CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunogenicity and protective efficacy of SARS-CoV-2 recombinant S-protein vaccine S-268019-b in cynomolgus monkeys.
Immunogenicity and protective efficacy of SARS-CoV-2 recombinant S-protein vaccine S-268019-b in cynomolgus monkeys.
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疫苗 S-268019-b 是一种严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突(S)蛋白疫苗,由全长重组 SARS-CoV-2 S 蛋白(S-910823)作为抗原,与基于角鲨烯的佐剂 A-910823 混合而成。
本研究评估了使用不同剂量 S-910823 的 S-268019-b 的免疫原性,以及其在食蟹猴中对 SARS-CoV-2 攻击的疫苗效力。不同剂量的 S-910823 联合 A-910823 以 3 周间隔肌肉注射两次。第二次给药后两周,观察到剂量依赖性体液免疫反应,其中和抗体滴度与人恢复期血浆相当。与针对祖先病毒相比,携带 Beta 和 Gamma SARS-CoV-2 变异株 S 蛋白的假病毒对两剂疫苗后诱导的中和抗体敏感性约降低 3 至 4 倍,而针对 Omicron 变异株的中和抗体滴度降低 >14 倍。细胞免疫也被诱导,并呈现相对 Th1 偏倚的反应。未观察到与疫苗相关的不良临床体征或体重减轻,提示该疫苗在食蟹猴中的安全性。根据鼻咽、咽和直肠拭子标本中的基因组和亚基因组病毒 RNA 转录水平,使用 10 µg S-910823 联合 A-910823 免疫显示出对 SARS-CoV-2 攻击的保护效力。病理分析显示,在受到攻击的接种疫苗猴肺中未检测到疫苗依赖性疾病增强。当前研究结果为人体试验中的疫苗剂量提供了基础信息,并支持将S-268019-b开发为一种安全有效的疫苗,用于控制当前疫情以及未来对SARS-CoV-2的普遍防护。
The vaccine S-268019-b is a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike (S)-protein vaccine consisting of full-length recombinant SARS-CoV-2 S-protein (S-910823) as antigen, mixed with the squalene-based adjuvant A-910823. The current study evaluated the immunogenicity of S-268019-b using various doses of S-910823 and its vaccine efficacy against SARS-CoV-2 challenge in cynomolgus monkeys. The different doses of S-910823 combined with A-910823 were intramuscularly administered twice at a 3-week interval. Two weeks after the second dosing, dose-dependent humoral immune responses were observed with neutralizing antibody titers being comparable to that of human convalescent plasma. Pseudoviruses harboring S proteins from Beta and Gamma SARS-CoV-2 variants displayed approximately 3- to 4-fold reduced sensitivity to neutralizing antibodies induced after two vaccine doses compared with that against ancestral viruses, whereas neutralizing antibody titers were reduced >14-fold against the Omicron variant.
Cellular immunity was also induced with a relative Th1 polarized response. No adverse clinical signs or weight loss associated with the vaccine were observed, suggesting safety of the vaccine in cynomolgus monkeys. Immunization with 10 µg of S-910823 with A-910823 demonstrated protective efficacy against SARS-CoV-2 challenge according to genomic and subgenomic viral RNA transcript levels in nasopharyngeal, throat, and rectal swab specimens.
Pathological analysis revealed no detectable vaccine-dependent enhancement of disease in the lungs of challenged vaccinated monkeys. The current findings provide fundamental information regarding vaccine doses for human trials and support the development of S-268019-b as a safe and effective vaccine for controlling the current pandemic, as well as general protection against SARS-CoV-2 moving forward.
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