老年人呼吸道合胞病毒疫苗研究进展

Q2 Medicine
Brian Torres, Julie M King, Robert M Richardson
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引用次数: 0

摘要

呼吸道合胞病毒(RSV)可引起严重疾病,特别是在老年人中,每年在65岁及以上的人群中导致数千人住院和死亡。2023年5月,美国食品和药物管理局(FDA)批准了两种疫苗Arexvy®(RSVPreF3)和Abrysvo®(RSVpreF),用于预防60岁及以上成人rsv相关下呼吸道疾病(LRTD)。2024年5月,FDA批准了第三种RSV疫苗mRESVIA®(mRNA-1345)。2024年6月,美国疾病控制与预防中心(CDC)更新了指南,建议所有75岁及以上的成年人以及60至74岁有严重疾病风险因素的人接种单剂RSV疫苗。临床试验表明,这三种疫苗在降低rsv相关发病率和死亡率方面都是安全有效的。目的回顾有关RSV疫苗在老年人中的安全性、有效性、耐受性和临床应用的文献。数据来源通过PubMed、美国临床试验注册中心和CDC资源确定的2021 - 2025年的主要文献,重点是随机临床试验和支持FDA批准的关键研究。Arexvy®(RSVPreF3)、Abrysvo®(RSVpreF)和mRESVIA®(mRNA-1345)在60岁及以上成人中显示出降低rsv相关LRTD和严重rsv相关LRTD风险的疗效。报告的不良反应包括注射部位疼痛、肌痛、疲劳和头痛。经济分析表明,这三种疫苗都具有潜在的成本效益。结论RSV具有显著的发病和死亡风险,尤其是在老年人中。Arexvy®(RSVPreF3)、Abrysvo®(RSVpreF)和mRESVIA®(mRNA-1345)已被证明可有效预防60岁及以上RSV引起的LRTD。药剂师在支持疾病预防控制中心的建议、教育患者和优化预防保健策略方面发挥着至关重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Review of Respiratory Syncytial Virus Vaccines in the Older Adult.

Background Respiratory syncytial virus (RSV) can cause severe illness, particularly in older adults, leading to thousands of hospitalizations and deaths annually among individuals aged 65 and older. In May 2023, the U.S. Food and Drug Administration (FDA) approved two vaccines, Arexvy® (RSVPreF3) and Abrysvo® (RSVpreF), for the prevention of RSV-related lower respiratory tract disease (LRTD) in adults aged 60 years and older. In May 2024, the FDA approved a third RSV vaccine, mRESVIA® (mRNA-1345). In June 2024, the Centers for Disease Control and Prevention (CDC) updated its guidance to recommend a single dose of an RSV vaccine for all adults aged 75 years and older, as well as those aged 60 to 74 years old with risk factors for severe disease. Clinical trials have demonstrated that all three vaccines are safe and effective in reducing RSV-related morbidity and mortality. Objective To review the literature describing the safety, efficacy, tolerability, and clinical application of RSV vaccines in older adults. Data Sources Primary literature identified through PubMed, the U.S. clinical trial registry, and CDC resources from 2021 to 2025, with an emphasis on randomized clinical trials and key studies supporting FDA approval. Data Synthesis Arexvy® (RSVPreF3), Abrysvo® (RSVpreF), and mRESVIA® (mRNA-1345) have demonstrated efficacy in reducing the risk of RSV-associated LRTD and severe RSV-associated LRTD in adults aged 60 years and older. Reported adverse effects include injection-site pain, myalgia, fatigue, and headaches. Economic analyses suggest that all three vaccines are potentially cost-effective. Conclusion RSV poses a significant risk of morbidity and mortality, especially in older adults. Arexvy® (RSVPreF3), Abrysvo® (RSVpreF), and mRESVIA® (mRNA-1345) have been shown to effectively prevent LRTD caused by RSV in individuals aged 60 and older. Pharmacists play a vital role in supporting CDC recommendations, educating patients and optimizing preventive health strategies.

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来源期刊
Senior Care Pharmacist
Senior Care Pharmacist PHARMACOLOGY & PHARMACY-
CiteScore
1.30
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0.00%
发文量
160
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