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Seasonal influenza vaccination expands hemagglutinin-specific antibody breadth to older and future A/H3N2 viruses
被引:6
|作者:
Ertesvag, Nina Urke
[1
]
Cox, Rebecca Jane
[1
,2
]
Lartey, Sarah Larteley
[1
]
Mohn, Kristin G-, I
[1
,3
]
Brokstad, Karl Albert
[1
]
Trieu, Mai-Chi
[1
]
机构:
[1] Univ Bergen, Influenza Ctr, Dept Clin Sci, Bergen, Norway
[2] Haukeland Hosp, Dept Microbiol, Bergen, Norway
[3] Haukeland Hosp, Dept Med, Bergen, Norway
来源:
基金:
欧盟地平线“2020”;
关键词:
PROTECTION;
VACCINES;
METAANALYSIS;
INFECTION;
RESPONSES;
EFFICACY;
A(H3N2);
HISTORY;
DESIGN;
IMPACT;
D O I:
10.1038/s41541-022-00490-0
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
History of influenza A/H3N2 exposure, especially childhood infection, shape antibody responses after influenza vaccination and infection, but have not been extensively studied. We investigated the breadth and durability of influenza A/H3N2-specific hemagglutinin-inhibition antibodies after live-attenuated influenza vaccine in children (aged 3-17 years, n = 42), and after inactivated influenza vaccine or infection in adults (aged 22-61 years, n = 42) using 14 antigenically distinct A/H3N2 viruses circulating from 1968 to 2018. We found that vaccination and infection elicited cross-reactive antibody responses, predominantly directed against newer or future strains. Childhood H3-priming increased the breadth and magnitude of back-boosted A/H3N2-specific antibodies in adults. Broader and more durable A/H3N2-specific antibodies were observed in repeatedly vaccinated adults than in children and previously unvaccinated adults. Our findings suggest that early A/H3N2 exposure and frequent seasonal vaccination could increase the breadth and seropositivity of antibody responses, which may improve vaccine protection against future viruses.
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页数:10
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