Emergent variant modeling of the serological repertoire to norovirus in young children

被引:7
|
作者
C. Lindesmith, Lisa [1 ]
Brewer-Jensen, Paul D. [1 ]
Conard, Helen [1 ,8 ]
O'Reilly, Kathleen M. [2 ,3 ]
Mallory, Michael L. [1 ]
Kelly, Daniel [4 ]
Willams, Rachel [5 ,6 ]
Edmunds, W. John [2 ,3 ]
Allen, David J. [4 ]
Bruer, Judit [5 ,7 ]
Baric, Ralph S. [1 ]
机构
[1] Univ North Carolina Chapel Hill, Dept Epidemiol, Chapel Hill, NC 27599 USA
[2] London Sch Hygiene & Trop Med, Ctr Math Modelling Infect Dis, London WC1EW 7HT, England
[3] London Sch Hygiene & Trop Med, Dept Infect Dis Epidemiol, London WC1EW 7HT, England
[4] London Sch Hyg & Trop Med, Fac Infect & Trop Dis, Dept Infect Biol, London WC1E 7HT, England
[5] UCL, UCL Great Ormond St Inst Child Hlth, Dept Infect Immun & Inflammat, London WC1N 1EH, England
[6] UCL, UCL Great Ormond St Inst Child Hlth, Dept Genet & Genom Med, London WC1N1EH, England
[7] Great Ormond St Hosp Children NHS Fdn Trust, Dept Microbiol, London WC1N 3JH, England
[8] Univ Coll Cork, Dept Microbiol, Cork T12K8AF, Ireland
基金
英国惠康基金;
关键词
UPDATED SYSTEMATIC ANALYSIS; AFFINITY MATURATION; MONOCLONAL-ANTIBODY; VIRUS-INFECTION; NATIONAL CAUSES; VACCINE; GASTROENTERITIS; STRAIN; PROTECTION; INFLUENZA;
D O I
10.1016/j.xcrm.2023.100954
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human norovirus is the leading cause of acute gastroenteritis. Young children and the elderly bear the great-est burden of disease, representing more than 200,000 deaths annually. Infection prevalence peaks at younger than 2 years and is driven by novel GII.4 variants that emerge and spread globally. Using a surrogate neutralization assay, we characterize the evolution of the serological neutralizing antibody (nAb) landscape in young children as they transition between sequential GII.4 pandemic variants. Following upsurge of the replacement variant, antigenic cartography illustrates remodeling of the nAb landscape to the new variant accompanied by improved nAb titer. However, nAb relative avidity remains focused on the preceding variant. These data support immune imprinting as a mechanism of immune evasion and GII.4 virus persistence across a population. Understanding the complexities of immunity to rapidly evolving and co-circulating viral variants, like those of norovirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV2), and dengue viruses, will fundamentally inform vaccine design for emerging pathogens.
引用
收藏
页数:18
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