Department of Population Medicine, Ontario Veterinary College, University of Guelph, Guelph, ON, Canada.
School of Public Health and Social Policy, Faculty of Human and Social Development, University of Victoria, Victoria, BC, Canada.
Front Public Health. 2023 Oct 24;11:1229716. doi: 10.3389/fpubh.2023.1229716. eCollection 2023.
The purpose of this systematic review was to report on the vaccine efficacy (VE) of three SARS-CoV-2 vaccines approved by Health Canada: Pfizer BioNTech, Moderna, and AstraZeneca. Four databases were searched for primary publications on population-level VE. Ninety-two publications matched the inclusion criteria, and the extracted data were separated by vaccine type: mRNA vaccines (Pfizer and Moderna) and the AstraZeneca vaccine. The median VE for PCR-positive patients and various levels of clinical disease was determined for the first and second doses of both vaccine types against multiple SARS-CoV-2 variants. The median VE for PCR-positive infections against unidentified variants from an mRNA vaccine was 64.5 and 89%, respectively, after one or two doses. The median VE for PCR-positive infections against unidentified variants from the AstraZeneca vaccine was 53.4 and 69.6%, respectively, after one or two doses. The median VE for two doses of mRNA for asymptomatic, symptomatic, and severe infection against unidentified variants was 85.5, 93.2, and 92.2%, respectively. The median VE for two doses of AstraZeneca for asymptomatic, symptomatic, and severe infection against unidentified variants was 69.7, 71, and 90.2%, respectively. Vaccine efficacy numerically increased from the first to the second dose, increased from the first 2 weeks to the second 2 weeks post-vaccination for both doses, but decreased after 4 months from the second dose. Vaccine efficacy did not differ by person's age.
本系统评价的目的是报告加拿大卫生部批准的三种 SARS-CoV-2 疫苗(辉瑞、莫德纳和阿斯利康)的疫苗效力(VE)。四个数据库被用于搜索人群 VE 的原始出版物。有 92 篇出版物符合纳入标准,并根据疫苗类型(mRNA 疫苗[辉瑞和莫德纳]和阿斯利康疫苗)将提取的数据分开。针对多种 SARS-CoV-2 变体,确定了第一剂和第二剂这两种疫苗类型对 PCR 阳性患者和不同程度临床疾病的 VE 中位数。在接种一剂或两剂疫苗后,针对未鉴定变异株,mRNA 疫苗对 PCR 阳性感染的 VE 中位数分别为 64.5%和 89%。在接种一剂或两剂疫苗后,针对未鉴定变异株,阿斯利康疫苗对 PCR 阳性感染的 VE 中位数分别为 53.4%和 69.6%。针对无症状、有症状和严重感染的两剂 mRNA 疫苗对未鉴定变异株的 VE 中位数分别为 85.5%、93.2%和 92.2%。针对无症状、有症状和严重感染的两剂阿斯利康疫苗对未鉴定变异株的 VE 中位数分别为 69.7%、71%和 90.2%。从第一剂到第二剂,疫苗效力数值增加,两剂接种后前两周至第二周增加,但第二剂接种后 4 个月后下降。疫苗效力不因接种者年龄而异。