Long-acting vaccine delivery systems

被引:13
|
作者
Walvekar, Pavan [1 ]
Kumar, Pradeep [1 ]
Choonara, Yahya E. [1 ]
机构
[1] Univ Witwatersrand, Fac Hlth Sci, Sch Therapeut Sci, Dept Pharm & Pharmacol,Wits Adv Drug Delivery Plat, 7 York Rd, ZA-2193 Parktown, South Africa
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
Long-acting vaccines; Biomaterials; Sustained delivery; Immunogenicity; Immunotherapy; N-TRIMETHYL CHITOSAN; CD8; T-CELLS; GERMINAL CENTER; IN-VIVO; DENDRITIC CELLS; PLASMID DNA; ANTIGEN; DRUG; NANOPARTICLES; RESPONSES;
D O I
10.1016/j.addr.2023.114897
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bolus vaccines are often administered multiple times due to rapid clearance and reduced transportation to draining lymph nodes resulting in inadequate activation of T and B lymphocytes. In order to achieve adaptive immunity, prolonged exposure of antigens to these immune cells is crucial. Recent research has been focusing on developing long-acting biomaterial-based vaccine delivery systems, which can modulate the release of encapsulated antigens or epitopes to facilitate enhanced antigen presentation in lymph nodes and subsequently achieve robust T and B cell responses. Over the past few years, various polymers and lipids have been extensively explored to develop effective biomaterial-based vaccine strategies. The article reviews relevant polymer and lipid-based strategies used to prepare long-acting vaccine carriers and discusses their results concerning immune responses.(c) 2023 Elsevier B.V. All rights reserved.
引用
收藏
页数:25
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