RBD-Modified Bacterial Vesicles Elicited Potential Protective Immunity against SARS-CoV-2

被引:25
作者
Yang, Zhongqian [1 ]
Hua, Liangqun [1 ,2 ]
Yang, Mengli [3 ]
Liu, Shu-Qun [2 ,4 ,5 ]
Shen, Jianxin [2 ,4 ,5 ]
Li, Weiran [1 ]
Long, Qiong [1 ]
Bai, Hongmei [1 ]
Yang, Xu [1 ]
Ren, Zhaoling [6 ,7 ]
Zheng, Xiao [1 ,2 ]
Sun, Wenjia [1 ]
Ye, Chao [1 ]
Li, Duo [1 ,8 ]
Zheng, Peng [1 ]
He, Jinrong [1 ,7 ]
Chen, Yongjun [1 ]
Huang, Weiwei [1 ]
Peng, Xiaozhong [3 ,9 ]
Ma, Yanbing [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Biol, Lab Mol Immunol, Kunming, Yunnan, Peoples R China
[2] Yunnan Univ, Kunming, Yunnan, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Biol, Natl Kunming High Level Biosafety Primate Res Ctr, Kunming, Yunnan, Peoples R China
[4] Yunnan Univ, State Key Lab Conservat & Utilizat Bioresources Y, Kunming, Yunnan, Peoples R China
[5] Yunnan Univ, Sch Life Sci, Kunming, Yunnan, Peoples R China
[6] Kunming Med Univ, Affiliated Hosp 2, Kunming, Yunnan, Peoples R China
[7] Kunming Med Univ, Kunming, Yunnan, Peoples R China
[8] Yunnan Prov Ctr Dis Control & Prevent, Dept Acute Infect Dis Control & Prevent, Kunming, Yunnan, Peoples R China
[9] Chinese Acad Med Sci, Peking Union Med Coll, State Key Lab Med Mol Biol,Neurosci Ctr,Sch Basic, Dept Mol Biol & Biochem,Inst Basic Med Sci,Med Pr, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Bacterial vesicles; receptor binding domain; SARS-CoV-2; vaccine; COVID-19; OUTER-MEMBRANE VESICLES; CELLULAR-IMMUNITY; VACCINES; MATURATION;
D O I
10.1021/acs.nanolett.1c00680
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The disease caused by SARS-CoV-2 infection threatens human health. In this study, we used high-pressure homogenization technology not only to efficiently drive the bacterial membrane to produce artificial vesicles but also to force the fusion protein ClyA-receptor binding domain (RBD) to pass through gaps in the bacterial membrane to increase the contact between ClyA-RBD and the membrane. Therefore, the load of ClyA-RBD on the membrane is substantially increased. Using this technology, we constructed a "ring-like" bacterial biomimetic vesicle (BBV) loaded with polymerized RBD (RBD-BBV). RBD-BBVs injected subcutaneously can accumulate in lymph nodes, promote antigen uptake and processing, and elicit SARS-CoV-2-specific humoral and cellular immune responses in mice. In conclusion, we evaluated the potential of this novel bacterial vesicle as a vaccine delivery system and provided a new idea for the development of SARS-CoV-2 vaccines.
引用
收藏
页码:5920 / 5930
页数:11
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