Homologous equivalence study of immunogenicity after third dose of Covid-19 vaccine (recombinant) with an interval of six months after the second dose, comparing the interval of eight and 12 weeks between the first two doses.

Clarice Monteiro Vianna,Gloria Regina da Silva E Sá,Maria Vitória Hadland Seid,Luiz Antonio Bastos Camacho,Janaína Reis Xavier,Vitor Cardoso da Gama,Thalita da Matta de Castro,Ewerton Alves Portela Dos Santos,Camila Dias de Almeida,Robson Leite de Souza Cruz,Marilda Siqueira,Maria de Lourdes de Sousa Maia,Clara Lucy de Vasconcellos Ferroco,Mia Ferreira de Araújo,Luis Fernando López Tort,Braulia Costa Caetano
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Abstract

BACKGROUND In response to the coronavirus disease 2019 (Covid-19) pandemic, Brazil authorised the Astra Zeneca/Fiocruz vaccine in January 2021. As the Delta variant emerged in May 2021, interval between vaccine doses was adjusted. By September 2021, the Brazilian National Immunisation Program recommended a booster dose for individuals over 70, and later expanded the recommendation to all adults. OBJECTIVES Assess the equivalence of IgG antibody response against the Covid-19 S protein before and approximately 28 days after the third dose of a Covid-19 recombinant vaccine. Two groups received initial two doses with intervals of eight and 12 weeks. METHODS This is a phase IV clinical study, uncontrolled, non-randomised. The study proposes calculating the ratio of geometric means titres (GMT) 28 days after the third dose, with a target ratio of confidence interval (CI) between 0.77 and 1.3. FINDINGS In the primary endpoint, there was no equivalence between the eight- and 12-week intervals with a slight variation favouring the eight-week group. Post-third dose, both groups showed increases titres at 28 days, three months, six months and 12 months. Both groups responded similarly to Delta and Omicron BA.1, with a more significant increase for Delta. MAIN CONCLUSIONS The study showed strong and consistent immune response in all age groups receiving the Covid-19 recombinant vaccine. Third dose elicited an increase in GMT by at least three times aligned with Ministry of Health strategies emphasising Bio-Manguinhos crucial role in pandemic control in the country.
比较前两剂疫苗之间 8 周和 12 周的间隔时间,进行 Covid-19 疫苗(重组)第三剂后间隔 6 个月的免疫原性同源等效性研究。
背景为应对2019年冠状病毒病(Covid-19)大流行,巴西于2021年1月授权使用阿斯利康/菲克鲁兹疫苗。由于2021年5月出现了Delta变种,疫苗接种的间隔时间进行了调整。到 2021 年 9 月,巴西国家免疫计划建议 70 岁以上的人接种加强剂,后来又将该建议扩大到所有成年人。目的评估在接种第三剂 Covid-19 重组疫苗之前和之后约 28 天内针对 Covid-19 S 蛋白的 IgG 抗体反应的等效性。两组分别接种最初的两剂疫苗,间隔时间分别为 8 周和 12 周。方法这是一项 IV 期临床研究,非对照、非随机。研究建议计算第三剂后 28 天的几何平均滴度(GMT)比值,目标比值的置信区间(CI)在 0.77 和 1.3 之间。研究结果在主要终点上,8 周和 12 周间隔之间不存在等效性,8 周组略有差异。第三次用药后,两组在 28 天、3 个月、6 个月和 12 个月的滴度均有所上升。两组对 Delta 和 Omicron BA.1 的反应相似,Delta 的上升更为显著。根据卫生部强调 Bio-Manguinhos 在该国大流行病控制中的关键作用的战略,第三剂疫苗可使 GMT 至少提高三倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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