Indian Council of Medical Research-National Institute of Virology, Pune, 411021, Maharashtra, India.
Bharat Biotech International Limited, Genome Valley, Hyderabad, 500 078, Telangana, India.
Nat Commun. 2021 Mar 2;12(1):1386. doi: 10.1038/s41467-021-21639-w.
The COVID-19 pandemic is a global health crisis that poses a great challenge to the public health system of affected countries. Safe and effective vaccines are needed to overcome this crisis. Here, we develop and assess the protective efficacy and immunogenicity of an inactivated SARS-CoV-2 vaccine in rhesus macaques. Twenty macaques were divided into four groups of five animals each. One group was administered a placebo, while three groups were immunized with three different vaccine candidates of BBV152 at 0 and 14 days. All the macaques were challenged with SARS-CoV-2 fourteen days after the second dose. The protective response was observed with increasing SARS-CoV-2 specific IgG and neutralizing antibody titers from 3-week post-immunization. Viral clearance was observed from bronchoalveolar lavage fluid, nasal swab, throat swab and lung tissues at 7 days post-infection in the vaccinated groups. No evidence of pneumonia was observed by histopathological examination in vaccinated groups, unlike the placebo group which exhibited interstitial pneumonia and localization of viral antigen in the alveolar epithelium and macrophages by immunohistochemistry. This vaccine candidate BBV152 has completed Phase I/II (NCT04471519) clinical trials in India and is presently in phase III, data of this study substantiates the immunogenicity and protective efficacy of the vaccine candidates.
新型冠状病毒肺炎疫情是一场全球性的卫生危机,对受影响国家的公共卫生系统构成了巨大挑战。需要安全有效的疫苗来克服这一危机。在这里,我们开发并评估了一种灭活的 SARS-CoV-2 疫苗在恒河猴中的保护效力和免疫原性。20 只恒河猴被分为四组,每组 5 只。一组给予安慰剂,三组分别用三种不同的 BBV152 疫苗候选物在 0 天和 14 天进行免疫。所有恒河猴在第二次给药后 14 天接受 SARS-CoV-2 挑战。从免疫后 3 周开始,观察到 SARS-CoV-2 特异性 IgG 和中和抗体滴度的增加,从而观察到保护反应。在接种组中,在感染后 7 天从支气管肺泡灌洗液、鼻拭子、咽拭子和肺组织中清除了病毒。接种组未通过组织病理学检查观察到肺炎的证据,而安慰剂组则通过免疫组织化学显示间质性肺炎和病毒抗原在肺泡上皮细胞和巨噬细胞中的定位。这种疫苗候选物 BBV152 已经在印度完成了 I/II 期(NCT04471519)临床试验,目前正在进行 III 期,本研究的数据证实了疫苗候选物的免疫原性和保护效力。