A comparative study of the effectiveness of Pfizer-BioNTech (BNT162b2), Astra Zeneca (ChAdOx1nCoV-19) and Sinopharm (BBIBP-CorV) vaccines in eliciting Humoral immunity in a sample of vaccinated population from Iraq.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Furqan Mohammed, A. Sahib
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Abstract

Background: In order to tackle COVID-19 pandemic and the emerging variants, researchers around the globe have investigated many vaccine candidates from different manufacturers, however vaccine development is not an easy task but is a top priority to restore normalcy as represented a step to achieve the desired herd immunity threshold. Patients and methods: in this study we assessed and compared the level of IgG anti-RBD neutralizing antibodies triggered from each vaccine against SARS-CoV2 infection in 123 vaccinated subjects, by using isotypeand species- free competitive blocking ELISA. Blood samples were taken from vaccinated individuals 1 and 8 months after the second dose of the vaccines. Results: the findings of the current study revealed that two-dose vaccination might be effective to trigger robust humoral neutralizing immunity at 1month and even durable for as long as 8months with different sustained levels among the three studied previously mentioned vaccines. The serum level of the neutralizing IgG antibodies, Pfizer group revealed the highest level compared to AstraZeneca and Sinopharm groups (P<0.05); the Sinopharm showed trend of higher levels of neutralizing antibodies than AstraZeneca but without reaching statistical significance (P>0.05). Additionally, the serum level of neutralizing IgG antibodies, which represent the humeral immunity to SARSCoV- 2, was shown to be far higher in 1-month than in 8-month post-2nd dose vaccination groups (P<0.0001). Conclusion: Altogether, it is concluded that Pfizer vaccine proved to be of highest and most durable neutralizing anti-RBD IgG antibodies and followed with Sinopharm and AstraZeneca vaccines. Bangladesh Journal of Medical Science Vol. 22 No. 03 July’23 Page : 553-563
辉瑞- biontech (BNT162b2)、阿斯特拉-利康(ChAdOx1nCoV-19)和国药(BBIBP-CorV)疫苗在伊拉克接种人群中激发体液免疫效果的比较研究
背景:为了应对COVID-19大流行和新出现的变体,全球研究人员已经研究了来自不同制造商的许多候选疫苗,然而疫苗开发不是一项容易的任务,而是恢复正常的首要任务,因为它代表了实现所需群体免疫阈值的一步。患者和方法:在本研究中,我们采用同种型和无种竞争性阻断ELISA法,评估和比较了123名接种疫苗的受试者中每种针对SARS-CoV2感染的疫苗触发的IgG抗rbd中和抗体水平。在接种第二剂疫苗后1个月和8个月采集了接种者的血液样本。结果:目前的研究结果表明,两剂疫苗接种可能有效地在1个月时触发强大的体液中和免疫,甚至持续长达8个月,但上述三种疫苗的持续水平不同。血清中和性IgG抗体水平,辉瑞组高于阿斯利康组和国药组(P0.05)。此外,血清中和性IgG抗体(代表肱骨对SARSCoV- 2的免疫)水平在第二次接种后1个月远高于第二次接种后8个月(P<0.0001)。结论:综上所述,辉瑞疫苗具有最高和最持久的抗rbd IgG抗体,其次是国药和阿斯利康疫苗。《孟加拉国医学科学杂志》第22卷第23年7月3日第553-563页
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来源期刊
Bangladesh Journal of Medical Science
Bangladesh Journal of Medical Science MEDICINE, GENERAL & INTERNAL-
CiteScore
1.70
自引率
55.60%
发文量
139
审稿时长
24 weeks
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