Shang, Yingxu [1 ]
Wang, Yiming [1 ]
Jiang, Qiao [1 ,2 ]
Ding, Baoquan [1 ,2 ,4 ]
机构
[1] Natl Ctr Nano Sci & Technol, CAS Key Lab Nanosyst & Hierarch Fabricat, CAS Ctr Excellence Nanosci, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Sci, Beijing 100049, Peoples R China
[3] Univ Chinese Acad Sci, Sino Danish Ctr Educ & Res, Sino Danish Coll, Beijing 100049, Peoples R China
[4] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450001, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
cancer immunotherapy; DNA nanomaterials; immune cell engineering; immunogenic cell death; nanovaccines; IMMUNOGENIC CELL-DEATH; ORIGAMI NANOSTRUCTURES; INTRACELLULAR DELIVERY; EFFICIENT DELIVERY; IN-VITRO; CPG; ACID; NANOTECHNOLOGY; VEHICLES; DESIGN;
D O I
10.1002/smtd.202201518
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The past few decades have witnessed the evolving paradigm for cancer therapy from nonspecific cytotoxic agents to selective, mechanism-based therapeutics, especially immunotherapy. In particular, the integration of nanomaterials with immunotherapy is proven to improve the therapeutic outcome and minimize off-target toxicity in the treatment. As a novel nanomaterial, DNA-based self-assemblies featuring uniform geometries, feasible modifications, programmability, surface addressability, versatility, and intrinsic biocompatibility, are extensively exploited for innovative and effective cancer immunotherapy. In this review, the successful employment of DNA nanoplatforms for cancer immunotherapy, including the delivery of immunogenic cell death inducers, adjuvants and vaccines, immune checkpoint blockers as well as the application in immune cell engineering and adoptive cell therapy is summarized. The remaining challenges and future perspectives regarding the pharmacokinetics/pharmacodynamics, in vivo fate and immunogenicity of DNA materials, and the design of intelligent DNA nanomedicine for individualized cancer immunotherapy are also discussed.
引用
收藏
页数:20
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