Influenza B virus neuraminidase: a potential target for next-generation vaccines?

被引:9
|
作者
Do, Thi Hoai Thu [1 ]
Wheatley, Adam K. [1 ]
Kent, Stephen J. [1 ,2 ,3 ,4 ,5 ]
Koutsakos, Marios [1 ,6 ]
机构
[1] Univ Melbourne, Dept Microbiol & Immunol, Melbourne, Australia
[2] Peter Doherty Inst Infect & Immun, Melbourne, Australia
[3] Monash Univ, Melbourne Sexual Hlth Ctr, Melbourne, Australia
[4] Monash Univ, Alfred Hosp, Dept Infect Dis, Melbourne, Australia
[5] Monash Univ, Cent Clin Sch, Melbourne, Australia
[6] Univ Melbourne, Peter Doherty Inst Infect & Immun, Dept Microbiol & Immunol, Melbourne, Australia
基金
英国医学研究理事会;
关键词
Antibodies; influenza B virus; neuraminidase; universal vaccines; antigenic evolution; HUMAN-ANTIBODIES; ACTIVE-SITE; HEMAGGLUTININ; PROTECTION; RESISTANCE; SUPPLEMENTATION; OSELTAMIVIR; EVOLUTION; INFECTION; ANTIGENS;
D O I
10.1080/14760584.2023.2290691
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IntroductionInfluenza B viruses (IBV) cause a significant health and economic burden annually. Due to lower antigenic drift rate, less extensive antigenic diversity, and lack of animal reservoirs, the development of highly effective universal vaccines against IBV might be in reach. Current seasonal influenza vaccines are formulated to induce antibodies against the Hemagglutinin (HA) protein, but their effectiveness is reduced by mismatch between vaccine and circulating strains.Areas coveredGiven antibodies against the Neuraminidase (NA) have been associated with protection during influenza infection, there is considerable interest in the development of NA-based influenza vaccines. This review summarizes insights into the role of NA-based immunity against IBV and highlights knowledge gaps that should be addressed to inform the design of next-generation influenza B vaccines. We discuss how antibodies recognize broadly cross-reactive epitopes on the NA and the lack of understanding of IBV NA antigenic evolution which would benefit vaccine development in the future.Expert opinionDemonstrating NA antibodies as correlates of protection for IBV in humans would be paramount. Determining the extent of IBV NA antigenic evolution will be informative. Finally, it will be critical to determine optimal strategies for incorporating the appropriate NA antigens in existing clinically approved vaccine formulations.
引用
收藏
页码:39 / 48
页数:10
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