[Vaccination against respiratory syncytial virus (RSV)-For the protection of infants and older adults].

Innere Medizin (Heidelberg, Germany) Pub Date : 2024-11-01 Epub Date: 2024-10-25 DOI:10.1007/s00108-024-01795-z
Caitlin Pley, Beate Kampmann
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Abstract

Respiratory syncytial virus (RSV) is a frequent cause of respiratory infections in all age groups. Infections in infants and older adults frequently result in severe disease and complications. There is no specific antiviral treatment against RSV. The characterization of the structure of the fusion (F) protein in its immunogenic prefusion conformation has enabled the development of novel vaccines directed against the prefusion protein as the antigen. These include an adjuvanted monovalent vaccine (Arexvy) and a nonadjuvanted bivalent vaccine (Abrysvo). Both are approved and indicated for use in older adults, in whom they have been shown to be over 80% effective in the protection against symptomatic RSV infections and associated lower respiratory tract diseases. Abrysvo is approved for use in pregnancy to protect the newborn through the transplacental transfer of high-titer maternal antibodies. The vaccine has been shown to have an efficacy of over 80% in the first 3 months of life to protect the infant from severe RSV-associated lower respiratory disease but slightly deceases after an age of 6 months. The clinical studies demonstrated the safety of the vaccines in both adults and pregnant women. The rate of undesired side effects was low in all studies and severe side effects were very rare. The new vaccines are efficacious new tools to prevent RSV-associated disease and complications in high-risk groups. For infants, an alternative strategy can be passive immunization with monoclonal antibodies, including the recently developed nirsevimab, which has also shown high efficacy.

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[呼吸道合胞病毒(RSV)疫苗接种--用于保护婴儿和老年人]。
呼吸道合胞病毒(RSV)是各年龄段人群呼吸道感染的常见病因。婴儿和老年人感染后常常会导致严重的疾病和并发症。目前还没有针对 RSV 的特效抗病毒疗法。融合(F)蛋白在其免疫原性前融合构象中的结构特征使人们能够开发出以前融合蛋白为抗原的新型疫苗。其中包括一种佐剂单价疫苗(Arexvy)和一种非佐剂双价疫苗(Abrysvo)。这两种疫苗均已获批并适用于老年人,在预防有症状的 RSV 感染和相关下呼吸道疾病方面,它们的有效率超过 80%。Abrysvo 已获准在孕期使用,通过高滴度母源抗体的胎盘转移来保护新生儿。研究表明,在婴儿出生后的头 3 个月,该疫苗对预防严重的 RSV 相关下呼吸道疾病的有效率超过 80%,但在 6 个月后,该疫苗的有效率会略有下降。临床研究表明,疫苗对成人和孕妇都是安全的。在所有研究中,不良副作用的发生率都很低,严重的副作用也非常罕见。新疫苗是预防高危人群 RSV 相关疾病和并发症的有效新工具。对于婴儿来说,另一种策略是使用单克隆抗体进行被动免疫,包括最近开发的 nirsevimab,它也显示出很高的疗效。
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