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既往新冠病毒感染与疫苗接种后突破性感染风险的关联:伊朗伊斯法罕的一项队列研究

Association of Prior COVID-19 Infection with Risk of Breakthrough Infection Following Vaccination: A Cohort Study in Isfahan, Iran.

作者信息

Manteghinejad Amirreza, Rasti Sina, Nasirian Maryam, Javanmard Shaghayegh Haghjooy

机构信息

Cancer Prevention Research Center, Omid Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.

Craniofacial and Cleft Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Int J Prev Med. 2024 Jul 17;15:18. doi: 10.4103/ijpvm.ijpvm_173_23. eCollection 2024.

Abstract

BACKGROUND

Many people worldwide have developed a combination of natural and vaccine-induced immunity to COVID-19. This study investigated whether exposure to SARS-CoV-2 before full vaccination promotes protection against a breakthrough infection.

METHODS

We studied a total of 2,902,545 people in the Isfahan COVID-19 Registry. All the participants had received two doses of either Sinopharm BIBP, ChAdOx1-nCoV-19, Gam-COVID-Vac, or BIV1-CovIran vaccines. A cohort study examined the association between prior COVID-19 infection and the risk of a breakthrough infection for each vaccine. Cohorts in each pair were matched by gender, age group, calendar week of the first dose, the interval between the first and second doses, and the proportion of healthcare workers. The probable virus variant for the previous infections was also considered. Each individual's follow-up started 14 days after their second vaccine dose until either the end of the study censoring date, occurrence of a COVID-19 infection, or death. The breakthrough infection risk was compared between each cohort pair by using the hazard ratio (HR) and incidence rate ratio (IRR).

RESULTS

Total breakthrough HRs (95% confidence interval) (previously infected over infection-naïve matched cohort) were 0.36 (0.23-0.55), 0.35 (0.32-0.40), 0.37 (0.30-0.46), and 0.43 (0.32-0.56) for the BIV1-CovIran, Sinopharm BIBP, Gam-COVID-Vac, and ChAdOx1-nCoV-19 vaccine groups, respectively. The breakthrough infection IRRs were approximately similar to the total HRs mentioned above.

CONCLUSION

Prior SARS-CoV-2 infection conferred additive immunity against breakthrough after vaccination, no matter which vaccine brand was injected. Such a result could guide health authorities to codify low-cost high-benefit vaccination protocols and protect the community's well-being.

摘要

背景

全球许多人已形成对新冠病毒的自然免疫和疫苗诱导免疫的组合。本研究调查了在全程接种疫苗前接触严重急性呼吸综合征冠状病毒2(SARS-CoV-2)是否能增强对突破性感染的防护。

方法

我们对伊斯法罕新冠病毒登记处的2902545人进行了研究。所有参与者均接种了两剂国药集团北京生物制品研究所(Sinopharm BIBP)、牛津大学/阿斯利康(ChAdOx1-nCoV-19)、卫星V(Gam-COVID-Vac)或科维福(BIV1-CovIran)疫苗中的一种。一项队列研究考察了既往新冠病毒感染与每种疫苗突破性感染风险之间的关联。每对队列按性别、年龄组、第一剂接种的日历周、第一剂和第二剂之间的间隔以及医护人员比例进行匹配。还考虑了既往感染可能的病毒变体。每个人的随访从第二剂疫苗接种14天后开始,直至研究审查日期结束、出现新冠病毒感染或死亡。通过使用风险比(HR)和发病率比(IRR)比较每对队列之间的突破性感染风险。

结果

对于科维福、国药集团北京生物制品研究所、卫星V和牛津大学/阿斯利康疫苗组,总的突破性HR(95%置信区间)(既往感染组与未感染的匹配队列相比)分别为0.36(0.23 - 0.55)、0.35(0.32 - 0.40)、0.37(0.30 - 0.46)和0.43(0.32 - 0.56)。突破性感染IRR与上述总的HR大致相似。

结论

既往SARS-CoV-2感染在接种疫苗后可提供额外的针对突破性感染的免疫力,无论接种的是哪种疫苗品牌。这一结果可指导卫生当局制定低成本高效益的疫苗接种方案,保护社区健康。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b72b/11338365/149460488bc7/IJPVM-15-18-g001.jpg

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