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表达二聚体串联重复刺突蛋白 RBD 的重组黑猩猩腺病毒 AdC7 可保护小鼠免受 COVID-19 侵害。

Recombinant chimpanzee adenovirus AdC7 expressing dimeric tandem-repeat spike protein RBD protects mice against COVID-19.

机构信息

Key Laboratory of Tropical Translational Medicine of Ministry of Education, School of Tropical Medicine and Laboratory Medicine, The First Affiliated Hospital, Hainan Medical University, Haikou, People's Republic of China.

Research Network of Immunity and Health (RNIH), Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing, People's Republic of China.

出版信息

Emerg Microbes Infect. 2021 Dec;10(1):1574-1588. doi: 10.1080/22221751.2021.1959270.

Abstract

A safe and effective vaccine is urgently needed to control the unprecedented COVID-19 pandemic. Four adenovirus-vectored vaccines expressing spike (S) protein have been approved for use. Here, we generated several recombinant chimpanzee adenovirus (AdC7) vaccines expressing S, receptor-binding domain (RBD), or tandem-repeat dimeric RBD (RBD-tr2). We found vaccination via either intramuscular or intranasal route was highly immunogenic in mice to elicit both humoral and cellular immune responses. AdC7-RBD-tr2 showed higher antibody responses compared to either AdC7-S or AdC7-RBD. Intranasal administration of AdC7-RBD-tr2 additionally induced mucosal immunity with neutralizing activity in bronchoalveolar lavage fluid. Either single-dose or two-dose mucosal administration of AdC7-RBD-tr2 protected mice against SARS-CoV-2 challenge, with undetectable subgenomic RNA in lung and relieved lung injury. AdC7-RBD-tr2-elicted sera preserved the neutralizing activity against the circulating variants, especially the Delta variant. These results support AdC7-RBD-tr2 as a promising COVID-19 vaccine candidate.

摘要

急需安全有效的疫苗来控制前所未有的 COVID-19 大流行。已经批准了四种表达刺突(S)蛋白的腺病毒载体疫苗。在这里,我们生成了几种表达 S、受体结合域(RBD)或串联重复二聚体 RBD(RBD-tr2)的重组黑猩猩腺病毒(AdC7)疫苗。我们发现,通过肌肉内或鼻内途径接种疫苗在小鼠中具有高度免疫原性,可引发体液和细胞免疫反应。与 AdC7-S 或 AdC7-RBD 相比,AdC7-RBD-tr2 显示出更高的抗体反应。AdC7-RBD-tr2 的鼻内给药还诱导了支气管肺泡灌洗液中的粘膜免疫和中和活性。单次或两次鼻内给予 AdC7-RBD-tr2 可保护小鼠免受 SARS-CoV-2 攻击,肺部亚基因组 RNA 检测不到,并缓解肺部损伤。AdC7-RBD-tr2 诱导的血清保留了对循环变异体的中和活性,尤其是 Delta 变异体。这些结果支持 AdC7-RBD-tr2 作为一种有前途的 COVID-19 疫苗候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de6/8366625/c8b04dc8eac6/TEMI_A_1959270_F0001_OC.jpg

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