Andrejko Kristin L, Pry Jake M, Myers Jennifer F, Mehrotra Megha, Lamba Katherine, Lim Esther, Fukui Nozomi, DeGuzman Jennifer L, Openshaw John, Watt James, Jain Seema, Lewnard Joseph A, Covid-Case-Control Study Team On Behalf Of The California
Am J Epidemiol. 2023 Jun 2;192(6):895-907. doi: 10.1093/aje/kwad017.
Concerns about the duration of protection conferred by coronavirus disease 2019 (COVID-19) vaccines have arisen in postlicensure evaluations. "Depletion of susceptibles," a bias driven by differential accrual of infection among vaccinated and unvaccinated individuals, may obscure vaccine effectiveness (VE) estimates, hindering interpretation. We enrolled California residents who received molecular SARS-CoV-2 tests in a matched, test-negative design, case-control study to estimate VE of mRNA-based COVID-19 vaccines between February 23 and December 5, 2021. We analyzed waning protection following 2 vaccine doses using conditional logistic regression models. Additionally, we used data from a population-based serological study to adjust for "depletion-of-susceptibles" bias and estimated VE for 3 doses, by time since second dose receipt. Pooled VE of BNT162b2 and mRNA-1273 against symptomatic SARS-CoV-2 infection was 91.3% (95% confidence interval (CI): 83.8, 95.4) at 14 days after second-dose receipt and declined to 50.8% (95% CI: 19.7, 69.8) at 7 months. Adjusting for depletion-of-susceptibles bias, we estimated VE of 53.2% (95% CI: 23.6, 71.2) at 7 months after primary mRNA vaccination series. A booster dose of BN162b2 or mRNA-1273 increased VE to 95.0% (95% CI: 82.8, 98.6). These findings confirm that observed waning of protection is not attributable to epidemiologic bias and support ongoing efforts to administer additional vaccine doses to mitigate burden of COVID-19.
在新冠病毒2019(COVID-19)疫苗获得许可后的评估中,人们对其提供的保护持续时间产生了担忧。“易感人群的减少”是一种由接种疫苗和未接种疫苗个体之间感染累积差异导致的偏差,可能会掩盖疫苗效力(VE)的估计值,从而妨碍解读。我们在一项匹配的、检测呈阴性设计的病例对照研究中,纳入了接受过新冠病毒分子检测的加利福尼亚居民,以估计2021年2月23日至12月5日期间基于mRNA的COVID-19疫苗的VE。我们使用条件逻辑回归模型分析了两剂疫苗后保护作用的减弱情况。此外,我们利用一项基于人群的血清学研究数据,对“易感人群减少”偏差进行调整,并按自接种第二剂疫苗后的时间,估计了三剂疫苗的VE。BNT162b2和mRNA-1273针对有症状的SARS-CoV-2感染的合并VE在接种第二剂疫苗后14天为91.3%(95%置信区间(CI):83.8,95.4),在7个月时降至50.8%(95%CI:19.7,69.8)。调整“易感人群减少”偏差后,我们估计在完成mRNA初次疫苗接种系列7个月后,VE为53.2%(95%CI:23.6,71.2)。一剂BN162b2或mRNA-1273加强针可将VE提高至95.0%(95%CI:82.8,98.6)。这些发现证实,观察到的保护作用减弱并非归因于流行病学偏差,并支持持续努力接种额外剂量疫苗以减轻COVID-19负担。