Sun Weina, McCroskery Stephen, Liu Wen-Chun, Leist Sarah R, Liu Yonghong, Albrecht Randy A, Slamanig Stefan, Oliva Justine, Amanat Fatima, Schäfer Alexandra, Dinnon Kenneth H, Innis Bruce L, García-Sastre Adolfo, Krammer Florian, Baric Ralph S, Palese Peter
Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Global Health Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Vaccines (Basel). 2020 Dec 17;8(4):771. doi: 10.3390/vaccines8040771.
A successful severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine must not only be safe and protective, but must also meet the demand on a global scale at a low cost. Using the current influenza virus vaccine production capacity to manufacture an egg-based inactivated Newcastle disease virus (NDV)/SARS-CoV-2 vaccine would meet that challenge. Here, we report pre-clinical evaluations of an inactivated NDV chimera stably expressing the membrane-anchored form of the spike (NDV-S) as a potent coronavirus disease 2019 (COVID-19) vaccine in mice and hamsters. The inactivated NDV-S vaccine was immunogenic, inducing strong binding and/or neutralizing antibodies in both animal models. More importantly, the inactivated NDV-S vaccine protected animals from SARS-CoV-2 infections. In the presence of an adjuvant, antigen-sparing could be achieved, which would further reduce the cost while maintaining the protective efficacy of the vaccine.
一种成功的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗不仅必须安全且具有保护作用,还必须以低成本满足全球范围内的需求。利用当前流感病毒疫苗的生产能力来制造基于鸡蛋的灭活新城疫病毒(NDV)/SARS-CoV-2疫苗将应对这一挑战。在此,我们报告了一种稳定表达刺突蛋白膜锚定形式的灭活NDV嵌合体(NDV-S)作为一种有效的2019冠状病毒病(COVID-19)疫苗在小鼠和仓鼠中的临床前评估。灭活的NDV-S疫苗具有免疫原性,在两种动物模型中均诱导产生了强结合和/或中和抗体。更重要的是,灭活的NDV-S疫苗保护动物免受SARS-CoV-2感染。在佐剂存在的情况下,可以实现抗原节约,这将在保持疫苗保护效力的同时进一步降低成本。