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单剂量鼻内给予AdCOVID可引发针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的全身和黏膜免疫,并完全保护小鼠免受致死性攻击。

Single-Dose Intranasal Administration of AdCOVID Elicits Systemic and Mucosal Immunity against SARS-CoV-2 and Fully Protects Mice from Lethal Challenge.

作者信息

King R Glenn, Silva-Sanchez Aaron, Peel Jessica N, Botta Davide, Dickson Alexandria M, Pinto Amelia K, Meza-Perez Selene, Allie S Rameeza, Schultz Michael D, Liu Mingyong, Bradley John E, Qiu Shihong, Yang Guang, Zhou Fen, Zumaquero Esther, Simpler Thomas S, Mousseau Betty, Killian John T, Dean Brittany, Shang Qiao, Tipper Jennifer L, Risley Christopher A, Harrod Kevin S, Feng Tsungwei, Lee Young, Shiberu Bethlehem, Krishnan Vyjayanthi, Peguillet Isabelle, Zhang Jianfeng, Green Todd J, Randall Troy D, Suschak John J, Georges Bertrand, Brien James D, Lund Frances E, Roberts M Scot

机构信息

Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Department of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

Vaccines (Basel). 2021 Aug 9;9(8):881. doi: 10.3390/vaccines9080881.

Abstract

The coronavirus disease 2019 (COVID-19) pandemic has highlighted the urgent need for effective prophylactic vaccination to prevent the spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Intranasal vaccination is an attractive strategy to prevent COVID-19 as the nasal mucosa represents the first-line barrier to SARS-CoV-2 entry. The current intramuscular vaccines elicit systemic immunity but not necessarily high-level mucosal immunity. Here, we tested a single intranasal dose of our candidate adenovirus type 5-vectored vaccine encoding the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein (AdCOVID) in inbred, outbred, and transgenic mice. A single intranasal vaccination with AdCOVID elicited a strong and focused immune response against RBD through the induction of mucosal IgA in the respiratory tract, serum neutralizing antibodies, and CD4 and CD8 T cells with a T1-like cytokine expression profile. A single AdCOVID dose resulted in immunity that was sustained for over six months. Moreover, a single intranasal dose completely protected K18-hACE2 mice from lethal SARS-CoV-2 challenge, preventing weight loss and mortality. These data show that AdCOVID promotes concomitant systemic and mucosal immunity and represents a promising vaccine candidate.

摘要

2019年冠状病毒病(COVID-19)大流行凸显了迫切需要有效的预防性疫苗接种以防止严重急性呼吸综合征冠状病毒2(SARS-CoV-2)传播。鼻内接种是预防COVID-19的一种有吸引力的策略,因为鼻黏膜是SARS-CoV-2进入的第一道防线。目前的肌肉注射疫苗可引发全身免疫,但不一定能产生高水平的黏膜免疫。在此,我们在近交系、远交系和转基因小鼠中测试了单剂量鼻内接种我们的候选5型腺病毒载体疫苗,该疫苗编码SARS-CoV-2刺突蛋白受体结合域(RBD)(AdCOVID)。单次鼻内接种AdCOVID通过诱导呼吸道黏膜IgA、血清中和抗体以及具有T1样细胞因子表达谱的CD4和CD8 T细胞,引发了针对RBD的强烈且集中的免疫反应。单剂量AdCOVID产生的免疫力可持续超过六个月。此外,单次鼻内剂量完全保护K18-hACE2小鼠免受致死性SARS-CoV-2攻击,防止体重减轻和死亡。这些数据表明AdCOVID可促进全身和黏膜免疫协同发生,是一种有前景的候选疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c697/8402488/e8c32ece88e8/vaccines-09-00881-g001.jpg

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