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卡塔尔既往感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)与mRNA疫苗接种后突破性感染风险的关联

Association of Prior SARS-CoV-2 Infection With Risk of Breakthrough Infection Following mRNA Vaccination in Qatar.

作者信息

Abu-Raddad Laith J, Chemaitelly Hiam, Ayoub Houssein H, Yassine Hadi M, Benslimane Fatiha M, Al Khatib Hebah A, Tang Patrick, Hasan Mohammad R, Coyle Peter, Al Kanaani Zaina, Al Kuwari Einas, Jeremijenko Andrew, Kaleeckal Anvar Hassan, Latif Ali Nizar, Shaik Riyazuddin Mohammad, Abdul Rahim Hanan F, Nasrallah Gheyath K, Al Kuwari Mohamed Ghaith, Butt Adeel A, Al Romaihi Hamad Eid, Al-Thani Mohamed H, Al Khal Abdullatif, Bertollini Roberto

机构信息

Infectious Disease Epidemiology Group, Weill Cornell Medicine-Qatar, Cornell University, Doha, Qatar.

World Health Organization Collaborating Centre for Disease Epidemiology Analytics on HIV/AIDS, Sexually Transmitted Infections, and Viral Hepatitis, Weill Cornell Medicine-Qatar, Cornell University, Qatar Foundation-Education City, Doha, Qatar.

出版信息

JAMA. 2021 Nov 16;326(19):1930-1939. doi: 10.1001/jama.2021.19623.

Abstract

IMPORTANCE

The effect of prior SARS-CoV-2 infection on vaccine protection remains poorly understood.

OBJECTIVE

To assess protection from SARS-CoV-2 breakthrough infection after mRNA vaccination among persons with vs without prior SARS-CoV-2 infection.

DESIGN, SETTING, AND PARTICIPANTS: Matched-cohort studies in Qatar for the BNT162b2 (Pfizer-BioNTech) and mRNA-1273 (Moderna) vaccines. A total of 1 531 736 individuals vaccinated with either vaccine between December 21, 2020, and September 19, 2021, were followed up beginning 14 days after receiving the second dose until September 19, 2021.

EXPOSURES

Prior SARS-CoV-2 infection and COVID-19 vaccination.

MAIN OUTCOMES AND MEASURES

Incident SARS-CoV-2 infection, defined as a polymerase chain reaction (PCR)-positive nasopharyngeal swab regardless of reason for PCR testing or presence of symptoms. Cumulative incidence was calculated using the Kaplan-Meier estimator method.

RESULTS

The BNT162b2-vaccinated cohort comprised 99 226 individuals with and 290 432 matched individuals without prior PCR-confirmed infection (median age, 37 years; 68% male). The mRNA-1273-vaccinated cohort comprised 58 096 individuals with and 169 514 matched individuals without prior PCR-confirmed infection (median age, 36 years; 73% male). Among BNT162b2-vaccinated persons, 159 reinfections occurred in those with and 2509 in those without prior infection 14 days or more after dose 2. Among mRNA-1273-vaccinated persons, 43 reinfections occurred in those with and 368 infections in those without prior infection. Cumulative infection incidence among BNT162b2-vaccinated individuals was an estimated 0.15% (95% CI, 0.12%-0.18%) in those with and 0.83% (95% CI, 0.79%-0.87%) in those without prior infection at 120 days of follow-up (adjusted hazard ratio for breakthrough infection with prior infection, 0.18 [95% CI, 0.15-0.21]; P < .001). Cumulative infection incidence among mRNA-1273-vaccinated individuals was an estimated 0.11% (95% CI, 0.08%-0.15%) in those with and 0.35% (95% CI, 0.32%-0.40%) in those without prior infection at 120 days of follow-up (adjusted hazard ratio, 0.35 [95% CI, 0.25-0.48]; P < .001). Vaccinated individuals with prior infection 6 months or more before dose 1 had statistically significantly lower risk for breakthrough infection than those vaccinated less than 6 months before dose 1 (adjusted hazard ratio, 0.62 [95% CI, 0.42-0.92]; P = .02 for BNT162b2 and 0.40 [95% CI, 0.18-0.91]; P = .03 for mRNA-1273 vaccination).

CONCLUSIONS AND RELEVANCE

Prior SARS-CoV-2 infection was associated with a statistically significantly lower risk for breakthrough infection among individuals receiving the BNT162b2 or mRNA-1273 vaccines in Qatar between December 21, 2020, and September 19, 2021. The observational study design precludes direct comparisons of infection risk between the 2 vaccines.

摘要

重要性

既往感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)对疫苗保护效果的影响仍知之甚少。

目的

评估既往感染过SARS-CoV-2与未感染过SARS-CoV-2的人群在接种mRNA疫苗后预防SARS-CoV-2突破性感染的情况。

设计、地点和参与者:在卡塔尔进行的针对BNT162b2(辉瑞-生物科技)和mRNA-1273(莫德纳)疫苗的匹配队列研究。2020年12月21日至2021年9月19日期间接种这两种疫苗的1531736名个体,在接种第二剂疫苗14天后开始随访,直至2021年9月19日。

暴露因素

既往SARS-CoV-2感染和新冠病毒疫苗接种。

主要结局和测量指标

SARS-CoV-2感染事件,定义为无论聚合酶链反应(PCR)检测原因或是否有症状,鼻咽拭子PCR检测呈阳性。使用Kaplan-Meier估计法计算累积发病率。

结果

接种BNT162b2疫苗的队列包括99226名既往有PCR确诊感染的个体和290432名匹配的无既往感染个体(中位年龄37岁;68%为男性)。接种mRNA-1273疫苗的队列包括58096名既往有PCR确诊感染的个体和169514名匹配的无既往感染个体(中位年龄36岁;73%为男性)。在接种BNT162b2疫苗的人群中,既往有感染的个体在第2剂接种14天或更久后有159例再次感染,无既往感染的个体有2509例感染。在接种mRNA-1273疫苗的人群中,既往有感染的个体有43例再次感染,无既往感染的个体有368例感染。在随访120天时,接种BNT162b2疫苗的个体中,既往有感染的累积感染发病率估计为0.15%(95%CI,0.12%-0.18%),无既往感染的为0.83%(95%CI,0.79%-0.87%)(既往感染的突破性感染调整风险比,0.18[95%CI,0.15-0.21];P<0.001)。在随访120天时,接种mRNA-1273疫苗的个体中,既往有感染的累积感染发病率估计为0.11%(95%CI,0.08%-0.15%),无既往感染的为0.35%(95%CI,0.32%-0.40%)(调整风险比,0.35[95%CI,0.25-0.48];P<0.001)。在第1剂接种前6个月或更久前有既往感染的接种个体,其突破性感染风险在统计学上显著低于第1剂接种前不到6个月接种的个体(BNT162b2疫苗的调整风险比,0.62[95%CI,0.42-0.92];P=0.02;mRNA-1273疫苗的调整风险比,0.40[95%CI,0.18-0.91];P=0.03)。

结论与意义

在2020年12月21日至2021年9月19日期间的卡塔尔,既往SARS-CoV-2感染与接受BNT162b2或mRNA-1273疫苗的个体中突破性感染风险在统计学上显著降低相关。观察性研究设计排除了两种疫苗之间感染风险的直接比较。

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