Kahn Sagol Maccabi Research and Innovation Center, Maccabi Healthcare Services, Tel Aviv, Israel.
Maccabitech Institute for Research and Innovation, Maccabi Healthcare Services, Tel Aviv, Israel.
JAMA Intern Med. 2022 Feb 1;182(2):179-184. doi: 10.1001/jamainternmed.2021.7382.
With the evidence of waning immunity of the mRNA vaccine BNT162b2 (Pfizer-BioNTech), a nationwide third-dose (booster) vaccination campaign was initiated in Israel during August 2021; other countries have begun to administer a booster shot as well.
To evaluate the initial short-term additional benefit of a 3-dose vs a 2-dose regimen against infection of SARS-CoV-2.
DESIGN, SETTING, AND PARTICIPANTS: This preliminary retrospective case-control study used 2 complementary approaches: a test-negative design and a matched case-control design. Participants were included from the national centralized database of Maccabi Healthcare Services, an Israeli healthcare maintenance organization covering 2.5 million members. Data were collected between March 1, 2020, and October 4, 2021, and analyses focused on the period from August 1, 2021, to October 4, 2021, because the booster dose was widely administered from August 1 onward.
Either 2 doses or 3 doses of the BNT162b2 vaccine.
The reduction in the odds of a positive SARS-CoV-2 polymerase chain reaction (PCR) test at different time intervals following receipt of the booster dose (0-6, 7-13, 14-20, 21-27, and 28-65 days) compared with receiving only 2 doses.
The study population included 306 710 members of Maccabi Healthcare Services who were 40 years and older (55% female) and received either 2 or 3 doses of the BNT162b2 vaccine and did not have a positive PCR test result for SARS-CoV-2 prior to the start of the follow-up period. During this period, there were 500 232 PCR tests performed, 227 380 among those who received 2 doses and 272 852 among those who received 3 doses, with 14 989 (6.6%) and 4941 (1.8%) positive test results in each group, respectively. Comparing those who received a booster and those who received 2 doses, there was an estimated odds ratio of 0.14 (95% CI, 0.13-0.15) 28 to 65 days following receipt of the booster (86% reduction in the odds of testing positive for SARS-CoV-2).
Previous studies have demonstrated that vaccine-derived protection against SARS-CoV-2 wanes over time. In this case-control analysis, we showed an association between receipt of the booster dose and a reduction in the odds of testing positive for SARS-CoV-2, potentially counteracting waning immunity in the short term. Further monitoring of data from this population is needed to determine the duration of immunity following the booster.
随着 mRNA 疫苗 BNT162b2(辉瑞-生物科技)免疫效力的减弱,以色列于 2021 年 8 月启动了全国范围内的第三剂(加强针)接种运动;其他国家也开始接种加强针。
评估 3 剂与 2 剂方案对感染 SARS-CoV-2 的短期额外益处。
设计、地点和参与者:本初步回顾性病例对照研究使用了 2 种互补方法:阴性检测设计和匹配病例对照设计。参与者来自以色列医疗保健服务的国家集中数据库 Maccabi Healthcare Services,该组织覆盖了 250 万成员。数据收集于 2020 年 3 月 1 日至 2021 年 10 月 4 日,分析重点集中在 2021 年 8 月 1 日至 2021 年 10 月 4 日期间,因为从 8 月 1 日起广泛接种了加强针。
2 剂或 3 剂 BNT162b2 疫苗。
与仅接受 2 剂相比,在接受加强针后不同时间间隔(0-6、7-13、14-20、21-27 和 28-65 天)检测到 SARS-CoV-2 聚合酶链反应(PCR)检测呈阳性的可能性降低。
研究人群包括 Maccabi Healthcare Services 的 306710 名 40 岁及以上(55%为女性)的成员,他们接受了 2 剂或 3 剂 BNT162b2 疫苗,并且在随访开始前没有 SARS-CoV-2 的 PCR 检测阳性结果。在此期间,进行了 500232 次 PCR 检测,其中 227380 次接受 2 剂,272852 次接受 3 剂,每组分别有 14989(6.6%)和 4941(1.8%)阳性检测结果。与接受加强针的人群相比,接受加强针的人群估计比值比为 0.14(95%CI,0.13-0.15),28 至 65 天内 SARS-CoV-2 检测呈阳性的几率降低了 86%。
之前的研究表明,疫苗对 SARS-CoV-2 的保护效力会随时间减弱。在这项病例对照分析中,我们发现加强针接种与 SARS-CoV-2 检测呈阳性几率降低之间存在关联,这可能在短期内对抗免疫效力的减弱。需要进一步监测该人群的数据,以确定加强针接种后的免疫持续时间。