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  • 1
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-05-12
    Description: Influenza B virus is a human pathogen whose origin and possible reservoir in nature are not known. An influenza B virus was isolated from a naturally infected harbor seal (Phoca vitulina) and was found to be infectious to seal kidney cells in vitro. Sequence analyses and serology indicated that influenza virus B/Seal/Netherlands/1/99 is closely related to strains that circulated in humans 4 to 5 years earlier. Retrospective analyses of sera collected from 971 seals showed a prevalence of antibodies to influenza B virus in 2% of the animals after 1995 and in none before 1995. This animal reservoir, harboring influenza B viruses that have circulated in the past, may pose a direct threat to humans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Osterhaus, A D -- Rimmelzwaan, G F -- Martina, B E -- Bestebroer, T M -- Fouchier, R A -- HD 15527/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2000 May 12;288(5468):1051-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉National Influenza Center, Department of Virology, Erasmus University, Doctor Molewaterplein 50, 3015 GE Rotterdam, Netherlands.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10807575" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibodies, Viral/blood ; Cell Line ; Cells, Cultured ; Disease Reservoirs ; Dogs ; Enzyme-Linked Immunosorbent Assay ; Genes, Viral ; Hemagglutination Inhibition Tests ; Hemagglutinin Glycoproteins, Influenza Virus/genetics ; Humans ; Influenza B virus/classification/genetics/immunology/*isolation & purification ; Neutralization Tests ; Orthomyxoviridae Infections/epidemiology/*veterinary/virology ; Pharynx/virology ; Reverse Transcriptase Polymerase Chain Reaction ; Seals, Earless/*virology ; Viral Nonstructural Proteins/genetics ; Virus Shedding
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2008-04-19
    Description: Antigenic and genetic analysis of the hemagglutinin of approximately 13,000 human influenza A (H3N2) viruses from six continents during 2002-2007 revealed that there was continuous circulation in east and Southeast Asia (E-SE Asia) via a region-wide network of temporally overlapping epidemics and that epidemics in the temperate regions were seeded from this network each year. Seed strains generally first reached Oceania, North America, and Europe, and later South America. This evidence suggests that once A (H3N2) viruses leave E-SE Asia, they are unlikely to contribute to long-term viral evolution. If the trends observed during this period are an accurate representation of overall patterns of spread, then the antigenic characteristics of A (H3N2) viruses outside E-SE Asia may be forecast each year based on surveillance within E-SE Asia, with consequent improvements to vaccine strain selection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Russell, Colin A -- Jones, Terry C -- Barr, Ian G -- Cox, Nancy J -- Garten, Rebecca J -- Gregory, Vicky -- Gust, Ian D -- Hampson, Alan W -- Hay, Alan J -- Hurt, Aeron C -- de Jong, Jan C -- Kelso, Anne -- Klimov, Alexander I -- Kageyama, Tsutomu -- Komadina, Naomi -- Lapedes, Alan S -- Lin, Yi P -- Mosterin, Ana -- Obuchi, Masatsugu -- Odagiri, Takato -- Osterhaus, Albert D M E -- Rimmelzwaan, Guus F -- Shaw, Michael W -- Skepner, Eugene -- Stohr, Klaus -- Tashiro, Masato -- Fouchier, Ron A M -- Smith, Derek J -- DP1-OD000490-01/OD/NIH HHS/ -- MC_U117512723/Medical Research Council/United Kingdom -- Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2008 Apr 18;320(5874):340-6. doi: 10.1126/science.1154137.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Zoology, University of Cambridge, Cambridge, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18420927" target="_blank"〉PubMed〈/a〉
    Keywords: Antigenic Variation ; Asia/epidemiology ; Asia, Southeastern/epidemiology ; *Disease Outbreaks ; Europe/epidemiology ; Evolution, Molecular ; Forecasting ; Hemagglutinin Glycoproteins, Influenza Virus/genetics/*immunology ; Humans ; *Influenza A Virus, H3N2 Subtype/classification/genetics/immunology/isolation & ; purification ; Influenza Vaccines ; Influenza, Human/*epidemiology/virology ; North America/epidemiology ; Oceania ; Phylogeny ; Population Surveillance ; Seasons ; South America/epidemiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2012-06-23
    Description: Highly pathogenic avian influenza A/H5N1 virus can cause morbidity and mortality in humans but thus far has not acquired the ability to be transmitted by aerosol or respiratory droplet ("airborne transmission") between humans. To address the concern that the virus could acquire this ability under natural conditions, we genetically modified A/H5N1 virus by site-directed mutagenesis and subsequent serial passage in ferrets. The genetically modified A/H5N1 virus acquired mutations during passage in ferrets, ultimately becoming airborne transmissible in ferrets. None of the recipient ferrets died after airborne infection with the mutant A/H5N1 viruses. Four amino acid substitutions in the host receptor-binding protein hemagglutinin, and one in the polymerase complex protein basic polymerase 2, were consistently present in airborne-transmitted viruses. The transmissible viruses were sensitive to the antiviral drug oseltamivir and reacted well with antisera raised against H5 influenza vaccine strains. Thus, avian A/H5N1 influenza viruses can acquire the capacity for airborne transmission between mammals without recombination in an intermediate host and therefore constitute a risk for human pandemic influenza.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Herfst, Sander -- Schrauwen, Eefje J A -- Linster, Martin -- Chutinimitkul, Salin -- de Wit, Emmie -- Munster, Vincent J -- Sorrell, Erin M -- Bestebroer, Theo M -- Burke, David F -- Smith, Derek J -- Rimmelzwaan, Guus F -- Osterhaus, Albert D M E -- Fouchier, Ron A M -- DP1-OD000490-01/OD/NIH HHS/ -- HHSN266200700010C/PHS HHS/ -- New York, N.Y. -- Science. 2012 Jun 22;336(6088):1534-41. doi: 10.1126/science.1213362.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Virology, Erasmus Medical Center, Rotterdam, The Netherlands.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22723413" target="_blank"〉PubMed〈/a〉
