SARS-CoV-2 Naturally Acquired Immunity vs. Vaccine-induced Immunity, Reinfections versus Breakthrough Infections: a Retrospective Cohort Study.

S. Gazit, R. Shlezinger, G. Perez, Roni Lotan, A. Peretz, A. Ben-Tov, E. Herzel, H. Alapi, D. Cohen, K. Muhsen, G. Chodick, T. Patalon
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引用次数: 76

Abstract

BACKGROUND Waning of protection against infection with SARS-CoV-2 conferred by 2 doses of the BNT162b2 vaccine begins shortly after inoculation and becomes substantial within four months. With that, the impact of prior infection on incident SARS-CoV-2 reinfection is unclear. Therefore, we examined the long-term protection of naturally acquired immunity (protection conferred by previous infection) compared to vaccine-induced immunity. METHODS A retrospective observational study of 124,500 persons, compared two groups: (1) SARS-CoV-2-naïve individuals who received a two-dose regimen of the BioNTech/Pfizer mRNA BNT162b2 vaccine, and (2) previously infected individuals who have not been vaccinated. Two multivariate logistic regression models were applied, evaluating four SARS-CoV-2-related outcomes - infection, symptomatic disease (COVID-19), hospitalization and death - between June 1 to August 14, 2021, when the Delta variant was dominant in Israel. RESULTS SARS-CoV-2-naïve vaccinees had a 13.06-fold (95% CI, 8.08-21.11) increased risk for breakthrough infection with the Delta variant compared to unvaccinated-previously-infected individuals, when the first event (infection or vaccination) occurred during January and February of 2021. The increased risk was significant for symptomatic disease as well. When allowing the infection to occur at any time between March 2020 to February 2021, evidence of waning naturally acquired immunity was demonstrated, though SARS-CoV-2 naïve vaccinees still had a 5.96-fold (95% CI, 4.85-7.33) increased risk for breakthrough infection and a 7.13-fold (95% CI, 5.51-9.21) increased risk for symptomatic disease. CONCLUSIONS Naturally acquired immunity confers stronger protection against infection and symptomatic disease caused by the Delta variant of SARS-CoV-2, compared to the BNT162b2 two-dose vaccine-induced immunity.
SARS-CoV-2自然获得性免疫与疫苗诱导免疫、再感染与突破性感染:一项回顾性队列研究
背景:2剂BNT162b2疫苗对SARS-CoV-2感染的保护作用在接种后不久开始减弱,并在4个月内变得明显。因此,既往感染对SARS-CoV-2再感染的影响尚不清楚。因此,我们比较了自然获得性免疫与疫苗诱导免疫的长期保护作用(由既往感染产生的保护作用)。方法回顾性观察研究124,500人,比较两组:(1)SARS-CoV-2-naïve接受双剂量BioNTech/Pfizer mRNA BNT162b2疫苗方案的个体,(2)先前未接种疫苗的感染个体。应用了两个多变量logistic回归模型,评估了2021年6月1日至8月14日期间与sars - cov -2相关的四种结局——感染、症状性疾病(COVID-19)、住院和死亡,当时Delta变体在以色列占主导地位。当第一次事件(感染或接种)发生在2021年1月和2月期间时,RESULTSSARS-CoV-2-naïve疫苗接种者与未接种疫苗的先前感染个体相比,突破性感染Delta变体的风险增加了13.06倍(95% CI, 8.08-21.11)。对于有症状的疾病,增加的风险也很显著。当允许感染在2020年3月至2021年2月之间的任何时间发生时,证明了自然获得性免疫力减弱的证据,尽管SARS-CoV-2 naïve疫苗接种者发生突破性感染的风险仍增加5.96倍(95% CI, 4.85-7.33),出现症状性疾病的风险仍增加7.13倍(95% CI, 5.51-9.21)。结论与BNT162b2双剂量疫苗诱导的免疫相比,自然获得性免疫对δ型SARS-CoV-2感染和症状性疾病具有更强的保护作用。
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