Seo Yong Bok, Suh You Suk, Ryu Ji In, Jang Hwanhee, Oh Hanseul, Koo Bon-Sang, Seo Sang-Hwan, Hong Jung Joo, Song Manki, Kim Sung-Joo, Sung Young Chul
Research Institute, SL VaxiGen Inc., Korea Bio Park, Seongnam 13488, Korea.
Research Institute, Genexine Inc., Korea Bio Park, Seongnam 13488, Korea.
Vaccines (Basel). 2021 Mar 24;9(4):307. doi: 10.3390/vaccines9040307.
The unprecedented and rapid spread of SARS-CoV-2 (severe acute respiratory syndrome-coronavirus-2) has motivated the need for a rapidly producible and scalable vaccine. Here, we developed a synthetic soluble SARS-CoV-2 spike (S) DNA-based vaccine candidate, GX-19. In mice, immunization with GX-19 elicited not only S-specific systemic and pulmonary antibody responses but also Th1-biased T cell responses in a dose-dependent manner. GX-19-vaccinated nonhuman primates seroconverted rapidly and exhibited a detectable neutralizing antibody response as well as multifunctional CD4+ and CD8+ T cell responses. Notably, when the immunized nonhuman primates were challenged at 10 weeks after the last vaccination with GX-19, they had reduced viral loads in contrast to non-vaccinated primates as a control. These findings indicate that GX-19 vaccination provides a durable protective immune response and also support further development of GX-19 as a vaccine candidate for SARS-CoV-2.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)前所未有的快速传播促使人们需要一种能够快速生产且可扩展的疫苗。在此,我们开发了一种基于合成可溶性SARS-CoV-2刺突(S)蛋白DNA的候选疫苗GX-19。在小鼠中,用GX-19免疫不仅引发了S特异性的全身和肺部抗体反应,还以剂量依赖的方式引发了偏向Th1的T细胞反应。接种GX-19的非人灵长类动物迅速产生血清转化,并表现出可检测到的中和抗体反应以及多功能CD4+和CD8+ T细胞反应。值得注意的是,当用GX-19对免疫后的非人灵长类动物在最后一次接种后10周进行攻毒时,与作为对照的未接种灵长类动物相比,它们的病毒载量降低。这些发现表明,接种GX-19可提供持久的保护性免疫反应,也支持将GX-19进一步开发为SARS-CoV-2的候选疫苗。