Glycosylated Delta-receptor-binding domain mucosal vaccine elicits broadly neutralizing antibodies with protection against SARS-CoV-2 challenge

被引:6
|
作者
Guan, Xiaoqing [1 ]
Verma, Abhishek K. [2 ]
Wang, Gang [1 ]
Shi, Juan [1 ]
Perlman, Stanley [2 ,3 ]
Du, Lanying [1 ]
机构
[1] Georgia State Univ, Inst Biomed Sci, Atlanta, GA 30302 USA
[2] Univ Iowa, Dept Microbiol & Immunol, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
关键词
SPIKE PROTEIN; COVID-19; COV;
D O I
10.1016/j.isci.2023.108033
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
Mucosal COVID-19 vaccines are needed to block SARS-CoV-2 infection at the mucosal site. Intranasal delivery of a glycosylated Delta variant receptor-binding domain (Delta-RBD) mucosal vaccine elicited potent and balanced systemic antibody titers comparable to those induced by the intramuscular injection of the same vaccine or Omicron-S subunit vaccine, as well as high mucosal IgA antibody responses. It elicited broadly neutralizing antibodies against the original SARS-CoV-2 strain, Delta and Omicron BA1/BA2 variants, completely protecting transgenic mice from lethal challenge with a Delta variant, including complete absence of weight loss. Of note, intramuscular priming with the Omicron-S protein followed by intranasal boosting with the Delta-RBD protein improved the vaccine's ability to generate broad-spectrum neutralizing antibodies against recent BA5 and XBB Omicron variants. Overall, this vaccine has the poten-tial to prevent the SARS-CoV-2 infection of the respiratory mucosa, while the i.m. priming and i.n. boost-ing vaccination strategy may offer protection against known and emerging SARS-CoV-2 variants.
引用
收藏
页数:12
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