Ganneru Brunda, Jogdand Harsh, Daram Vijaya Kumar, Das Dipankar, Molugu Narasimha Reddy, Prasad Sai D, Kannappa Srinivas V, Ella Krishna M, Ravikrishnan Rajaram, Awasthi Amit, Jose Jomy, Rao Panduranga, Kumar Deepak, Ella Raches, Abraham Priya, Yadav Pragya D, Sapkal Gajanan N, Shete-Aich Anita, Desphande Gururaj, Mohandas Sreelekshmy, Basu Atanu, Gupta Nivedita, Vadrevu Krishna Mohan
Bharat Biotech International Ltd, Hyderabad (BBIL), Telangana 500 078, India.
RCC Laboratories India Private Ltd, Hyderabad, Telangana 500 078, India.
iScience. 2021 Apr 23;24(4):102298. doi: 10.1016/j.isci.2021.102298. Epub 2021 Mar 10.
We report the development and evaluation of safety and immunogenicity of a whole virion inactivated (WVI) SARS-CoV-2 vaccine (BBV152), adjuvanted with aluminum hydroxide gel (Algel), or TLR7/8 agonist chemisorbed Algel. We used a well-characterized SARS-CoV-2 strain and an established Vero cell platform to produce large-scale GMP-grade highly purified inactivated antigen. Product development and manufacturing process were carried out in a BSL-3 facility. Immunogenicity and safety were determined at two antigen concentrations (3μg and 6μg), with two different adjuvants, in mice, rats, and rabbits. Our results show that BBV152 vaccine formulations generated significantly high antigen-binding and neutralizing antibody titers (NAb), at both concentrations, in all three species with excellent safety profiles. The inactivated vaccine formulation contains TLR7/8 agonist adjuvant-induced Th1-biased antibody responses with elevated IgG2a/IgG1 ratio and increased levels of SARS-CoV-2-specific IFN-γ CD4 T lymphocyte response. Our results support further development for phase I/II clinical trials in humans.
我们报告了一种全病毒灭活(WVI)的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗(BBV152)的研发以及安全性和免疫原性评估,该疫苗佐以氢氧化铝凝胶(Algel)或经Toll样受体7/8(TLR7/8)激动剂化学吸附的Algel。我们使用了一种特征明确的SARS-CoV-2毒株和一个成熟的非洲绿猴肾(Vero)细胞平台来大规模生产符合药品生产质量管理规范(GMP)级别的高度纯化的灭活抗原。产品研发和生产过程在生物安全三级(BSL-3)设施中进行。在小鼠、大鼠和兔子中,以两种不同佐剂、两种抗原浓度(3μg和6μg)测定免疫原性和安全性。我们的结果表明,BBV152疫苗制剂在所有三个物种中,于两种浓度下均产生了显著高的抗原结合和中和抗体滴度(NAb),且安全性良好。该灭活疫苗制剂含有TLR7/8激动剂佐剂诱导的以Th1为主的抗体反应,IgG2a/IgG1比值升高,且严重急性呼吸综合征冠状病毒2特异性干扰素-γ CD4 T淋巴细胞反应水平增加。我们的结果支持进一步开展针对人类的I/II期临床试验。