Pre-existing immunity with high neutralizing activity to 2009 pandemic H1N1 influenza virus in Shanghai population

Pre-existing immunity is an important factor countering the pandemic potential of an emerging influenza virus strain. Thus, studying of pre-existing immunity to the 2009 pandemic H1N1 virus (2009 H1N1) will advance our understanding of the pathogenesis and epidemiology of this emerging pathogen. In...

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Veröffentlicht in:PloS one 2013-03, Vol.8 (3), p.e58810-e58810
Hauptverfasser: Liu, Xiaoqing, Liu, Yuan, Zhang, Yanjun, Chen, Zhihui, Tang, Ziwei, Xu, Qingqiang, Wang, Yue, Zhao, Ping, Qi, Zhongtian
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creator Liu, Xiaoqing
Liu, Yuan
Zhang, Yanjun
Chen, Zhihui
Tang, Ziwei
Xu, Qingqiang
Wang, Yue
Zhao, Ping
Qi, Zhongtian
description Pre-existing immunity is an important factor countering the pandemic potential of an emerging influenza virus strain. Thus, studying of pre-existing immunity to the 2009 pandemic H1N1 virus (2009 H1N1) will advance our understanding of the pathogenesis and epidemiology of this emerging pathogen. In the present study, sera were collected from 486 individuals in a hospital in Shanghai, China, before the 2009 H1N1 influenza pandemic. The serum anti-hemagglutinins (HA) antibody, hemagglutination inhibition (HI) antibody and neutralizing antibody against the 2009 H1N1 were assayed. Among this population, 84.2%, 14.61% and 26.5% subjects possessed anti-HA antibody, HI antibody and neutralizing antibody, respectively. Although neutralizing antibody only existed in those sera with detectable anti-HA antibody, there was no obvious correlation between the titers of anti-HA and neutralizing antibody. However, the titers of anti-HA and neutralizing antibody against seasonal H1N1 virus were highly correlated. In the same population, there was no correlation between titers of neutralizing antibody against 2009 H1N1 and seasonal H1N1. DNA immunization performed on mice demonstrated that antibodies to the HA of 2009 pandemic and seasonal H1N1 influenza viruses were strain-specific and had no cross-neutralizing activity. In addition, the predicted conserved epitope in the HA of 2009 H1N1 and recently circulating seasonal H1N1 virus, GLFGAIAGFIE, was not an immunologically valid B-cell epitope. The data in this report are valuable for advancing our understanding of 2009 H1N1 influenza virus infection.
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Thus, studying of pre-existing immunity to the 2009 pandemic H1N1 virus (2009 H1N1) will advance our understanding of the pathogenesis and epidemiology of this emerging pathogen. In the present study, sera were collected from 486 individuals in a hospital in Shanghai, China, before the 2009 H1N1 influenza pandemic. The serum anti-hemagglutinins (HA) antibody, hemagglutination inhibition (HI) antibody and neutralizing antibody against the 2009 H1N1 were assayed. Among this population, 84.2%, 14.61% and 26.5% subjects possessed anti-HA antibody, HI antibody and neutralizing antibody, respectively. Although neutralizing antibody only existed in those sera with detectable anti-HA antibody, there was no obvious correlation between the titers of anti-HA and neutralizing antibody. However, the titers of anti-HA and neutralizing antibody against seasonal H1N1 virus were highly correlated. In the same population, there was no correlation between titers of neutralizing antibody against 2009 H1N1 and seasonal H1N1. DNA immunization performed on mice demonstrated that antibodies to the HA of 2009 pandemic and seasonal H1N1 influenza viruses were strain-specific and had no cross-neutralizing activity. In addition, the predicted conserved epitope in the HA of 2009 H1N1 and recently circulating seasonal H1N1 virus, GLFGAIAGFIE, was not an immunologically valid B-cell epitope. 