McMillan Christopher L D, Azuar Armira, Choo Jovin J Y, Modhiran Naphak, Amarilla Alberto A, Isaacs Ariel, Honeyman Kate E, Cheung Stacey T M, Liang Benjamin, Wurm Maria J, Pino Paco, Kint Joeri, Fernando Germain J P, Landsberg Michael J, Khromykh Alexander A, Hobson-Peters Jody, Watterson Daniel, Young Paul R, Muller David A
School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia.
ExcellGene SA, CH1870 Monthey, Switzerland.
Vaccines (Basel). 2022 Apr 8;10(4):578. doi: 10.3390/vaccines10040578.
The ongoing coronavirus disease 2019 (COVID-19) pandemic continues to disrupt essential health services in 90 percent of countries today. The spike (S) protein found on the surface of the causative agent, the SARS-CoV-2 virus, has been the prime target for current vaccine research since antibodies directed against the S protein were found to neutralize the virus. However, as new variants emerge, mutations within the spike protein have given rise to potential immune evasion of the response generated by the current generation of SARS-CoV-2 vaccines. In this study, a modified, HexaPro S protein subunit vaccine, delivered using a needle-free high-density microarray patch (HD-MAP), was investigated for its immunogenicity and virus-neutralizing abilities. Mice given two doses of the vaccine candidate generated potent antibody responses capable of neutralizing the parental SARS-CoV-2 virus as well as the variants of concern, Alpha and Delta. These results demonstrate that this alternative vaccination strategy has the potential to mitigate the effect of emerging viral variants.
目前,2019年冠状病毒病(COVID-19)大流行仍在扰乱全球90%国家的基本医疗服务。导致该疾病的病原体——严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒表面的刺突(S)蛋白,一直是当前疫苗研究的主要靶点,因为针对S蛋白的抗体被发现可中和该病毒。然而,随着新变种的出现,刺突蛋白内的突变导致了当前一代SARS-CoV-2疫苗所产生的免疫反应可能出现免疫逃逸。在本研究中,使用无针高密度微阵列贴片(HD-MAP)递送的一种经过修饰的六聚体Pro S蛋白亚单位疫苗,对其免疫原性和病毒中和能力进行了研究。接种两剂候选疫苗的小鼠产生了强效抗体反应,能够中和原始SARS-CoV-2病毒以及值得关注的变种——阿尔法和德尔塔。这些结果表明,这种替代疫苗接种策略有可能减轻新出现的病毒变种的影响。