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流感疫苗效力及通用流感疫苗的研发进展。

Influenza Vaccine Effectiveness and Progress Towards a Universal Influenza Vaccine.

机构信息

WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.

Laboratory of Data Discovery for Health Limited, Hong Kong Science and Technology Park, New Territories, Hong Kong Special Administrative Region, Hong Kong, China.

出版信息

Drugs. 2024 Sep;84(9):1013-1023. doi: 10.1007/s40265-024-02083-8. Epub 2024 Aug 21.

DOI:10.1007/s40265-024-02083-8
PMID:39167316
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11438668/
Abstract

At various times in recent decades, surges have occurred in optimism about the potential for universal influenza vaccines that provide strong, broad, and long-lasting protection and could substantially reduce the disease burden associated with seasonal influenza epidemics as well as the threat posed by pandemic influenza. Each year more than 500 million doses of seasonal influenza vaccine are administered around the world, with most doses being egg-grown inactivated subunit or split-virion vaccines. These vaccines tend to have moderate effectiveness against medically attended influenza for influenza A(H1N1) and influenza B, and somewhat lower for influenza A(H3N2) where differences between vaccine strains and circulating strains can occur more frequently due to antigenic drift and egg adaptations in the vaccine strains. Several enhanced influenza vaccine platforms have been developed including cell-grown antigen, the inclusion of adjuvants, or higher antigen doses, to improve immunogenicity and protection. During the COVID-19 pandemic there was unprecedented speed in development and roll-out of relatively new vaccine platforms, including mRNA vaccines and viral vector vaccines. These new platforms present opportunities to improve protection for influenza beyond existing products. Other approaches continue to be explored. Incremental improvements in influenza vaccine performance should be achievable in the short to medium term.

摘要

近几十年来的不同时期,人们对通用流感疫苗的潜力持乐观态度,认为通用流感疫苗能提供强大、广泛和持久的保护,并能大大减轻季节性流感流行和大流行性流感带来的疾病负担。每年,全球有超过 5 亿剂季节性流感疫苗,其中大多数是在鸡蛋中生长的灭活亚单位或分裂病毒疫苗。这些疫苗对甲型 H1N1 和乙型流感的医学上有症状的流感的有效性往往适中,而对甲型 H3N2 的有效性略低,因为疫苗株和流行株之间的差异由于抗原漂移和疫苗株中的鸡蛋适应性而更频繁地发生。已经开发了几种增强型流感疫苗平台,包括细胞生长抗原、佐剂的加入或更高的抗原剂量,以提高免疫原性和保护效果。在 COVID-19 大流行期间,相对较新的疫苗平台(包括 mRNA 疫苗和病毒载体疫苗)的开发和推出速度前所未有。这些新平台为流感提供了超越现有产品的保护机会。其他方法仍在探索中。在短期内到中期,流感疫苗的性能应该可以实现逐步提高。

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A chimeric haemagglutinin-based universal influenza virus vaccine boosts human cellular immune responses directed towards the conserved haemagglutinin stalk domain and the viral nucleoprotein.一种基于嵌合血凝素的通用流感病毒疫苗可增强针对保守血凝素茎域和病毒核蛋白的人体细胞免疫应答。
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