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Thus, studying of pre-existing immunity to the 2009 pandemic H1N1 virus (2009 H1N1) will advance our understanding of the pathogenesis and epidemiology of this emerging pathogen. In the present study, sera were collected from 486 individuals in a hospital in Shanghai, China, before the 2009 H1N1 influenza pandemic. The serum anti-hemagglutinins (HA) antibody, hemagglutination inhibition (HI) antibody and neutralizing antibody against the 2009 H1N1 were assayed. Among this population, 84.2%, 14.61% and 26.5% subjects possessed anti-HA antibody, HI antibody and neutralizing antibody, respectively. Although neutralizing antibody only existed in those sera with detectable anti-HA antibody, there was no obvious correlation between the titers of anti-HA and neutralizing antibody. However, the titers of anti-HA and neutralizing antibody against seasonal H1N1 virus were highly correlated. 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Thus, studying of pre-existing immunity to the 2009 pandemic H1N1 virus (2009 H1N1) will advance our understanding of the pathogenesis and epidemiology of this emerging pathogen. In the present study, sera were collected from 486 individuals in a hospital in Shanghai, China, before the 2009 H1N1 influenza pandemic. The serum anti-hemagglutinins (HA) antibody, hemagglutination inhibition (HI) antibody and neutralizing antibody against the 2009 H1N1 were assayed. Among this population, 84.2%, 14.61% and 26.5% subjects possessed anti-HA antibody, HI antibody and neutralizing antibody, respectively. Although neutralizing antibody only existed in those sera with detectable anti-HA antibody, there was no obvious correlation between the titers of anti-HA and neutralizing antibody. However, the titers of anti-HA and neutralizing antibody against seasonal H1N1 virus were highly correlated. In the same population, there was no correlation between titers of neutralizing antibody against 2009 H1N1 and seasonal H1N1. DNA immunization performed on mice demonstrated that antibodies to the HA of 2009 pandemic and seasonal H1N1 influenza viruses were strain-specific and had no cross-neutralizing activity. In addition, the predicted conserved epitope in the HA of 2009 H1N1 and recently circulating seasonal H1N1 virus, GLFGAIAGFIE, was not an immunologically valid B-cell epitope. The data in this report are valuable for advancing our understanding of 2009 H1N1 influenza virus infection.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23527030</pmid><doi>10.1371/journal.pone.0058810</doi><tpages>e58810</tpages><oa>free_for_read</oa></addata></record>
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ispartof PloS one, 2013-03, Vol.8 (3), p.e58810-e58810
issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_1330889433
source MEDLINE; DOAJ Directory of Open Access Journals; Public Library of Science (PLoS); EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry
subjects Adolescent
Adult
Aged
Aged, 80 and over
Amino Acid Sequence
Animals
Antibodies
Antibodies, Neutralizing
Antibodies, Viral - blood
Antibodies, Viral - immunology
Antibody Specificity
Antigenic determinants
Binding sites
Biology
Cell Line
China
Correlation
Cross Reactions - immunology
Deoxyribonucleic acid
Disease control
Disease prevention
DNA
Epidemiology
Epitopes
Epitopes, B-Lymphocyte - chemistry
Epitopes, B-Lymphocyte - immunology
Evolution & development
Female
Health aspects
Hemagglutination inhibition
Hemagglutinin Glycoproteins, Influenza Virus - immunology
Hemagglutinins
Humans
Immunity
Immunization
Immunoglobulin G - blood
Immunoglobulin G - immunology
Immunoglobulins
Infections
Influenza
Influenza A Virus, H1N1 Subtype - immunology
Influenza viruses
Influenza, Human - epidemiology
Influenza, Human - immunology
Influenza, Human - prevention & control
Laboratories
Lymphocytes B
Male
Medicine
Mice
Middle Aged
Neutralization Tests
Neutralizing
Orthomyxoviridae
Pandemics
Pathogenesis
Plasmids
Population
Swine flu
Swine influenza
Vaccines
Viruses
Young Adult
title Pre-existing immunity with high neutralizing activity to 2009 pandemic H1N1 influenza virus in Shanghai population
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