MMWR Morb Mortal Wkly Rep. 2022 Jan 21;71(4):139-145. doi: 10.15585/mmwr.mm7104e3.
Estimates of COVID-19 mRNA vaccine effectiveness (VE) have declined in recent months (1,2) because of waning vaccine induced immunity over time,* possible increased immune evasion by SARS-CoV-2 variants (3), or a combination of these and other factors. CDC recommends that all persons aged ≥12 years receive a third dose (booster) of an mRNA vaccine ≥5 months after receipt of the second mRNA vaccine dose and that immunocompromised individuals receive a third primary dose. A third dose of BNT162b2 (Pfizer-BioNTech) COVID-19 vaccine increases neutralizing antibody levels (4), and three recent studies from Israel have shown improved effectiveness of a third dose in preventing COVID-19 associated with infections with the SARS-CoV-2 B.1.617.2 (Delta) variant (5-7). Yet, data are limited on the real-world effectiveness of third doses of COVID-19 mRNA vaccine in the United States, especially since the SARS-CoV-2 B.1.1.529 (Omicron) variant became predominant in mid-December 2021. The VISION Network examined VE by analyzing 222,772 encounters from 383 emergency departments (EDs) and urgent care (UC) clinics and 87,904 hospitalizations from 259 hospitals among adults aged ≥18 years across 10 states from August 26, 2021 to January 5, 2022. Analyses were stratified by the period before and after the Omicron variant became the predominant strain (>50% of sequenced viruses) at each study site. During the period of Delta predominance across study sites in the United States (August-mid-December 2021), VE against laboratory-confirmed COVID-19-associated ED and UC encounters was 86% 14-179 days after dose 2, 76% ≥180 days after dose 2, and 94% ≥14 days after dose 3. Estimates of VE for the same intervals after vaccination during Omicron variant predominance were 52%, 38%, and 82%, respectively. During the period of Delta variant predominance, VE against laboratory-confirmed COVID-19-associated hospitalizations was 90% 14-179 days after dose 2, 81% ≥180 days after dose 2, and 94% ≥14 days after dose 3. During Omicron variant predominance, VE estimates for the same intervals after vaccination were 81%, 57%, and 90%, respectively. The highest estimates of VE against COVID-19-associated ED and UC encounters or hospitalizations during both Delta- and Omicron-predominant periods were among adults who received a third dose of mRNA vaccine. All unvaccinated persons should get vaccinated as soon as possible. All adults who have received mRNA vaccines during their primary COVID-19 vaccination series should receive a third dose when eligible, and eligible persons should stay up to date with COVID-19 vaccinations.
关于 COVID-19 mRNA 疫苗有效性(VE)的估计值在最近几个月有所下降(1,2),这是由于疫苗诱导的免疫随时间逐渐减弱*、SARS-CoV-2 变体(3)的免疫逃逸能力可能增加,或者是这些因素和其他因素的综合作用。CDC 建议所有年龄≥12 岁的人在接受第二剂 mRNA 疫苗后≥5 个月接受第三剂(加强针)mRNA 疫苗,免疫功能低下者接受第三剂基础剂量。接受第三剂 BNT162b2(辉瑞-生物科技)COVID-19 疫苗可以提高中和抗体水平(4),最近来自以色列的三项研究表明,在预防与 SARS-CoV-2 B.1.617.2(Delta)变体(5-7)相关的 COVID-19 感染方面,第三剂的有效性有所提高。然而,在美国,关于 COVID-19 mRNA 疫苗第三剂的真实世界有效性的数据有限,尤其是自 2021 年 12 月中旬 SARS-CoV-2 B.1.1.529(Omicron)变体成为主要流行株以来。VISION 网络通过分析 2021 年 8 月 26 日至 2022 年 1 月 5 日期间美国 10 个州的 383 个急诊部门(ED)和紧急护理(UC)诊所的 222,772 次就诊以及 259 家医院的 87,904 例住院情况,评估了 VE。分析按每个研究点在 Omicron 变体成为主要菌株(>50%的测序病毒)之前和之后的时期进行分层。在美国各研究点 Delta 占主导地位期间(2021 年 8 月至 12 月中旬),接种第二剂后 14-179 天、≥180 天和≥14 天,接种第二剂后 14-179 天,接种第三剂后 76%和 94%对实验室确诊的 COVID-19 相关 ED 和 UC 就诊有保护作用。在 Omicron 变体占主导地位期间,接种疫苗后相同时间间隔的 VE 估计值分别为 52%、38%和 82%。在 Delta 变体占主导地位期间,接种第二剂后 14-179 天、≥180 天和≥14 天,接种第二剂后 90%、81%和 94%对实验室确诊的 COVID-19 相关住院有保护作用。在 Omicron 变体占主导地位期间,接种疫苗后相同时间间隔的 VE 估计值分别为 81%、57%和 90%。在 Delta 和 Omicron 占主导地位期间,对 COVID-19 相关 ED 和 UC 就诊或住院的最高 VE 估计值均出现在接种第三剂 mRNA 疫苗的成年人中。所有未接种疫苗的人都应尽快接种疫苗。所有在其初级 COVID-19 疫苗接种系列中接受过 mRNA 疫苗的成年人在符合条件时应接种第三剂,符合条件者应及时接种 COVID-19 疫苗。