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以色列全国疫苗接种运动后,mRNA BNT162b2疫苗对SARS-CoV-2感染及COVID-19病例、住院和死亡的影响与效果:一项利用国家监测数据的观察性研究

Impact and effectiveness of mRNA BNT162b2 vaccine against SARS-CoV-2 infections and COVID-19 cases, hospitalisations, and deaths following a nationwide vaccination campaign in Israel: an observational study using national surveillance data.

作者信息

Haas Eric J, Angulo Frederick J, McLaughlin John M, Anis Emilia, Singer Shepherd R, Khan Farid, Brooks Nati, Smaja Meir, Mircus Gabriel, Pan Kaijie, Southern Jo, Swerdlow David L, Jodar Luis, Levy Yeheskel, Alroy-Preis Sharon

机构信息

Public Health Services, Israel Ministry of Health, Jerusalem, Israel; Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheva, Israel.

Pfizer, Collegeville, PA, USA.

出版信息

Lancet. 2021 May 15;397(10287):1819-1829. doi: 10.1016/S0140-6736(21)00947-8. Epub 2021 May 5.

DOI:10.1016/S0140-6736(21)00947-8
PMID:33964222
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8099315/
Abstract

BACKGROUND

Following the emergency use authorisation of the Pfizer-BioNTech mRNA COVID-19 vaccine BNT162b2 (international non-proprietary name tozinameran) in Israel, the Ministry of Health (MoH) launched a campaign to immunise the 6·5 million residents of Israel aged 16 years and older. We estimated the real-world effectiveness of two doses of BNT162b2 against a range of SARS-CoV-2 outcomes and to evaluate the nationwide public-health impact following the widespread introduction of the vaccine.

METHODS

We used national surveillance data from the first 4 months of the nationwide vaccination campaign to ascertain incident cases of laboratory-confirmed SARS-CoV-2 infections and outcomes, as well as vaccine uptake in residents of Israel aged 16 years and older. Vaccine effectiveness against SARS-CoV-2 outcomes (asymptomatic infection, symptomatic infection, and COVID-19-related hospitalisation, severe or critical hospitalisation, and death) was calculated on the basis of incidence rates in fully vaccinated individuals (defined as those for whom 7 days had passed since receiving the second dose of vaccine) compared with rates in unvaccinated individuals (who had not received any doses of the vaccine), with use of a negative binomial regression model adjusted for age group (16-24, 25-34, 35-44, 45-54, 55-64, 65-74, 75-84, and ≥85 years), sex, and calendar week. The proportion of spike gene target failures on PCR test among a nationwide convenience-sample of SARS-CoV-2-positive specimens was used to estimate the prevelance of the B.1.1.7 variant.

FINDINGS

During the analysis period (Jan 24 to April 3, 2021), there were 232 268 SARS-CoV-2 infections, 7694 COVID-19 hospitalisations, 4481 severe or critical COVID-19 hospitalisations, and 1113 COVID-19 deaths in people aged 16 years or older. By April 3, 2021, 4 714 932 (72·1%) of 6 538 911 people aged 16 years and older were fully vaccinated with two doses of BNT162b2. Adjusted estimates of vaccine effectiveness at 7 days or longer after the second dose were 95·3% (95% CI 94·9-95·7; incidence rate 91·5 per 100 000 person-days in unvaccinated vs 3·1 per 100 000 person-days in fully vaccinated individuals) against SARS-CoV-2 infection, 91·5% (90·7-92·2; 40·9 vs 1·8 per 100 000 person-days) against asymptomatic SARS-CoV-2 infection, 97·0% (96·7-97·2; 32·5 vs 0·8 per 100 000 person-days) against symptomatic COVID-19, 97·2% (96·8-97·5; 4·6 vs 0·3 per 100 000 person-days) against COVID-19-related hospitalisation, 97·5% (97·1-97·8; 2·7 vs 0·2 per 100 000 person-days) against severe or critical COVID-19-related hospitalisation, and 96·7% (96·0-97·3; 0·6 vs 0·1 per 100 000 person-days) against COVID-19-related death. In all age groups, as vaccine coverage increased, the incidence of SARS-CoV-2 outcomes declined. 8006 of 8472 samples tested showed a spike gene target failure, giving an estimated prevalence of the B.1.1.7 variant of 94·5% among SARS-CoV-2 infections.

