Haun Brien K, Lai Chih-Yun, Williams Caitlin A, Wong Teri Ann, Lieberman Michael M, Pessaint Laurent, Andersen-Elyard Hanne, Lehrer Axel T
bioRxiv. 2020 Jul 26:2020.07.24.220715. doi: 10.1101/2020.07.24.220715.
The current COVID-19 pandemic has claimed hundreds of thousands of lives and its causative agent, SARS-CoV-2, has infected millions, globally. The highly contagious nature of this respiratory virus has spurred massive global efforts to develop vaccines at record speeds. In addition to enhanced immunogen delivery, adjuvants may greatly impact protective efficacy of a SARS-CoV-2 vaccine. To investigate adjuvant suitability, we formulated protein subunit vaccines consisting of the recombinant S1 domain of SARS-CoV-2 Spike protein alone or in combination with either CoVaccine HT™ or Alhydrogel. CoVaccine HT™ induced high titres of antigen-binding IgG after a single dose, facilitated affinity maturation and class switching to a greater extent than Alhydrogel and elicited potent cell-mediated immunity as well as virus neutralising antibody titres. Data presented here suggests that adjuvantation with CoVaccine HT™ can rapidly induce a comprehensive and protective immune response to SARS-CoV-2.
当前的新冠疫情已导致数十万人死亡,其病原体严重急性呼吸综合征冠状病毒2(SARS-CoV-2)在全球范围内感染了数百万人。这种呼吸道病毒的高传染性促使全球以创纪录的速度大力研发疫苗。除了增强免疫原递送外,佐剂可能会极大地影响SARS-CoV-2疫苗的保护效力。为了研究佐剂的适用性,我们制备了蛋白质亚单位疫苗,其由单独的SARS-CoV-2刺突蛋白重组S1结构域组成,或与CoVaccine HT™或氢氧化铝佐剂联合使用。CoVaccine HT™单剂量接种后可诱导产生高滴度的抗原结合IgG,比氢氧化铝佐剂更能促进亲和力成熟和类别转换,并引发强效的细胞介导免疫以及病毒中和抗体滴度。此处呈现的数据表明,用CoVaccine HT™进行佐剂接种可迅速诱导针对SARS-CoV-2的全面保护性免疫反应。