Mucker Eric M, Brocato Rebecca L, Principe Lucia M, Kim Robert K, Zeng Xiankun, Smith Jeffrey M, Kwilas Steven A, Kim Sungwon, Horton Helen, Caproni Lisa, Hooper Jay W
Virology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.
Pathology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.
Vaccines (Basel). 2022 Jul 9;10(7):1104. doi: 10.3390/vaccines10071104.
To combat the COVID-19 pandemic, an assortment of vaccines has been developed. Nucleic acid vaccines have the advantage of rapid production, as they only require a viral antigen sequence and can readily be modified to detected viral mutations. Doggybone™ DNA vaccines targeting the spike protein of SARS-CoV-2 have been generated and compared with a traditionally manufactured, bacterially derived plasmid DNA vaccine that utilizes the same spike sequence. Administered to Syrian hamsters by jet injection at two dose levels, the immunogenicity of both DNA vaccines was compared following two vaccinations. Immunized hamsters were then immunosuppressed and exposed to SARS-CoV-2. Significant differences in body weight were observed during acute infection, and lungs collected at the time of euthanasia had significantly reduced viral RNA, infectious virus, and pathology compared with irrelevant DNA-vaccinated controls. Moreover, immune serum from vaccinated animals was capable of neutralizing SARS-CoV-2 variants of interest and importance in vitro. These data demonstrate the efficacy of a synthetic DNA vaccine approach to protect hamsters from SARS-CoV-2.
为抗击新冠疫情,已研发出多种疫苗。核酸疫苗具有生产速度快的优势,因为它们只需要病毒抗原序列,并且可以很容易地进行修改以检测病毒突变。已制备出针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白的Doggybone™DNA疫苗,并与一种利用相同刺突序列的传统制造的细菌衍生质粒DNA疫苗进行了比较。以两种剂量水平通过喷射注射法给叙利亚仓鼠接种疫苗,在两次接种后比较了两种DNA疫苗的免疫原性。然后对免疫后的仓鼠进行免疫抑制,并使其接触SARS-CoV-2。在急性感染期间观察到体重有显著差异,与接种无关DNA疫苗的对照组相比,安乐死时采集的肺部组织中的病毒RNA、传染性病毒和病理学表现均显著降低。此外,接种疫苗动物的免疫血清在体外能够中和具有重要意义的SARS-CoV-2变异株。这些数据证明了合成DNA疫苗方法在保护仓鼠免受SARS-CoV-2感染方面的有效性。