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Neutralizing antibody against severe acute respiratory syndrome (SARS)-coronavirus spike is highly effective for the protection of mice in the murine SARS model

机译:抗严重急性呼吸综合征(SARS)-冠状病毒高峰的中和抗体对鼠SARS模型中的小鼠具有高度保护作用

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We evaluated the efficacy of three SARS vaccine candidates in a murine SARS model utilizing low-virulence Pp and SARS-CoV coinfection. Vaccinated mice were protected from severe respiratory disease in parallel with a low virus titer in the lungs and a high neutralizing antibody titer in the plasma. Importantly, the administration of spike protein-specific neutralizing monoclonal antibody protected mice from the disease, indicating that the neutralization is sufficient for protection. Moreover, a high level of IL-6 and MCP-1 production, but not other 18 cytokines tested, on days 2 and 3 after SARS-CoV infection was closely linked to the virus replication and disease severity, suggesting the importance of these cytokines in the lung pathogenicity of SARS-CoV infection.
机译:我们在利用低毒力Pp和SARS-CoV共感染的鼠SARS模型中评估了三种SARS候选疫苗的功效。接种疫苗的小鼠受到保护,免受严重的呼吸道疾病的侵害,同时肺部病毒滴度低,血浆中和抗体滴度高。重要的是,施用刺突蛋白特异性中和单克隆抗体可保护小鼠免受疾病侵袭,表明中和足以保护小鼠。此外,SARS-CoV感染后第2天和第3天,高水平的IL-6和MCP-1产生,但未测试其他18种细胞因子,与病毒复制和疾病严重程度密切相关,这表明这些细胞因子的重要性SARS-CoV感染的肺致病性。

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