Review and Update of Active and Passive Immunization Against Respiratory Syncytial Virus.

IF 5.4 2区 医学 Q1 IMMUNOLOGY
Charl Verwey, Shabir A Madhi
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引用次数: 3

Abstract

Respiratory syncytial virus (RSV) is the most common cause of lower respiratory tract infection (LRTI) in children, causing approximately 3.6 million hospitalizations per year, and has been associated with long-term pulmonary sequelae for up to 30 years after infection, yet preventative strategies and active treatment options remain elusive. The associated morbidity and healthcare related costs could be decreased substantially with the development of these much-needed medications. After an initial false start in the development of an RSV vaccine, gradual progress is now being made with the development of multiple vaccine candidates using numerous different mechanisms of action. Furthermore, nirsevimab, a new monoclonal antibody for the prevention of RSV, has recently been registered in the European Union. New novel treatments for RSV infection are also in the pipeline, which would provide the clinician with much needed ammunition in the management of the acute disease. The next few years have the potential to change the landscape of LRTI forever through the prevention and management of RSV LRTI and thereby decrease the mortality and morbidity associated with it. In this review, we discuss these new approaches, current research, and clinical trials in monoclonal antibody and vaccine development against RSV.

呼吸道合胞病毒主动免疫和被动免疫研究进展。
呼吸道合胞病毒(RSV)是儿童下呼吸道感染(LRTI)的最常见原因,每年导致约360万人住院,并与感染后长达30年的长期肺部后遗症有关,但预防策略和积极的治疗方案仍然难以捉摸。随着这些急需的药物的开发,相关的发病率和保健相关费用可以大大降低。在最初研制RSV疫苗的过程中出现了错误的开端之后,目前正在逐步取得进展,开发出使用多种不同作用机制的多种候选疫苗。此外,用于预防RSV的新型单克隆抗体nirsevimab最近已在欧盟注册。针对呼吸道合胞病毒感染的新型治疗方法也在研发中,这将为临床医生提供治疗这种急性疾病急需的弹药。未来几年,通过预防和管理RSV下呼吸道感染,有可能永远改变下呼吸道感染的现状,从而降低与之相关的死亡率和发病率。在这篇综述中,我们讨论了这些新的方法,目前的研究和临床试验的单克隆抗体和疫苗开发抗RSV。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BioDrugs
BioDrugs 医学-免疫学
CiteScore
12.60
自引率
2.90%
发文量
50
审稿时长
>12 weeks
期刊介绍: An essential resource for R&D professionals and clinicians with an interest in biologic therapies. BioDrugs covers the development and therapeutic application of biotechnology-based pharmaceuticals and diagnostic products for the treatment of human disease. BioDrugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.
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