Antigenic sites in influenza H1 hemagglutinin display species-specific immunodominance

Hemagglutination inhibition (HI) titers are a major correlate of protection for influenza-related illness. The influenza virus hemagglutinin possesses antigenic sites that are the targets of HI active antibodies. Here, a panel of mutant viruses each lacking a classically defined antigenic site was c...

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Published inThe Journal of clinical investigation Vol. 128; no. 11; pp. 4992 - 4996
Main Authors Liu, Sean T H, Behzadi, Mohammad Amin, Sun, Weina, Freyn, Alec W, Liu, Wen-Chun, Broecker, Felix, Albrecht, Randy A, Bouvier, Nicole M, Simon, Viviana, Nachbagauer, Raffael, Krammer, Florian, Palese, Peter
Format Journal Article
LanguageEnglish
Published United States American Society for Clinical Investigation 01.11.2018
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Summary:Hemagglutination inhibition (HI) titers are a major correlate of protection for influenza-related illness. The influenza virus hemagglutinin possesses antigenic sites that are the targets of HI active antibodies. Here, a panel of mutant viruses each lacking a classically defined antigenic site was created to compare the species-specific immunodominance of the antigenic sites in a clinically relevant hemagglutinin. HI active antibodies of antisera from influenza virus-infected mice targeted sites Sb and Ca2. HI active antibodies of guinea pigs were not directed against any specific antigenic site, although trends were observed toward Sb, Ca2, and Sa. HI titers of antisera from infected ferrets were significantly affected by site Sa. HI active antibodies of adult humans followed yet another immunodominance pattern, in which sites Sb and Sa were immunodominant. When comparing the HI profiles among different species by antigenic cartography, animals and humans grouped separately. This study provides characterizations of the antibody-mediated immune responses against the head domain of a recent H1 hemagglutinin in animals and humans.
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Authorship note: MAB and WS contributed equally to this work.
ISSN:0021-9738
1558-8238
DOI:10.1172/JCI122895