Department of Immunizations, Vaccines and Biologicals, World Health Organization, Geneva, Switzerland.
International Vaccine Access Center, Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Vaccine. 2023 Mar 31;41(14):2329-2338. doi: 10.1016/j.vaccine.2023.02.020. Epub 2023 Feb 9.
Emerging in November 2021, the SARS-CoV-2 Omicron variant of concern exhibited marked immune evasion resulting in reduced vaccine effectiveness against SARS-CoV-2 infection and symptomatic disease. Most vaccine effectiveness data on Omicron are derived from the first Omicron subvariant, BA.1, which caused large waves of infection in many parts of the world within a short period of time. BA.1, however, was replaced by BA.2 within months, and later by BA.4 and BA.5 (BA.4/5). These later Omicron subvariants exhibited additional mutations in the spike protein of the virus, leading to speculation that they might result in even lower vaccine effectiveness. To address this question, the World Health Organization hosted a virtual meeting on December 6, 2022, to review available evidence for vaccine effectiveness against the major Omicron subvariants up to that date. Data were presented from South Africa, the United Kingdom, the United States, and Canada, as well as the results of a review and meta-regression of studies that evaluated the duration of the vaccine effectiveness for multiple Omicron subvariants. Despite heterogeneity of results and wide confidence intervals in some studies, the majority of studies showed vaccine effectiveness tended to be lower against BA.2 and especially against BA.4/5, compared to BA.1, with perhaps faster waning against severe disease caused by BA.4/5 after a booster dose. The interpretation of these results was discussed and both immunological factors (i.e., more immune escape with BA.4/5) and methodological issues (e.g., biases related to differences in the timing of subvariant circulation) were possible explanations for the findings. COVID-19 vaccines still provide some protection against infection and symptomatic disease from all Omicron subvariants for at least several months, with greater and more durable protection against severe disease.
2021 年 11 月出现的 SARS-CoV-2 奥密克戎关切变异株表现出明显的免疫逃逸,导致针对 SARS-CoV-2 感染和有症状疾病的疫苗效力降低。大多数关于奥密克戎的疫苗效力数据来自奥密克戎的第一个子变体 BA.1,它在短时间内在世界许多地区引发了大量感染。然而,BA.1 在几个月内被 BA.2 取代,随后被 BA.4 和 BA.5(BA.4/5)取代。这些后来的奥密克戎子变体在病毒的刺突蛋白中表现出额外的突变,导致人们推测它们可能导致疫苗效力更低。为了解决这个问题,世界卫生组织于 2022 年 12 月 6 日举行了一次虚拟会议,审查截至当日针对主要奥密克戎子变体的疫苗效力的现有证据。南非、英国、美国和加拿大的数据以及对评估多种奥密克戎子变体疫苗效力持续时间的研究进行的综述和荟萃回归的结果都进行了介绍。尽管一些研究的结果存在异质性且置信区间较宽,但大多数研究表明,与 BA.1 相比,BA.2 尤其是 BA.4/5 的疫苗效力较低,而在加强剂接种后,BA.4/5 引起的严重疾病的疫苗效力下降更快。对这些结果进行了讨论,并考虑了免疫因素(即 BA.4/5 具有更多的免疫逃逸)和方法学问题(例如,与子变体传播时间差异相关的偏倚)可能是这些发现的解释。至少在几个月内,COVID-19 疫苗仍然对所有奥密克戎子变体的感染和有症状疾病提供一定程度的保护,对严重疾病的保护作用更大且更持久。