Saponin nanoparticle adjuvants incorporating Toll-like receptor agonists drive distinct immune signatures and potent vaccine responses

被引:1
|
作者
Ou, Ben S. [1 ]
Baillet, Julie [2 ]
Interrante, Maria V. Filsinger [3 ,4 ,5 ]
Adamska, Julia Z. [6 ]
Zhou, Xueting [1 ]
Saouaf, Olivia M. [2 ]
Yan, Jerry [1 ]
Klich, John H. [1 ]
Jons, Carolyn K. [2 ]
Meany, Emily L. [1 ]
Valdez, Adian S. [7 ,8 ]
Carter, Lauren [7 ,8 ]
Pulendran, Bali [6 ,9 ,10 ]
King, Neil P. [7 ,8 ]
Appel, Eric A. [1 ,2 ,3 ,6 ,11 ,12 ]
机构
[1] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[3] Stanford Univ, Stanford ChEM H, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Stanford Biophys Program, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Stanford Med Scientist Training Program, Stanford, CA 94305 USA
[6] Stanford Univ, Sch Med, Inst Immun Transplantat & Infect, Stanford, CA 94305 USA
[7] Univ Washington, Dept Biochem, Seattle, WA 98109 USA
[8] Univ Washington, Inst Prot Design, Seattle, WA 98195 USA
[9] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[10] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[11] Stanford Univ, Sch Med, Dept Pediat Endocrinol, Stanford, CA 94305 USA
[12] Stanford Univ, Woods Inst Environm, Stanford, CA 94305 USA
来源
SCIENCE ADVANCES | 2024年 / 10卷 / 32期
基金
美国国家卫生研究院; 美国国家科学基金会; 比尔及梅琳达.盖茨基金会;
关键词
NEUTRALIZING ANTIBODY-RESPONSES; TLR AGONISTS; VISUALIZATION; MATRICES; SYSTEM;
D O I
10.1126/sciadv.adn7187
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Over the past few decades, the development of potent and safe immune-activating adjuvant technologies has become the heart of intensive research in the constant fight against highly mutative and immune evasive viruses such as influenza, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and human immunodeficiency virus (HIV). Herein, we developed a highly modular saponin-based nanoparticle platform incorporating Toll-like receptor agonists (TLRas) including TLR1/2a, TLR4a, and TLR7/8a adjuvants and their mixtures. These various TLRa-saponin nanoparticle adjuvant constructs induce unique acute cytokine and immune-signaling profiles, leading to specific T helper responses that could be of interest depending on the target disease for prevention. In a murine vaccine study, the adjuvants greatly improved the potency, durability, breadth, and neutralization of both COVID-19 and HIV vaccine candidates, suggesting the potential broad application of these adjuvant constructs to a range of different antigens. Overall, this work demonstrates a modular TLRa-SNP adjuvant platform that could improve the design of vaccines and affect modern vaccine development.
引用
收藏
页数:18
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