Hitchhiking on Controlled-Release Drug Delivery Systems: Opportunities and Challenges for Cancer Vaccines

被引:17
|
作者
Han, Lu [1 ]
Peng, Ke [2 ]
Qiu, Li-Ying [1 ]
Li, Meng [1 ]
Ruan, Jing-Hua [3 ]
He, Li-Li [1 ]
Yuan, Zhi-Xiang [1 ]
机构
[1] Southwest Minzu Univ, Coll Pharm, Chengdu, Peoples R China
[2] Queens Univ Belfast, Sch Pharm, Belfast, Antrim, North Ireland
[3] Guizhou Univ Tradit Chinese Med, Affiliated Hosp 1, Guiyang, Peoples R China
基金
中国国家自然科学基金;
关键词
cancer vaccine; in situ vaccination; drug delivery system; controlled release; sustained release; hydrogel; microneedle; SYNTHETIC LONG PEPTIDES; IMMUNOGENIC CELL-DEATH; DENDRITIC CELLS; IMMUNE-RESPONSES; CO-DELIVERY; IN-VIVO; INJECTABLE HYDROGELS; SURFACE MODIFICATION; PLGA-MICROSPHERES; ANTIGEN RELEASE;
D O I
10.3389/fphar.2021.679602
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cancer vaccines represent among the most promising strategies in the battle against cancers. However, the clinical efficacy of current cancer vaccines is largely limited by the lack of optimized delivery systems to generate strong and persistent antitumor immune responses. Moreover, most cancer vaccines require multiple injections to boost the immune responses, leading to poor patient compliance. Controlled-release drug delivery systems are able to address these issues by presenting drugs in a controlled spatiotemporal manner, which allows co-delivery of multiple drugs, reduction of dosing frequency and avoidance of significant systemic toxicities. In this review, we outline the recent progress in cancer vaccines including subunit vaccines, genetic vaccines, dendritic cell-based vaccines, tumor cell-based vaccines and in situ vaccines. Furthermore, we highlight the efforts and challenges of controlled or sustained release drug delivery systems (e.g., microparticles, scaffolds, injectable gels, and microneedles) in ameliorating the safety, effectiveness and operability of cancer vaccines. Finally, we briefly discuss the correlations of vaccine release kinetics and the immune responses to enlighten the rational design of the next-generation platforms for cancer therapy.
引用
收藏
页数:19
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