Incidence of COVID-19 mRNA vaccine symptomatic breakthrough infections during Omicron circulation in adults with or without infection prior to vaccination

IF 2.9 4区 医学 Q2 INFECTIOUS DISEASES Infectious diseases now Pub Date : 2024-03-16 DOI:10.1016/j.idnow.2024.104886
Christine Durier , Laetitia Ninove , Sylvie van der Werf , Maeva Lefebvre , Corinne Desaint , Rebecca Bauer , Mikael Attia , Anne-Sophie Lecompte , Marie Lachatre , Zoha Maakaroun-Vermesse , Jean-François Nicolas , Renaud Verdon , Jean-Jacques Kiladjian , Paul Loubet , Catherine Schmidt-Mutter , Violaine Corbin , Séverine Ansart , Giovanna Melica , Martine Resch , Emmanuelle Netzer , Odile Launay
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Abstract

Objectives

COVID-19 vaccine breakthrough infections were frequently reported during circulation of the Omicron variant. The ANRS|MIE CoviCompareP study investigated these infections in adults vaccinated and boosted with BNT162b2 [Pfizer-BioNTech] and with/without SARS-CoV-2 infection before vaccination.

Methods

In the first half of 2021, healthy adults (aged 18–45, 65–74 and 75 or older) received either one dose of BNT162b2 (n = 120) if they had a documented history of SARS-CoV-2 infection at least five months previously, or two doses (n = 147) if they had no history confirmed by negative serological tests. A first booster dose was administered at least 6 months after the primary vaccination, and a second booster dose, if any, was reported in the database. Neutralizing antibodies (NAbs) against the European (D614G) strain and the Omicron BA.1 variant were assessed up to 28 days after the first booster dose. A case-control analysis was performed for the 252 participants who were followed up in 2022, during the Omicron waves.

Results

From January to October 2022, 78/252 (31%) had a documented symptomatic breakthrough infection after full vaccination: 21/117 (18%) in those who had been infected before vaccination vs. 57/135 (42%) in those who had not. In a multivariate logistic regression model, factors associated with a lower risk of breakthrough infection were older age, a higher number of booster doses, and higher levels of Omicron BA.1 NAb titers in adults with infection before vaccination, but not in those without prior infection.

Conclusion

Our results highlight the need to consider immune markers of protection in association with infection and vaccination history.

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在 Omicron 循环期间,接种疫苗前感染或未感染 COVID-19 mRNA 疫苗的成人出现无症状突破性感染的发生率。
目标:在 Omicron 变体的流通过程中,经常有 COVID-19 疫苗突破性感染的报道。ANRS|MIE CoviCompareP 研究调查了接种 BNT162b2 [Pfizer-BioNTech] 疫苗和强化接种 BNT162b2 [Pfizer-BioNTech] 的成人以及接种前感染/未感染 SARS-CoV-2 的成人的感染情况:2021 年上半年,健康成年人(年龄在 18-45 岁、65-74 岁和 75 岁或以上)如果至少在五个月前有 SARS-CoV-2 感染病史记录,则接种一剂 BNT162b2(n = 120);如果经血清学检测阴性证实无感染病史,则接种两剂(n = 147)。第一次加强免疫至少在第一次接种后 6 个月进行,如果有第二次加强免疫,则在数据库中报告。针对欧洲(D614G)毒株和 Omicron BA.1 变异株的中和抗体(NAbs)在第一次加强接种后 28 天内进行了评估。对 2022 年欧米克隆波期间接受随访的 252 名参与者进行了病例对照分析:从 2022 年 1 月到 10 月,78/252(31%)人在接种全部疫苗后出现了有记录的症状性突破感染:接种疫苗前已感染者为 21/117(18%),未感染者为 57/135(42%)。在一个多变量逻辑回归模型中,与突破性感染风险较低相关的因素有:年龄较大、加强接种次数较多、接种前曾感染的成人的 Omicron BA.1 NAb 滴度水平较高,而未感染过的成人则没有:我们的研究结果凸显了考虑免疫保护标志物与感染和疫苗接种史相关性的必要性。
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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来源期刊
Infectious diseases now
Infectious diseases now Medicine-Infectious Diseases
CiteScore
7.10
自引率
2.90%
发文量
116
审稿时长
40 days
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