Wu Pan-Pan, Ding Fang-Rui
Department of Neonatology, Tianjin Central Hospital of Obstetrics and Gynecology, Tianjin 300100, China.
Tianjin Key Laboratory of Human Development and Reproductive Regulation, Tianjin 300100, China.
Vaccines (Basel). 2025 Apr 27;13(5):470. doi: 10.3390/vaccines13050470.
Respiratory syncytial virus (RSV) is the primary etiological agent responsible for lower respiratory tract infections (LRTIs) and hospitalizations among infants. Nirsevimab, a novel monoclonal antibody (mAb), offers sustained protection against RSV for a minimum of 5 months in neonates and young children. Extensive clinical trials and real-world evidence have demonstrated that nirsevimab significantly mitigates the incidence and severity of RSV infections in infants, while exhibiting favorable safety profiles and cost-effectiveness. Regulatory authorities in multiple countries have approved nirsevimab, and its implementation is progressively expanding across various healthcare settings. However, several critical issues require further attention. Specifically, a more in-depth investigation into the long-term efficacy and benefits of nirsevimab across diverse populations, particularly neonates, is essential. Additionally, accelerating the introduction and administration of nirsevimab in developing countries remains imperative. Thus, this review comprehensively summarizes the administration of nirsevimab in infants to facilitate its broader application.
呼吸道合胞病毒(RSV)是导致婴儿下呼吸道感染(LRTIs)和住院的主要病原体。Nirsevimab是一种新型单克隆抗体(mAb),可在新生儿和幼儿中为抵御RSV提供至少5个月的持续保护。广泛的临床试验和真实世界证据表明,Nirsevimab可显著降低婴儿RSV感染的发生率和严重程度,同时显示出良好的安全性和成本效益。多个国家的监管机构已批准Nirsevimab,其应用正在各种医疗环境中逐步扩大。然而,有几个关键问题需要进一步关注。具体而言,深入调查Nirsevimab在不同人群(尤其是新生儿)中的长期疗效和益处至关重要。此外,在发展中国家加快Nirsevimab的引入和给药仍然势在必行。因此,本综述全面总结了Nirsevimab在婴儿中的应用情况,以促进其更广泛的应用。