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针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的单次注射腺相关病毒载体疫苗,具有快速和持久的免疫力。

Single-shot AAV-vectored vaccine against SARS-CoV-2 with fast and long-lasting immunity.

作者信息

Wu Fuhua, Luo Shuang, Zhang Yongshun, Ou Yangsen, Wang Hairui, Guo Zhaofei, He Chunting, Bai Shuting, He Penghui, Jiang Min, Chen Xiaoyan, Du Guangsheng, Sun Xun

机构信息

Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

出版信息

Acta Pharm Sin B. 2023 May;13(5):2219-2233. doi: 10.1016/j.apsb.2022.07.004. Epub 2022 Jul 12.

DOI:10.1016/j.apsb.2022.07.004
PMID:35846427
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9273293/
Abstract

Due to the insufficient long-term protection and significant efficacy reduction to new variants of current COVID-19 vaccines, the epidemic prevention and control are still challenging. Here, we employ a capsid and antigen structure engineering (CASE) strategy to manufacture an adeno-associated viral serotype 6-based vaccine (S663V-RBD), which expresses trimeric receptor binding domain (RBD) of spike protein fused with a biological adjuvant RS09. Impressively, the engineered S663V-RBD could rapidly induce a satisfactory RBD-specific IgG titer within 2 weeks and maintain the titer for more than 4 months. Compared to the licensed BBIBP-CorV (Sinopharm, China), a single-dose S663V-RBD induced more endurable and robust immune responses in mice and elicited superior neutralizing antibodies against three typical SARS-CoV-2 pseudoviruses including wild type, C.37 (Lambda) and B.1.617.2 (Delta). More interestingly, the intramuscular injection of S663V-RBD could overcome pre-existing immunity against the capsid. Given its effectiveness, the CASE-based S663V-RBD may provide a new solution for the current and next pandemic.

摘要

由于目前的新冠疫苗长期保护不足且对新变种的效力显著降低,疫情防控仍面临挑战。在此,我们采用衣壳和抗原结构工程(CASE)策略制备了一种基于腺相关病毒6型的疫苗(S663V-RBD),该疫苗表达与生物佐剂RS09融合的刺突蛋白三聚体受体结合域(RBD)。令人印象深刻的是,工程化的S663V-RBD能够在2周内迅速诱导出令人满意的RBD特异性IgG滴度,并将该滴度维持4个月以上。与已获许可的BBIBP-CorV(中国国药集团)相比,单剂量的S663V-RBD在小鼠中诱导了更持久、更强有力的免疫反应,并引发了针对三种典型SARS-CoV-2假病毒(包括野生型、C.37(拉姆达)和B.1.617.2(德尔塔))的卓越中和抗体。更有趣的是,肌肉注射S663V-RBD可以克服对衣壳的预先存在的免疫力。鉴于其有效性,基于CASE的S663V-RBD可能为当前及未来的大流行提供一种新的解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/88f81e004853/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/41ac4a662288/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/cea674db1203/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/e6ee5c4b8fe6/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/38d403b46093/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/89430a111ced/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/64c190b41f55/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/12f3214ca329/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/88f81e004853/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/41ac4a662288/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/cea674db1203/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/e6ee5c4b8fe6/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/38d403b46093/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/89430a111ced/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/64c190b41f55/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/12f3214ca329/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/755f/10213985/88f81e004853/gr7.jpg

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