Department of Pharmacology, Dr. A.P.J Abdul Kalam University, Indore (M.P.) India - 452016.
Kota College of Pharmacy, Kota, Rajasthan- India- 324005.
Comb Chem High Throughput Screen. 2022;25(14):2391-2397. doi: 10.2174/1386207325666220315115953.
The present review covers the list of approved vaccines available in India, i.e., Covaxin, Covishield, and Sputnik-V. Covaxin's code name is BBV152. Covaxin was prepared by Hyderabad- based Bharat Biotech International Ltd. in collaboration with the National Institute of Virology (NIV) and ICMR. The effectiveness of Covaxin was found to be 78-81%. Covishield, which is available by code name AZD1222, was developed by the SII, Oxford University, and AstraZeneca. Covishield's effectiveness was found to be 90%. The time gap between the two doses of Covaxin and Covishiled is 4-6 weeks and 12-16 weeks, respectively. One more vaccine, i.e., Sputnik V, by the code name rAd26-S and rAd5-S, was developed by Gamaleya Research Institute of Epidemiology and Microbiology, which involves an interval gap of 21 days between the two doses. Covaxin releases Anti-SARS-CoV-2 IgG, which is specific to RBD (receptor-binding domain) protein, whereas a high degree of antibody response dissipates on the 28th day of vaccination. The protective efficacy of Sputnik-V was found to be ±92.2% (95% CI ±82.6-92.3), while that of Covishield was found to be ±90 % (95% CI 68.2-98.0±, p = 0.01) 2-standard dose: (61.2%, 95% CI 42.2-76.1±). In the case of Covaxin, the rate of seroconversion was found to be 93.9% (95% CI 85.2-98.2) in the 3-μg group and 97.2% (95% CI 93.1-105.1) in the 6-μg group. No significant difference was observed in local or systemic adverse reactions of the vaccine in the groups of 3 μg and 6 μg. The protective efficacious dose of Covaxin has not yet been identified. The cellular response median SFCs PBPMC of Covishield at the standard dose in the age group of 18-55 years was found to be±1201; 55-70 years: ±758 and ≥75 years: ±975. No significant increase was observed in the per million peripheral mononuclear cells (PBPMC) after administration of the booster dose of Covishield vaccine (p = 0.45 in paired student's t-test on the 28th day vs. the 42nd day). The cellular response to Sputnik V was found to be 100%. Higher levels of T cells CD8+, CD4+ T cells, and IFN- γ secretion were reported in all volunteers who had undergone vaccination. Cell proliferation was found as follows: CD: +1.5% and CD : +1.3% in the lyophilized formulation and CD4+ : + 2.6% and CD8+ : +1.5% in the frozen formulation. Antigen-specific IgG geometric mean titer (GMT) levels of Covishield were found to be highest on the 28th day with 160 geometric mean ELISA units (GMEU).
目前的综述涵盖了在印度获得批准的疫苗清单,即 Covaxin、Covishield 和 Sputnik-V。Covaxin 的代号为 BBV152。Covaxin 由海得拉巴的 Bharat Biotech International Ltd. 与国家病毒学研究所 (NIV) 和印度医学研究理事会合作研制。Covaxin 的有效性被发现为 78-81%。Covishield 的商品名为 AZD1222,由血清研究所、牛津大学和阿斯利康联合开发。Covishield 的有效性被发现为 90%。Covaxin 和 Covishield 两剂之间的时间间隔分别为 4-6 周和 12-16 周。另一种疫苗,即代号为 rAd26-S 和 rAd5-S 的 Sputnik V,由加马列亚流行病学和微生物学研究所开发,两剂之间的间隔为 21 天。Covaxin 释放针对 SARS-CoV-2 IgG 的抗体,该抗体针对 RBD(受体结合域)蛋白具有特异性,而在接种第 28 天,抗体反应的程度会下降。Sputnik-V 的保护效力被发现为±92.2%(95%置信区间±82.6-92.3),而 Covishield 的保护效力被发现为±90%(95%置信区间 68.2-98.0±,p=0.01)2 标准剂量:(61.2%,95%置信区间 42.2-76.1±)。在 Covaxin 方面,在 3-μg 组中血清转化率为 93.9%(95%置信区间 85.2-98.2),在 6-μg 组中为 97.2%(95%置信区间 93.1-105.1)。在 3μg 和 6μg 组中,疫苗的局部或全身不良反应无显著差异。Covaxin 的保护有效剂量尚未确定。在 18-55 岁年龄组中,Covishield 的标准剂量下的细胞反应中位数 PBPMC 为±1201;55-70 岁:±758 和≥70 岁:±975。在第 28 天和第 42 天进行 Covishield 疫苗加强剂量后,未观察到外周血单个核细胞(PBPMC)每百万增加(配对学生 t 检验,p=0.45)。对 Sputnik V 的细胞反应被发现为 100%。所有接受过疫苗接种的志愿者均报告了更高水平的 T 细胞 CD8+、CD4+T 细胞和 IFN-γ 分泌。细胞增殖如下:在冻干制剂中为 CD:+1.5%和 CD:+1.3%,在冷冻制剂中为 CD4+:+2.6%和 CD8+:+1.5%。Covishield 的抗原特异性 IgG 几何平均滴度(GMT)在第 28 天最高,为 160 个几何平均 ELISA 单位(GMEU)。