Department of Oncology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
JAMA. 2022 Jan 25;327(4):341-349. doi: 10.1001/jama.2021.23641.
Administration of a BNT162b2 booster dose (Pfizer-BioNTech) to fully vaccinated individuals aged 60 years and older was significantly associated with lower risk of SARS-CoV-2 infection and severe illness. Data are lacking on the effectiveness of booster doses for younger individuals and health care workers.
To estimate the association of a BNT162b2 booster dose with SARS-CoV-2 infections among health care workers who were previously vaccinated with a 2-dose series of BNT162b2.
DESIGN, SETTING, AND PARTICIPANTS: This was a prospective cohort study conducted at a tertiary medical center in Tel Aviv, Israel. The study cohort included 1928 immunocompetent health care workers who were previously vaccinated with a 2-dose series of BNT162b2, and had enrolled between August 8 and 19, 2021, with final follow-up reported through September 20, 2021. Screening for SARS-CoV-2 infection was performed every 14 days. Anti-spike protein receptor binding domain IgG titers were determined at baseline and 1 month after enrollment. Cox regression with time-dependent analysis was used to estimate hazard ratios of SARS-CoV-2 infection between booster-immunized status and 2-dose vaccinated (booster-nonimmunized) status.
Vaccination with a booster dose of BNT162b2 vaccine.
The primary outcome was SARS-CoV-2 infection, as confirmed by reverse transcriptase-polymerase chain reaction.
Among 1928 participants, the median age was 44 years (IQR, 36-52 years) and 1381 were women (71.6%). Participants completed the 2-dose vaccination series a median of 210 days (IQR, 205-213 days) before study enrollment. A total of 1650 participants (85.6%) received the booster dose. During a median follow-up of 39 days (IQR, 35-41 days), SARS-CoV-2 infection occurred in 44 participants (incidence rate, 60.2 per 100 000 person-days); 31 (70.5%) were symptomatic. Five SARS-CoV-2 infections occurred in booster-immunized participants and 39 in booster-nonimmunized participants (incidence rate, 12.8 vs 116 per 100 000 person-days, respectively). In a time-dependent Cox regression analysis, the adjusted hazard ratio of SARS-CoV-2 infection for booster-immunized vs booster-nonimmunized participants was 0.07 (95% CI, 0.02-0.20).
Among health care workers at a single center in Israel who were previously vaccinated with a 2-dose series of BNT162b2, administration of a booster dose compared with not receiving one was associated with a significantly lower rate of SARS-CoV-2 infection over a median of 39 days of follow-up. Ongoing surveillance is required to assess durability of the findings.
为 60 岁及以上的完全接种疫苗者接种 BNT162b2 加强针与降低 SARS-CoV-2 感染和重症疾病的风险显著相关。关于较年轻个体和医护人员接种加强针的有效性的数据尚缺乏。
估计对先前接受过 2 剂 BNT162b2 疫苗接种的医护人员接种 BNT162b2 加强针与 SARS-CoV-2 感染之间的关联。
设计、地点和参与者:这是在以色列特拉维夫的一家三级医疗中心进行的前瞻性队列研究。研究队列包括 1928 名免疫功能正常的医护人员,他们之前已接受过 2 剂 BNT162b2 疫苗接种,并于 2021 年 8 月 8 日至 19 日之间入组,最终随访报告截至 2021 年 9 月 20 日。每 14 天进行一次 SARS-CoV-2 感染筛查。在基线和入组后 1 个月测定抗刺突蛋白受体结合域 IgG 滴度。采用时依 Cox 回归分析估计 SARS-CoV-2 感染在加强免疫状态和 2 剂接种(加强免疫非接种)状态之间的风险比。
接受 BNT162b2 疫苗加强针接种。
主要结局是通过逆转录酶-聚合酶链反应(RT-PCR)确认的 SARS-CoV-2 感染。
在 1928 名参与者中,中位年龄为 44 岁(IQR,36-52 岁),1381 名女性(71.6%)。参与者在研究入组前中位完成 2 剂疫苗接种系列 210 天(IQR,205-213 天)。共有 1650 名参与者(85.6%)接受了加强针接种。在中位随访 39 天(IQR,35-41 天)期间,44 名参与者发生了 SARS-CoV-2 感染(发病率为 60.2/100000 人-日);31 名(70.5%)为有症状感染者。5 例 SARS-CoV-2 感染发生在加强免疫接种者中,39 例发生在加强免疫非接种者中(发病率分别为 12.8/100000 人-日和 116/100000 人-日)。在时间依赖性 Cox 回归分析中,与加强免疫非接种者相比,加强免疫接种者 SARS-CoV-2 感染的调整后风险比为 0.07(95%CI,0.02-0.20)。
在以色列一家单中心的医护人员中,与未接种加强针相比,接种加强针与中位 39 天随访期间 SARS-CoV-2 感染率显著降低相关。需要持续监测以评估结果的持久性。