Department of Infectious Disease Epidemiology, Robert Koch Institute, Berlin, Germany.
Centre for International Health Protection, Robert Koch Institute, Berlin, Germany.
Front Immunol. 2022 Aug 24;13:940562. doi: 10.3389/fimmu.2022.940562. eCollection 2022.
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant is currently the dominant variant globally. This third interim analysis of a living systematic review summarizes evidence on the effectiveness of the coronavirus disease 2019 (COVID-19) vaccine (vaccine effectiveness, VE) and duration of protection against Omicron.
We systematically searched literature on COVID-19 for controlled studies, evaluating the effectiveness of COVID-19 vaccines approved in the European Union up to 14/01/2022, complemented by hand searches of websites and metasearch engines up to 11/02/2022. We considered the following comparisons: full primary immunization vs. no vaccination, booster immunization vs. no vaccination, and booster vs. full primary immunization. VE against any confirmed SARS-CoV-2 infection, symptomatic, and severe COVID-19 (i.e., COVID-19-related hospitalization, ICU admission, or death) was indicated, providing estimate ranges. Meta-analysis was not performed due to high study heterogeneity. The risk of bias was assessed with ROBINS-I, and the certainty of the evidence was evaluated using GRADE.
We identified 26 studies, including 430 to 2.2 million participants, which evaluated VE estimates against infections with the SARS-CoV-2 Omicron variant. VE against any confirmed SARS-CoV-2 infection ranged between 0-62% after full primary immunization and between 34-66% after a booster dose compared to no vaccination. VE range for booster vs. full primary immunization was 34-54.6%. After full primary immunization VE against symptomatic COVID-19 ranged between 6-76%. After booster immunization VE ranged between 3-84% compared to no vaccination and between 56-69% compared to full primary immunization. VE against severe COVID-19 ranged between 3-84% after full primary immunization and between 12-100% after booster immunization compared to no vaccination, and 100% (95% CI 71.4-100) compared to full primary immunization (data from only one study). VE was characterized by a moderate to strong decline within 3-6 months for SARS-CoV-2 infections and symptomatic COVID-19. Against severe COVID-19, protection remained robust for at least up to 6 months. Waning immunity was more profound after primary than booster immunization. The risk of bias was moderate to critical across studies and outcomes. GRADE certainty was very low for all outcomes.
Under the Omicron variant, the effectiveness of EU-licensed COVID-19 vaccines in preventing any SARS-CoV-2 infection is low and only short-lasting after full primary immunization, but can be improved by booster vaccination. VE against severe COVID-19 remains high and is long-lasting, especially after receiving the booster vaccination.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的奥密克戎变体目前是全球的主要变体。本研究对一项正在进行的系统评价的第三次中期分析总结了 COVID-19 疫苗(疫苗有效性,VE)对奥密克戎的有效性和保护持续时间的证据。
我们系统地检索了 COVID-19 的文献,评估了截至 2022 年 1 月 14 日在欧盟批准的 COVID-19 疫苗的有效性,补充了截至 2022 年 2 月 11 日对手册搜索网站和元搜索引擎的搜索。我们考虑了以下比较:全初级免疫与无接种、加强免疫与无接种以及加强免疫与全初级免疫。表明对任何确认的 SARS-CoV-2 感染、症状性和严重 COVID-19(即 COVID-19 相关住院、入住 ICU 或死亡)的 VE,提供估计范围。由于研究异质性高,未进行荟萃分析。使用 ROBINS-I 评估偏倚风险,并使用 GRADE 评估证据确定性。
我们确定了 26 项研究,其中包括 430 至 220 万人参与,评估了针对 SARS-CoV-2 奥密克戎变体感染的 VE 估计值。与无接种相比,全初级免疫后的任何确认的 SARS-CoV-2 感染的 VE 范围在 0-62%之间,而加强免疫后的 VE 范围在 34-66%之间。与全初级免疫相比,加强免疫与全初级免疫的 VE 范围为 34-54.6%。全初级免疫后,针对症状性 COVID-19 的 VE 范围在 6-76%之间。与无接种相比,加强免疫后的 VE 范围在 3-84%之间,与全初级免疫相比,VE 范围在 56-69%之间。与无接种相比,全初级免疫后针对严重 COVID-19 的 VE 范围在 3-84%之间,加强免疫后在 12-100%之间,与全初级免疫相比为 100%(95%CI71.4-100)(来自一项研究的数据)。VE 的特点是在 3-6 个月内针对 SARS-CoV-2 感染和症状性 COVID-19 的下降幅度较大。针对严重 COVID-19,至少在 6 个月内保持强大的保护作用。初级免疫后的免疫下降比加强免疫更为明显。在所有研究和结果中,偏倚风险均为中度至高度。所有结果的 GRADE 确定性均为极低。
在奥密克戎变体下,欧盟许可的 COVID-19 疫苗在预防任何 SARS-CoV-2 感染方面的有效性较低,并且在全初级免疫后仅持续短暂时间,但可通过加强接种来提高。针对严重 COVID-19 的 VE 仍然很高且持久,尤其是在接受加强接种后。