McKeigue Paul M, McAllister David A, Hutchinson Sharon J, Robertson Chris, Stockton Diane, Colhoun Helen M
Usher Institute, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, UK; Public Health Scotland, Glasgow, UK.
Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK; Public Health Scotland, Glasgow, UK.
Lancet Respir Med. 2022 Jun;10(6):566-572. doi: 10.1016/S2213-2600(22)00045-5. Epub 2022 Feb 25.
Reports have suggested that the efficacy of vaccines against COVID-19 might have fallen since the delta (B.1.617.2) SARS-CoV-2 variant replaced the alpha (B.1.1.7) variant as the predominant variant. We aimed to investigate, for the two main classes of vaccine, whether efficacy against severe COVID-19 has decreased since delta became the predominant variant and whether the efficacy of two doses of vaccine against severe COVID-19 wanes with time since second dose.
In the REACT-SCOT case-control study, vaccine efficacy was estimated using a matched case-control design that includes all diagnosed cases of COVID-19 in Scotland up to Sept 8, 2021. For every incident case of COVID-19 in the Scottish population, ten controls matched for age rounded to the nearest year, sex, and primary care practice, and alive on the day of presentation of the case that they were matched to were selected using the Community Health Index database. To minimise ascertainment bias we prespecified the primary outcome measure to assess vaccine efficacy as severe COVID-19, defined as diagnosed patients with entry to critical care within 21 days of first positive test, death within 28 days of first positive test, or any death for which COVID-19 was coded as underlying cause. Although the data extracted for this study included cases presenting up to Sept 22, 2021, the analyses reported here are restricted to cases and controls presenting from Dec 1, 2020, to Sept 8, 2021, ensuring follow-up for at least 14 days after presentation date to allow classification of hospitalisation and (for most cases) severity based on entry to critical care or fatal outcome.
During the study period, a total of 5645 severe cases of COVID-19 were recorded; these were matched to 50 096 controls. Of the severe cases, 4495 (80%) were not vaccinated, and of the controls, 36 879 (74%) were not vaccinated. Of the severe cases of COVID-19 who had been vaccinated, 389 had received an mRNA vaccine and 759 had received the ChAdOx1 vaccine. The efficacy of vaccination against severe COVID-19 decreased in May, 2021, coinciding with the replacement of the alpha SARS-CoV-2 variant by the delta variant in Scotland, but this decrease was reversed over the following month. In the most recent time window centred on July 29, 2021, the efficacy of two doses was 91% (95% CI 87-94) for the ChAdOx1 vaccine and 92% (88-95) for mRNA (Pfizer or Moderna) vaccines. The efficacy of the ChAdOx1 vaccine against severe COVID-19 declined with time since second dose to 69% (95% CI 52-80) at 20 weeks from second dose. The efficacy of mRNA vaccines declined in the first ten weeks from second dose but more slowly thereafter to 93% (88-96) at 20 weeks from second dose.
Our results are reassuring with respect to concerns that vaccine efficacy against severe COVID-19 might have fallen since the delta variant became predominant, or that efficacy of mRNA vaccines wanes within the first 5-6 months after second dose. However, the efficacy of the ChAdOx1 vaccine against severe COVID-19 wanes substantially by 20 weeks from second dose. Efficacy of mRNA vaccines after 20 weeks and against newer variants remains to be established. Our findings support the case for additional protective measures for those at risk of severe disease, including, but not limited to, booster doses, at times when transmission rates are high or expected to rise.
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有报告表明,自新冠病毒德尔塔(B.1.617.2)变体取代阿尔法(B.1.1.7)变体成为主要变体以来,针对新冠病毒的疫苗效力可能有所下降。我们旨在调查,对于两类主要疫苗,自德尔塔变体成为主要变体以来,针对重症新冠病毒疾病的效力是否降低,以及两剂疫苗针对重症新冠病毒疾病的效力是否会随着自第二剂接种后的时间推移而减弱。
在REACT - SCOT病例对照研究中,采用匹配病例对照设计估计疫苗效力,该设计纳入了截至2021年9月8日在苏格兰所有确诊的新冠病毒疾病病例。对于苏格兰人群中每一例新冠病毒疾病的新发病例,使用社区健康指数数据库选取十名对照,对照按年龄(四舍五入到最接近的年份)、性别和基层医疗服务机构进行匹配,且在与其匹配的病例就诊当天仍存活。为尽量减少确诊偏倚,我们预先指定主要结局指标为评估针对重症新冠病毒疾病的疫苗效力,重症新冠病毒疾病定义为首次核酸检测呈阳性后21天内进入重症监护病房的确诊患者、首次核酸检测呈阳性后28天内死亡的患者,或任何将新冠病毒疾病列为根本死因的死亡病例。尽管本研究提取的数据包括截至2021年9月22日就诊的病例,但此处报告的分析仅限于2020年12月1日至2021年9月8日就诊的病例和对照,以确保在就诊日期后至少随访14天,以便根据进入重症监护病房情况或致命结局对住院情况(以及大多数病例的病情严重程度)进行分类。
在研究期间,共记录了5645例重症新冠病毒疾病病例;这些病例与50096名对照进行了匹配。在重症病例中,4495例(80%)未接种疫苗,在对照中,36879例(74%)未接种疫苗。在接种过疫苗的重症新冠病毒疾病病例中,389例接种了信使核糖核酸疫苗,759例接种了ChAdOx1疫苗。针对重症新冠病毒疾病的疫苗效力在2021年5月有所下降,这与苏格兰的阿尔法新冠病毒变体被德尔塔变体取代的时间一致,但在接下来的一个月中这种下降趋势得到扭转。在以2021年7月29日为中心的最近一个时间窗口中,ChAdOx1疫苗两剂的效力为91%(95%置信区间87 - 94),信使核糖核酸(辉瑞或莫德纳)疫苗两剂的效力为92%(88 - 95)。ChAdOx1疫苗针对重症新冠病毒疾病的效力随着自第二剂接种后的时间推移而下降,在第二剂接种后20周时降至69%(95%置信区间52 - 80)。信使核糖核酸疫苗的效力在第二剂接种后的前十周下降,但此后下降速度较慢,在第二剂接种后20周时降至93%(88 - 96)。
我们的结果对于以下担忧是令人安心的,即自德尔塔变体成为主要变体以来,针对重症新冠病毒疾病的疫苗效力可能下降,或者信使核糖核酸疫苗的效力在第二剂接种后的前5 - 6个月内会减弱。然而,ChAdOx1疫苗针对重症新冠病毒疾病的效力在第二剂接种后20周时大幅下降。信使核糖核酸疫苗在20周后的效力以及针对更新变体的效力仍有待确定。我们的研究结果支持在传播率高或预计会上升时,为重症疾病风险人群采取额外保护措施的建议,包括但不限于加强针接种。
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