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先前 SARS-CoV-2 感染、COVID-19 加强针和混合免疫对奥密克戎重症的保护作用:加拿大五百万居民的基于人群的队列研究。

Protection of prior SARS-CoV-2 infection, COVID-19 boosters, and hybrid immunity against Omicron severe illness: A population-based cohort study of five million residents in Canada.

机构信息

Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.

Department of Epidemiology, Johns Hopkins University, Baltimore, Maryland, United States of America.

出版信息

PLoS One. 2024 Feb 23;19(2):e0299304. doi: 10.1371/journal.pone.0299304. eCollection 2024.

Abstract

BACKGROUND

Evidence on protection of different patterns of infection- and vaccine-acquired immunity against Omicron-associated severe illness is useful in planning booster vaccination strategies. We examined protection of prior SARS-CoV-2 infection, a third or a fourth COVID-19 vaccine dose, and hybrid immunity against Omicron-associated severe illness.

METHODS AND FINDINGS

This population-based cohort study followed five million individuals with at least one SARS-CoV-2 RT-PCR test before November 21, 2021 until an Omicron-associatedhospitalization or death. We used Cox regression models to estimate risks of Omicron-associated hospitalization and a composite severe outcome (hospitalized and death), among individuals with infection- and/or vaccination-acquired immunity. Individuals who were unvaccinated and had no history of a prior infection severed as the reference group. Both adjusted hazard ratios (HR) and corresponding protection (one minus adjusted HR), with 95% confidence intervals (CIs), were reported. Three doses provided 94% (95%CI 93-95) and 93% (95%CI 91-94) protection against Omicron-associated hospitalization at 2-3 and ≥3 months post-vaccination respectively, similar to the protection conferred by three doses and a prior infection (2-3 months: 99%, 95%CI 97-100; ≥3 months: 97%, 95%CI 92-99) and four doses (1 month: 87%, 95%CI 79-92; 1-2 months: 96%, 95%CI 92-98). In individuals ≥65 years old, protection of four doses increased to 95% (95%CI 91-98) at 1-2 months, significantly higher than that of three doses over the follow-up period. Similar results were observed with the composite severe outcome.

CONCLUSION

At least three antigenic exposures, achieved by vaccination or infection, confers significant protection against Omicron-associated hospitalization and death in all age groups. Our findings support a third dose for the overall population, regardless of prior infection status, and a fourth dose for the elderly to maintain high level of immunity and substantially reduce risk of severe illness at individual level.

摘要

背景

针对奥密克戎相关重症,不同模式的感染和疫苗获得性免疫的保护作用的相关证据,对于制定加强针接种策略很有帮助。本研究旨在评估既往 SARS-CoV-2 感染、第三或第四剂 COVID-19 疫苗接种以及混合免疫对奥密克戎相关重症的保护作用。

方法和发现

本基于人群的队列研究纳入了 2021 年 11 月 21 日之前至少接受过一次 SARS-CoV-2 RT-PCR 检测的 500 万名个体,随访终点为奥密克戎相关住院或死亡。我们使用 Cox 回归模型来估计具有感染和/或疫苗获得性免疫个体的奥密克戎相关住院和复合严重结局(住院和死亡)的风险。未接种疫苗且无既往感染史的个体作为参照组。报告了调整后的风险比(HR)和相应的保护率(调整后 HR 的 1 减数值,95%置信区间(CI))。第三剂疫苗在接种后 2-3 个月和≥3 个月时,对奥密克戎相关住院的保护率分别为 94%(95%CI 93-95)和 93%(95%CI 91-94),与第三剂疫苗和既往感染(2-3 个月:99%,95%CI 97-100;≥3 个月:97%,95%CI 92-99)和第四剂疫苗(1 个月:87%,95%CI 79-92;1-2 个月:96%,95%CI 92-98)的保护作用相似。在≥65 岁的个体中,第四剂疫苗在 1-2 个月时的保护率增加到 95%(95%CI 91-98),显著高于整个随访期间第三剂疫苗的保护率。对于复合严重结局,也观察到了类似的结果。

结论

在所有年龄段,至少三次抗原暴露(通过接种或感染获得)可显著降低奥密克戎相关住院和死亡的风险。本研究结果支持在全人群中接种第三剂疫苗,无论既往感染状态如何,以及为了在个体层面保持高水平免疫并显著降低重症风险,为老年人接种第四剂疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ddd/10889649/cba082715fd5/pone.0299304.g001.jpg

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