Aglipay Mary, Maguire Jonathon L, Swayze Sarah, Tuite Ashleigh, Mamdani Muhammad, Keown-Stoneman Charles, Birken Catherine S, Kwong Jeffrey C
Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.
Open Forum Infect Dis. 2024 Dec 19;12(1):ofae718. doi: 10.1093/ofid/ofae718. eCollection 2025 Jan.
Data on mRNA-1273 (Moderna) vaccine effectiveness (VE) in children aged 6 months to 5 years are limited. The objectives of this study were to assess mRNA-1273 vaccine effectiveness against symptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and coronavirus disease 2019 (COVID-19)-related hospitalization among children aged 6 months to 5 years during the initial 5 months of the vaccination campaign rollout, as well as to determine whether VE varied by age group (6 months to <2 years vs 2 to 5 years).
We used a test-negative study with linked health administrative data in Ontario, Canada, to evaluate vaccine effectiveness of mRNA-1273 against symptomatic SARS-CoV-2 infection and COVID-19-related hospitalization from July 28 to December 31, 2022. Participants included symptomatic children aged 6 months to 5 years who were tested by real-time polymerase chain reaction. The primary outcome was symptomatic infection, and the secondary outcome was COVID-19-related hospitalization.
We included 572 test-positive cases and 3467 test-negative controls. Receipt of mRNA-1273 was associated with reduced symptomatic SARS-CoV-2 infection (VE, 90%; 95% CI, 53%-99%) and COVID-19-related hospitalization (VE, 82%; 95% CI, 4%-99%) ≥7 days after the second dose. We were unable to detect heterogeneity in VE across age groups.
Our findings suggest that mRNA-1273 vaccine effectiveness was initially strong against symptomatic SARS-CoV-2 infection and hospitalization in children aged 6 months to 5 years. Further research is needed to understand long-term effectiveness.
关于mRNA-1273(莫德纳)疫苗在6个月至5岁儿童中的有效性数据有限。本研究的目的是评估在疫苗接种活动开展的最初5个月期间,mRNA-1273疫苗对6个月至5岁儿童有症状的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染和2019冠状病毒病(COVID-19)相关住院治疗的有效性,以及确定有效性是否因年龄组(6个月至<2岁与2至5岁)而异。
我们采用了一项与加拿大安大略省卫生行政数据相关联的检测阴性研究,以评估mRNA-1273在2022年7月28日至12月31日期间对有症状的SARS-CoV-2感染和COVID-19相关住院治疗的疫苗有效性。参与者包括通过实时聚合酶链反应检测的6个月至5岁有症状儿童。主要结局是有症状感染,次要结局是COVID-19相关住院治疗。
我们纳入了572例检测阳性病例和3467例检测阴性对照。在第二剂疫苗接种≥7天后,接种mRNA-1273与有症状的SARS-CoV-2感染减少(疫苗有效性,90%;95%置信区间,53%-99%)和COVID-19相关住院治疗减少(疫苗有效性,82%;95%置信区间,4%-99%)相关。我们未能检测到各年龄组疫苗有效性的异质性。
我们的研究结果表明,mRNA-1273疫苗在最初对6个月至5岁儿童有症状的SARS-CoV-2感染和住院治疗的有效性较强。需要进一步研究以了解长期有效性。