Paz-Bailey Gabriela, Sternberg Maya, Kugeler Kiersten, Hoots Brooke, Amin Avnika B, Johnson Amelia G, Barbeau Bree, Bayoumi Nagla S, Bertolino Daniel, Boulton Rachelle, Brown Catherine M, Busen Katherine, Cima Michael, Drenzek Cherie, Gent Ashley, Haney Gillian, Hicks Liam, Hook Sarah, Jara Amanda, Jones Amanda, Kamal-Ahmed Ishrat, Kangas Sarah, Kanishka F N U, Khan Saadiah I, Kirkendall Samantha K, Kocharian Anna, Lyons B Casey, Lauro Priscilla, McCormick Donald, McMullen Chelsea, Milroy Lauren, Reese Heather E, Sell Jessica, Sierocki Allison, Smith Elizabeth, Sosin Daniel, Stanislawski Emma, Strand Kyle, Troelstrup Thomas, Turner Kathryn A, Vest Hailey, Warner Sydni, Wiedeman Caleb, Silk Benjamin, Scobie Heather M
Epidemiology Task Force, COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta.
Utah Department of Health, Salt Lake City.
NEJM Evid. 2022 Jan 10;1(3). doi: 10.1056/evidoa2100057.
With the emergence of the delta variant, the United States experienced a rapid increase in Covid-19 cases in 2021. We estimated the risk of breakthrough infection and death by month of vaccination as a proxy for waning immunity during a period of delta variant predominance.
Covid-19 case and death data from 15 U.S. jurisdictions during January 3 to September 4, 2021 were used to estimate weekly hazard rates among fully vaccinated persons, stratified by age group and vaccine product. Case and death rates during August 1 to September 4, 2021 were presented across four cohorts defined by month of vaccination. Poisson models were used to estimate adjusted rate ratios comparing the earlier cohorts to July rates.
During August 1 to September 4, 2021, case rates per 100,000 person-weeks among all vaccine recipients for the January to February, March to April, May to June, and July cohorts were 168.8 (95% confidence interval [CI], 167.5 to 170.1), 123.5 (95% CI, 122.8 to 124.1), 83.6 (95% CI, 82.9 to 84.3), and 63.1 (95% CI, 61.6 to 64.6), respectively. Similar trends were observed by age group for BNT162b2 (Pfizer-BioNTech) and mRNA-1273 (Moderna) vaccine recipients. Rates for the Ad26.COV2.S (Janssen-Johnson & Johnson) vaccine were higher; however, trends were inconsistent. BNT162b2 vaccine recipients 65 years of age or older had higher death rates among those vaccinated earlier in the year. Protection against death was sustained for the mRNA-1273 vaccine recipients. Across age groups and vaccine types, people who were vaccinated 6 months ago or longer (January-February) were 3.44 (3.36 to 3.53) times more likely to be infected and 1.70 (1.29 to 2.23) times more likely to die from COVID-19 than people vaccinated recently in July 2021.
Our study suggests that protection from SARS-CoV-2 infection among all ages or death among older adults waned with increasing time since vaccination during a period of delta predominance. These results add to the evidence base that supports U.S. booster recommendations, especially for older adults vaccinated with BNT162b2 and recipients of the Ad26.COV2.S vaccine. (Funded by the Centers for Disease Control and Prevention.).
随着德尔塔变异株的出现,美国在2021年新冠病毒病(Covid-19)病例迅速增加。我们估算了按接种月份划分的突破性感染和死亡风险,以此作为在德尔塔变异株占主导期间免疫力下降的一个指标。
利用2021年1月3日至9月4日期间美国15个司法管辖区的Covid-19病例和死亡数据,估算完全接种疫苗者的每周风险率,并按年龄组和疫苗产品进行分层。2021年8月1日至9月4日期间的病例和死亡率按接种月份定义的四个队列呈现。采用泊松模型估算调整后的率比,将早期队列与7月的率进行比较。
在2021年8月1日至9月4日期间,1月至2月、3月至4月、5月至6月以及7月队列中,每10万人周的所有疫苗接种者的病例率分别为168.8(95%置信区间[CI],167.5至170.1)、123.5(95%CI,122.8至124.1)、83.6(95%CI,82.9至84.3)和63.1(95%CI,61.6至64.6)。对于接种BNT162b2(辉瑞 - 生物科技公司)和mRNA - 1273(莫德纳公司)疫苗的受种者,各年龄组均观察到类似趋势。Ad26.COV2.S(杨森 - 强生公司)疫苗的比率较高;然而,趋势并不一致。65岁及以上接种BNT162b2疫苗的受种者在当年较早接种疫苗的人群中死亡率较高。mRNA - 1273疫苗受种者对死亡的保护作用持续存在。在各年龄组和疫苗类型中,6个月前或更早(1月至2月)接种疫苗的人感染新冠病毒的可能性是2021年7月最近接种疫苗者的3.44(3.36至3.53)倍,死于新冠病毒病的可能性是其1.70(1.29至2.23)倍。
我们的研究表明,在德尔塔变异株占主导期间,各年龄段对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的防护或老年人的死亡防护会随着接种后时间的增加而减弱。这些结果为支持美国加强针建议,尤其是针对接种BNT162b2疫苗的老年人和Ad26.COV2.S疫苗受种者的建议,增添了证据基础。(由美国疾病控制与预防中心资助。)