The University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
The University of Pennsylvania Health System, Philadelphia, Pennsylvania, USA.
Clin Infect Dis. 2023 Feb 8;76(3):e319-e326. doi: 10.1093/cid/ciac454.
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant has spread rapidly throughout the world since being identified in South Africa in November 2021. Few studies have assessed primary series and booster vaccine effectiveness against Omicron among US healthcare workers.
We conducted a test-negative case-control design to estimate BNT162b2 and mRNA1273 primary vaccination and booster effectiveness against SARS-CoV-2 infection and symptomatic coronavirus disease 2019 during an Omicron surge among employees of the University of Pennsylvania Health System. The study period was between 1 July 2021 and 5 April 2022. We defined the Delta period as 1 July to 12 December 2021 and the Omicron period as beginning 12 December 21.
Our sample included 14 520 tests (2776 [19%] positive)-7422 (506 [7%] positive) during Delta and 7098 (2270 [32%] positive) during Omicron. Benchmarked against Delta, the vaccine effectiveness of 2 vaccine doses was lower during Omicron, with no significant protection against infection. Booster doses added significant protection, although they also showed reduced effectiveness during Omicron. Compared with findings in employees who had received 2 vaccine doses, 3 doses of BNT162b2 had a relative effectiveness of 50% (95% confidence interval, 42%-56%) during Omicron, relative to 78% (63%-87%) during Delta; 3 doses of mRNA1273 had a relative effectiveness of 56% (45%-65%) during Omicron, relative to 96% (82%-99%) during Delta. Restricting the sample to symptomatic tests yielded similar results to our primary analysis. After initial waning in BNT162b2 booster protection against infection, it remained largely stable for ≥16 weeks after vaccination.
Our findings provide a strong rationale for boosters among healthcare workers in the Omicron era.
自 2021 年 11 月在南非发现严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)奥密克戎变异株以来,该变异株已迅速在全球传播。很少有研究评估过美国医护人员接种初级系列和加强针疫苗对奥密克戎的有效性。
我们采用了一项病例对照研究,以评估宾夕法尼亚大学卫生系统员工在奥密克戎疫情期间,BNT162b2 和 mRNA1273 初级疫苗接种和加强针预防 SARS-CoV-2 感染和有症状的 2019 年冠状病毒病的效果。研究期间为 2021 年 7 月 1 日至 2022 年 4 月 5 日。我们将德尔塔时期定义为 2021 年 7 月 1 日至 12 月 12 日,奥密克戎时期为 2021 年 12 月 12 日开始。
我们的样本包括 14520 次检测(2776 次[19%]阳性)-7422 次(506 次[7%]阳性)在德尔塔时期和 7098 次(2270 次[32%]阳性)在奥密克戎时期。与德尔塔时期相比,奥密克戎时期,两剂疫苗的疫苗有效性较低,对感染没有显著保护作用。加强针增加了显著的保护作用,但在奥密克戎时期也显示出效力降低。与接受两剂疫苗的员工的发现相比,在奥密克戎时期,BNT162b2 的三剂疫苗的相对有效性为 50%(95%置信区间,42%-56%),而在德尔塔时期为 78%(63%-87%);在奥密克戎时期,mRNA1273 的三剂疫苗的相对有效性为 56%(45%-65%),而在德尔塔时期为 96%(82%-99%)。将样本限制在有症状的检测中,得出的结果与我们的主要分析相似。在 BNT162b2 加强针对感染的保护作用最初减弱后,在接种疫苗后至少 16 周内基本保持稳定。
我们的研究结果为奥密克戎时代医护人员接种加强针提供了有力依据。