Targeting neuraminidase: the next frontier for broadly protective influenza vaccines

被引:8
|
作者
Wu, Nicholas C. [1 ,2 ,3 ,4 ]
Ellebedy, Ali H. [5 ,6 ,7 ]
机构
[1] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
[2] Univ Illinois, Ctr Biophys & Quantitat Biol, Urbana, IL 61801 USA
[3] Univ Illinois, Carl R Woese Inst Genom Biol, Urbana, IL 61801 USA
[4] Univ Illinois, Carle Illinois Coll Med, Urbana, IL 61801 USA
[5] Washington Univ, Dept Pathol & Immunol, Sch Med, St Louis, MO 63130 USA
[6] Washington Univ, Ctr Vaccines & Immun Microbial Pathogens, Sch Med, St Louis, MO 63110 USA
[7] Washington Univ, Andrew M & Jane M Bursky Ctr Human Immunol, Immunotherapy Programs, Sch Med, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
VIRUS NEURAMINIDASE; ANTIBODY-RESPONSES; HEMAGGLUTININ-STEM; CONSERVED EPITOPES; IMMUNE-RESPONSE; GLOBULAR HEAD; PANDEMIC H1N1; ACTIVE-SITE; GLYCOPROTEIN; SUPPLEMENTATION;
D O I
10.1016/j.it.2023.11.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Current seasonal influenza vaccines, which mainly target hemagglutinin (HA), require annual updates due to the continuous antigenic drift of the influenza virus. Developing an influenza vaccine with increased breadth of protection will have significant public health benefits. The recent discovery of broadly protective antibodies to neuraminidase (NA) has provided important insights into developing a universal influenza vaccine, either by improving seasonal influenza vaccines or designing novel immunogens. However, further in-depth molecular characterizations of NA antibody responses are warranted to fully leverage broadly protective NA antibodies for influenza vaccine designs. Overall, we posit that focusing on NA for influenza vaccine development is synergistic with existing efforts targeting HA, and may represent a cost-effective approach to generating a broadly protective influenza vaccine.
引用
收藏
页码:11 / 19
页数:9
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