Killikelly April, Siu Winnie, Brousseau Nicholas
Public Health Agency of Canada, Centre for Immunization and Respiratory Infectious Diseases, Ottawa, ON.
School of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, ON.
Can Commun Dis Rep. 2025 Apr 3;51(4):113-118. doi: 10.14745/ccdr.v51i04a01. eCollection 2025 Apr.
Immunization programs for the prevention of respiratory syncytial virus (RSV) in infants have been available in Canada since the authorization of palivizumab in 2002. However, these programs have been limited to only those infants at highest risk for severe RSV disease. The authorization of new passive immunizing products to prevent RSV, including a new monoclonal antibody (nirsevimab) and a vaccine administered in pregnancy (RSV pre-fusion stabilized F protein; RSVpreF) offers the opportunity to prevent RSV in more Canadian infants. The objective of this article is to summarize guidance from the National Advisory Committee on Immunization (NACI) on the prevention of RSV in infants.
NACI established key policy questions and performed an evidence review and synthesis. NACI made evidence-based recommendations in consideration of the burden of illness to be prevented, safety and efficacy of the new immunizing products, economic evidence and ethics, equity, feasibility, and acceptability.
Nirsevimab and RSVpreF offer protection against severe outcomes of RSV disease, including hospitalization and intensive care unit admission. Nirsevimab protection may be slightly higher and may last longer than protection offered by RSVpreF. Nirsevimab and RSVpreF also have a similar frequency of adverse reactions for both pregnant and infant participants. The RSVpreF vaccine may increase the risk of severe local adverse events compared to placebo for pregnant recipients. In RSVpreF clinical trials, an imbalance was observed in late preterm birth between RSVpreF and placebo recipients. It is unclear whether there is a causal relation with the vaccine as the currently available data is inconclusive.
Based on new evidence, NACI recommends building towards a universal RSV immunization program for all infants. Currently, nirsevimab is preferred over RSVpreF. Program introduction could occur in stages depending on access to supply, cost effectiveness, and affordability of available options.
自2002年帕利珠单抗获批以来,加拿大就有预防婴儿呼吸道合胞病毒(RSV)的免疫规划。然而,这些规划仅限于那些患严重RSV疾病风险最高的婴儿。新的预防RSV的被动免疫产品获批,包括一种新型单克隆抗体(尼塞韦单抗)和一种孕期接种的疫苗(RSV预融合稳定F蛋白;RSVpreF),为在更多加拿大婴儿中预防RSV提供了机会。本文的目的是总结国家免疫咨询委员会(NACI)关于婴儿RSV预防的指南。
NACI确定了关键政策问题,并进行了证据审查和综合分析。NACI在考虑要预防的疾病负担、新免疫产品的安全性和有效性、经济证据以及伦理、公平性、可行性和可接受性的基础上提出了基于证据的建议。
尼塞韦单抗和RSVpreF可预防RSV疾病的严重后果,包括住院和入住重症监护病房。尼塞韦单抗的保护作用可能略高,且持续时间可能比RSVpreF提供的保护更长。尼塞韦单抗和RSVpreF对孕妇和婴儿参与者的不良反应发生率也相似。与安慰剂相比,RSVpreF疫苗可能会增加孕妇接受者发生严重局部不良事件的风险。在RSVpreF临床试验中,观察到RSVpreF和安慰剂接受者之间晚期早产存在失衡。由于目前可得的数据尚无定论,尚不清楚这是否与疫苗存在因果关系。
基于新证据,NACI建议朝着为所有婴儿建立通用的RSV免疫规划努力。目前,尼塞韦单抗比RSVpreF更受青睐。规划的引入可根据供应情况、成本效益和可用选项的可承受性分阶段进行。