Influenza Vaccine Effectiveness and Progress Towards a Universal Influenza Vaccine

被引:1
|
作者
Cowling, Benjamin J. [1 ,2 ]
Okoli, George N. [1 ]
机构
[1] Univ Hong Kong, WHO Collaborating Ctr Infect Dis Epidemiol & Contr, Sch Publ Hlth, Pokfulam, Hong Kong, Peoples R China
[2] Hong Kong Sci & Technol Pk, Lab Data Discovery Hlth Ltd, Hong Kong, Peoples R China
关键词
TEST-NEGATIVE DESIGN; POLYSACCHARIDE VACCINE; UNITED-STATES; OLDER-ADULTS; VIRUS; EFFICACY; PROTECTION; LIVE; METAANALYSIS; SAFETY;
D O I
10.1007/s40265-024-02083-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:1013 / 1023
页数:11
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