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Pre-fusion F is absent on the surface of formalin-inactivated respiratory syncytial virus.甲醛灭活呼吸道合胞病毒表面不存在融合前F蛋白。
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A Recombinant Respiratory Syncytial Virus Vaccine Candidate Attenuated by a Low-Fusion F Protein Is Immunogenic and Protective against Challenge in Cotton Rats.一种由低融合F蛋白减毒的重组呼吸道合胞病毒候选疫苗具有免疫原性,并能保护棉鼠免受攻击。
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用于婴儿的呼吸道合胞病毒(RSV)疫苗的研发。

Development of respiratory syncytial virus (RSV) vaccines for infants.

作者信息

Gerretsen Hannah E, Sande Charles J

机构信息

Oxford Vaccine Group, Department of Paediatrics, and the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, University of Oxford, Oxford OX3 7LE, UK.

Oxford Vaccine Group, Department of Paediatrics, and the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, University of Oxford, Oxford OX3 7LE, UK; KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.

出版信息

J Infect. 2017 Jun;74 Suppl 1(Suppl 1):S143-S146. doi: 10.1016/S0163-4453(17)30205-0.

DOI:10.1016/S0163-4453(17)30205-0
PMID:28646954
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7613510/
Abstract

2017 will mark the 60 anniversary since the first isolation of RSV in children. In spite of concerted efforts over all these years, the goal of developing an effective vaccine against paediatric RSV disease has remained elusive. One of the main hurdles standing in the way of an effective vaccine is the fact that the age incidence of severe disease peaks within the first 3 months of life, providing limited opportunity for intervention. In addition to this complexity, the spectre of failed historical vaccines, which increased the risk of illness and death upon subsequent natural infection, has substantially increased the safety criteria against which modern vaccines will be assessed. This review traces the history of RSV vaccine development for young infants and analyses the potential reasons for the failure of historic vaccines. It also discusses recent breakthroughs in vaccine antigen design and the progressive evolution of platforms for the delivery of these antigens to seronegative infants.

摘要

2017年将是首次从儿童体内分离出呼吸道合胞病毒(RSV)60周年。尽管多年来人们齐心协力,但研发一种有效的抗小儿RSV疾病疫苗的目标仍难以实现。有效疫苗研发的主要障碍之一是,严重疾病的年龄发病率在生命的头3个月内达到峰值,这使得干预机会有限。除了这种复杂性之外,历史上疫苗研发失败的幽灵,即这些疫苗会增加后续自然感染时患病和死亡的风险,大大提高了评估现代疫苗的安全标准。本综述追溯了针对幼儿的RSV疫苗研发历史,并分析了历史疫苗失败的潜在原因。它还讨论了疫苗抗原设计方面的最新突破以及将这些抗原递送至血清阴性婴儿的平台的逐步发展。