INTERPRETATION

Two doses of BNT162b2 are highly effective across all age groups (≥16 years, including older adults aged ≥85 years) in preventing symptomatic and asymptomatic SARS-CoV-2 infections and COVID-19-related hospitalisations, severe disease, and death, including those caused by the B.1.1.7 SARS-CoV-2 variant. There were marked and sustained declines in SARS-CoV-2 incidence corresponding to increasing vaccine coverage. These findings suggest that COVID-19 vaccination can help to control the pandemic.

FUNDING

None.

摘要

背景

在辉瑞 - 生物科技公司的mRNA新冠疫苗BNT162b2(国际非专利名称为托珠单抗)在以色列获得紧急使用授权后,以色列卫生部发起了一项运动,为该国650万16岁及以上居民进行免疫接种。我们估计了两剂BNT162b2对一系列严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染结果的实际效果,并评估了该疫苗广泛接种后对全国公共卫生的影响。

方法

我们使用了全国疫苗接种运动前4个月的国家监测数据,以确定实验室确诊的SARS-CoV-2感染病例和结果,以及以色列16岁及以上居民的疫苗接种情况。根据完全接种疫苗个体(定义为自接种第二剂疫苗起已过去7天的个体)与未接种疫苗个体(未接种任何剂量疫苗的个体)的发病率,使用负二项回归模型,并对年龄组(16 - 24岁、25 - 34岁、35 - 44岁、45 - 54岁、55 - 64岁、65 - 74岁、75 - 84岁和≥85岁)、性别和日历周进行调整,计算疫苗对SARS-CoV-2感染结果(无症状感染、有症状感染以及与新冠病毒病相关的住院、重症或危重症住院和死亡)的有效性。在全国范围内对SARS-CoV-2阳性标本进行的便利抽样中,PCR检测中刺突基因靶点失败的比例用于估计B.1.1.7变异株的流行率。

结果

在分析期间(2021年1月24日至4月3日),16岁及以上人群中有232268例SARS-CoV-2感染、7694例新冠病毒病住院、4481例重症或危重症新冠病毒病住院以及1113例新冠病毒病死亡。到2021年4月3日,在6538911名16岁及以上人群中,4714932人(72.1%)完成了两剂BNT162b2的接种。第二剂接种7天或更长时间后的疫苗有效性调整估计值为:针对SARS-CoV-2感染为95.3%(95%置信区间94.9 - 95.7;未接种疫苗者每100000人日发病率为91.5,完全接种疫苗个体为每100000人日3.1),针对无症状SARS-CoV-2感染为91.5%(90.7 - 92.2;每100000人日40.9对1.8),针对有症状新冠病毒病为97.0%(96.7 - 97.2;每100000人日32.5对0.8),针对与新冠病毒病相关的住院为97.2%(96.8 - 97.5;每100000人日4.6对0.3),针对重症或危重症与新冠病毒病相关的住院为97.5%(97.1 - 97.8;每100000人日2.7对0.2),针对与新冠病毒病相关的死亡为96.7%(96.0 - 97.3;每100000人日0.6对0.1)。在所有年龄组中,随着疫苗接种覆盖率的增加,SARS-CoV-2感染结果的发病率下降。在8472份检测样本中,8006份显示刺突基因靶点失败,估计在SARS-CoV-2感染中B.1.1.7变异株的流行率为94.5%。

解读

两剂BNT162b2在所有年龄组(≥16岁,包括≥85岁的老年人)中对预防有症状和无症状SARS-CoV-2感染以及与新冠病毒病相关的住院、重症疾病和死亡(包括由B.1.1.7 SARS-CoV-2变异株引起的)非常有效。随着疫苗接种覆盖率的增加,SARS-CoV-2发病率显著且持续下降。这些发现表明新冠病毒病疫苗接种有助于控制疫情。

资金来源

无。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fba4/8099315/f8721066ee8b/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fba4/8099315/ba976c8062d1/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fba4/8099315/f8721066ee8b/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fba4/8099315/ba976c8062d1/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fba4/8099315/f8721066ee8b/gr2_lrg.jpg

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