Next-generation nanovaccine induces durable immunity and protects against SARS-CoV-2

被引:0
|
作者
Ross, Kathleen A. [1 ]
Kelly, Sean [1 ,2 ]
Phadke, Kruttika S. [3 ]
Peroutka-Bigus, Nathan [3 ]
Fasina, Olufemi [4 ]
Siddoway, Alaric [1 ,2 ]
Mallapragada, Surya K. [1 ,2 ]
Wannemuehler, Michael J. [1 ,3 ]
Bellaire, Bryan H. [1 ,3 ]
Narasimhan, Balaji [1 ,2 ]
机构
[1] Iowa State Univ, Nanovaccine Inst, Ames, IA 50011 USA
[2] Iowa State Univ, Chem & Biol Engn, Ames, IA 50011 USA
[3] Iowa State Univ, Vet Microbiol & Prevent Med, Ames, IA 50011 USA
[4] Iowa State Univ, Vet Pathol, Ames, IA 50011 USA
关键词
SARS-CoV-2; Nanovaccine; Neutralizing antibody; Antigen-specific T cell; POLYANHYDRIDE MICROSPHERES; SARS CORONAVIRUS; ANTIBODY; RELEASE; MEMORY;
D O I
10.1016/j.actbio.2024.05.048
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
While first generation SARS-CoV-2 vaccines were effective in slowing the spread and severity of disease during the COVID-19 pandemic, there is a need for vaccines capable of inducing durable and broad immunity against emerging variants of concern. Nanoparticle-based vaccines (i.e., "nanovaccines") composed of polyanhydride nanoparticles and pentablock copolymer micelles have previously been shown to protect against respiratory pathogens, including influenza A virus, respiratory syncytial virus, and Yersinia pestis. In this work, a nanovaccine containing SARS-CoV-2 spike and nucleocapsid antigens was designed and optimized. The optimized nanovaccine induced long-lived systemic IgG antibody responses against wild-type SARS-CoV-2 virus. In addition, the nanovaccine induced antibody responses capable of neutralization and cross-reactivity to multiple SARS-CoV-2 variants (including B.1.1.529) and antigen-specific CD4(+) and CD8(+) T cell responses. Finally, the nanovaccine protected mice against a lethal SARS-CoV-2 challenge, setting the stage for advancing particle-based SARS-CoV-2 nanovaccines.
引用
收藏
页码:318 / 329
页数:12
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