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两佐剂多抗原候选疫苗诱导针对 SARS-CoV-2 挑战的优越保护免疫应答。

A two-adjuvant multiantigen candidate vaccine induces superior protective immune responses against SARS-CoV-2 challenge.

机构信息

Yunnan Key Laboratory of Vaccine Research and Development on Severe Infectious Diseases, Institute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Kunming, Yunnan, China.

Laboratory of Immunogenetics, Institute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College, Kunming, Yunnan, China.

出版信息

Cell Rep. 2021 Dec 14;37(11):110112. doi: 10.1016/j.celrep.2021.110112. Epub 2021 Nov 24.

DOI:10.1016/j.celrep.2021.110112
PMID:34863353
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8610932/
Abstract

An ideal vaccine against SARS-CoV-2 is expected to elicit broad immunity to prevent viral infection and disease, with efficient viral clearance in the upper respiratory tract (URT). Here, the N protein and prefusion-full S protein (SFL) are combined with flagellin (KF) and cyclic GMP-AMP (cGAMP) to generate a candidate vaccine, and this vaccine elicits stronger systemic and mucosal humoral immunity than vaccines containing other forms of the S protein. Furthermore, the candidate vaccine administered via intranasal route can enhance local immune responses in the respiratory tract. Importantly, human ACE2 transgenic mice given the candidate vaccine are protected against lethal SARS-CoV-2 challenge, with superior protection in the URT compared with that in mice immunized with an inactivated vaccine. In summary, the developed vaccine can elicit a multifaceted immune response and induce robust viral clearance in the URT, which makes it a potential vaccine for preventing disease and infection of SARS-CoV-2.

摘要

一种理想的针对 SARS-CoV-2 的疫苗有望引发广泛的免疫反应,以预防病毒感染和疾病,并在上呼吸道 (URT) 中有效清除病毒。在这里,N 蛋白和融合前全长 S 蛋白 (SFL) 与鞭毛蛋白 (KF) 和环鸟苷酸-腺苷酸 (cGAMP) 结合,生成候选疫苗,该疫苗比包含其他形式 S 蛋白的疫苗引发更强的系统和粘膜体液免疫。此外,通过鼻内途径给予候选疫苗可增强呼吸道的局部免疫反应。重要的是,给予候选疫苗的人 ACE2 转基因小鼠可免受致死性 SARS-CoV-2 攻击,与用灭活疫苗免疫的小鼠相比,在 URT 中具有更好的保护作用。总之,所开发的疫苗可以引发多方面的免疫反应,并在上呼吸道中诱导强大的病毒清除,这使其成为预防 SARS-CoV-2 疾病和感染的潜在疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/acc065316900/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/2f62c4818d65/fx1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/70ac78d239b2/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/aeaf747e0779/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/e45c34ac9fea/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/566c7e2c799d/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/12cd78ee1a9e/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/0355e8a66c77/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/acc065316900/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/2f62c4818d65/fx1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/70ac78d239b2/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/aeaf747e0779/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/e45c34ac9fea/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/566c7e2c799d/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/12cd78ee1a9e/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/0355e8a66c77/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e57/8610932/acc065316900/gr7_lrg.jpg

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