Malherbe Delphine C, Kurup Drishya, Wirblich Christoph, Ronk Adam J, Mire Chad, Kuzmina Natalia, Shaik Noor, Periasamy Sivakumar, Hyde Matthew A, Williams Julie M, Shi Pei-Yong, Schnell Matthias J, Bukreyev Alexander
Department of Pathology, University of Texas Medical Branch, Galveston, TX, USA.
Galveston National Laboratory, Galveston, TX, USA.
NPJ Vaccines. 2021 Jul 22;6(1):91. doi: 10.1038/s41541-021-00352-1.
The development of effective countermeasures against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the agent responsible for the COVID-19 pandemic, is a priority. We designed and produced ConVac, a replication-competent vesicular stomatitis virus (VSV) vaccine vector that expresses the S1 subunit of SARS-CoV-2 spike protein. We used golden Syrian hamsters as animal models of severe COVID-19 to test the efficacy of the ConVac vaccine. A single vaccine dose elicited high levels of SARS-CoV-2 specific binding and neutralizing antibodies; following intranasal challenge with SARS-CoV-2, animals were protected from weight loss and viral replication in the lungs. No enhanced pathology was observed in vaccinated animals upon challenge, but some inflammation was still detected. The data indicate rapid control of SARS-CoV-2 replication by the S1-based VSV-vectored SARS-CoV-2 ConVac vaccine.
研发针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2,即导致COVID-19大流行的病原体)的有效对策是当务之急。我们设计并生产了ConVac,这是一种具有复制能力的水泡性口炎病毒(VSV)疫苗载体,可表达SARS-CoV-2刺突蛋白的S1亚基。我们使用金黄叙利亚仓鼠作为重症COVID-19的动物模型来测试ConVac疫苗的疗效。单剂量疫苗引发了高水平的SARS-CoV-2特异性结合和中和抗体;在用SARS-CoV-2进行鼻内攻击后,动物受到保护,体重未减轻,肺部也未发生病毒复制。在攻击后,接种疫苗的动物未观察到增强的病理变化,但仍检测到一些炎症。数据表明,基于S1的VSV载体SARS-CoV-2 ConVac疫苗可快速控制SARS-CoV-2的复制。