Overcoming challenges in the delivery of STING agonists for cancer immunotherapy: A comprehensive review of strategies and future perspectives

被引:15
|
作者
Huang, Cuiqing [1 ,2 ]
Shao, Ni [1 ]
Huang, Yanyu [3 ]
Chen, Jifeng [1 ]
Wang, Duo [1 ]
Hu, Genwen [1 ,4 ]
Zhang, Hong [5 ]
Luo, Liangping [1 ]
Xiao, Zeyu [1 ]
机构
[1] Jinan Univ, Affiliated Hosp 1, Guangzhou Key Lab Mol & Funct Imaging Clin Transla, Guangzhou 510632, Peoples R China
[2] Guangdong Women & Children Hosp, Dept Ultrasound, Guangzhou 511400, Peoples R China
[3] Univ Calif Davis, Dept Biochem & Mol Med, Sacramento, CA 95817 USA
[4] Jinan Univ, Shenzhen Peoples Hosp, Clin Med Coll 2, Dept Radiol, Shenzhen 518020, Peoples R China
[5] Jinan Univ, Affiliated Hosp 6, Dept Intervent Vasc Surg, Dongguan 523560, Peoples R China
关键词
STING agonists; Nanoprecipitation; Self; -assembly; Hydrogel; Cancer immunotherapy; TUMOR MICROENVIRONMENT; BIODEGRADABLE HYDROGELS; CYCLIC DINUCLEOTIDE; CONTROLLED-RELEASE; IMMUNE AGONISTS; INNATE IMMUNITY; NANOPARTICLES; COMBINATION; THERAPY; CELLS;
D O I
10.1016/j.mtbio.2023.100839
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
STING (Stimulator of Interferon Genes) agonists have emerged as promising agents in the field of cancer immunotherapy, owing to their excellent capacity to activate the innate immune response and combat tumorinduced immunosuppression. This review provides a comprehensive exploration of the strategies employed to develop effective formulations for STING agonists, with particular emphasis on versatile nano-delivery systems. The recent advancements in delivery systems based on lipids, natural/synthetic polymers, and proteins for STING agonists are summarized. The preparation methodologies of nanoprecipitation, self-assembly, and hydrogel, along with their advantages and disadvantages, are also discussed. Furthermore, the challenges and opportunities in developing next-generation STING agonist delivery systems are elaborated. This review aims to serve as a reference for researchers in designing novel and effective STING agonist delivery systems for cancer immunotherapy.
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页数:18
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