    Keywords: Air Microbiology ; Amino Acid Substitution ; Animals ; Antiviral Agents/pharmacology ; Containment of Biohazards ; Disease Models, Animal ; Female ; *Ferrets ; Hemagglutinin Glycoproteins, Influenza ; Virus/chemistry/genetics/immunology/metabolism ; Humans ; Immune Sera ; Influenza A Virus, H5N1 Subtype/drug effects/*genetics/*pathogenicity/physiology ; Influenza in Birds/epidemiology/virology ; Influenza, Human/epidemiology/transmission/*virology ; Molecular Sequence Data ; Mutagenesis, Site-Directed ; Mutation ; Orthomyxoviridae Infections/transmission/*virology ; Oseltamivir/pharmacology ; Pandemics ; Poultry ; RNA Replicase/chemistry/genetics ; Reassortant Viruses/pathogenicity ; Receptors, Virus/metabolism ; Respiratory System/*virology ; Reverse Genetics ; Serial Passage ; Sialic Acids/metabolism ; Viral Proteins/chemistry/genetics ; Virulence ; Virus Replication ; Virus Shedding
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2013-11-23
    Description: The molecular basis of antigenic drift was determined for the hemagglutinin (HA) of human influenza A/H3N2 virus. From 1968 to 2003, antigenic change was caused mainly by single amino acid substitutions, which occurred at only seven positions in HA immediately adjacent to the receptor binding site. Most of these substitutions were involved in antigenic change more than once. Equivalent positions were responsible for the recent antigenic changes of influenza B and A/H1N1 viruses. Substitution of a single amino acid at one of these positions substantially changed the virus-specific antibody response in infected ferrets. These findings have potentially far-reaching consequences for understanding the evolutionary mechanisms that govern influenza viruses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koel, Bjorn F -- Burke, David F -- Bestebroer, Theo M -- van der Vliet, Stefan -- Zondag, Gerben C M -- Vervaet, Gaby -- Skepner, Eugene -- Lewis, Nicola S -- Spronken, Monique I J -- Russell, Colin A -- Eropkin, Mikhail Y -- Hurt, Aeron C -- Barr, Ian G -- de Jong, Jan C -- Rimmelzwaan, Guus F -- Osterhaus, Albert D M E -- Fouchier, Ron A M -- Smith, Derek J -- DP1-OD000490-01/OD/NIH HHS/ -- HHSN266200700010C/PHS HHS/ -- New York, N.Y. -- Science. 2013 Nov 22;342(6161):976-9. doi: 10.1126/science.1244730.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Viroscience, Erasmus MC, 3015GE Rotterdam, Netherlands.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24264991" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution/genetics/immunology ; Antigens, Viral/genetics/*immunology ; Binding Sites/genetics ; *Evolution, Molecular ; Hemagglutinin Glycoproteins, Influenza Virus/genetics/*immunology ; Humans ; Influenza A Virus, H3N2 Subtype/genetics/*immunology ; Mutation
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2004-06-26
    Description: The antigenic evolution of influenza A (H3N2) virus was quantified and visualized from its introduction into humans in 1968 to 2003. Although there was remarkable correspondence between antigenic and genetic evolution, significant differences were observed: Antigenic evolution was more punctuated than genetic evolution, and genetic change sometimes had a disproportionately large antigenic effect. The method readily allows monitoring of antigenic differences among vaccine and circulating strains and thus estimation of the effects of vaccination. Further, this approach offers a route to predicting the relative success of emerging strains, which could be achieved by quantifying the combined effects of population level immune escape and viral fitness on strain evolution.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Smith, Derek J -- Lapedes, Alan S -- de Jong, Jan C -- Bestebroer, Theo M -- Rimmelzwaan, Guus F -- Osterhaus, Albert D M E -- Fouchier, Ron A M -- New York, N.Y. -- Science. 2004 Jul 16;305(5682):371-6. Epub 2004 Jun 24.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK. dsmith@zoo.cam.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15218094" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution ; Antigenic Variation ; *Evolution, Molecular ; *Genes, Viral ; Genetic Drift ; Genetic Variation ; Hemagglutination Inhibition Tests ; *Hemagglutinins, Viral/chemistry/genetics/immunology ; Humans ; Influenza A virus/*genetics/*immunology ; Influenza, Human/epidemiology/virology ; Molecular Sequence Data ; Mutagenesis, Site-Directed ; Mutation ; Seasons ; Virology/methods
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2013-08-09
    Description: Wild waterfowl form the main reservoir of influenza A viruses, from which transmission occurs directly or indirectly to various secondary hosts, including humans. Direct avian-to-human transmission has been observed for viruses of subtypes A(H5N1), A(H7N2), A(H7N3), A(H7N7), A(H9N2) and A(H10N7) upon human exposure to poultry, but a lack of sustained human-to-human transmission has prevented these viruses from causing new pandemics. Recently, avian A(H7N9) viruses were transmitted to humans, causing severe respiratory disease and deaths in China. Because transmission via respiratory droplets and aerosols (hereafter referred to as airborne transmission) is the main route for efficient transmission between humans, it is important to gain an insight into airborne transmission of the A(H7N9) virus. Here we show that although the A/Anhui/1/2013 A(H7N9) virus harbours determinants associated with human adaptation and transmissibility between mammals, its airborne transmissibility in ferrets is limited, and it is intermediate between that of typical human and avian influenza viruses. Multiple A(H7N9) virus genetic variants were transmitted. Upon ferret passage, variants with higher avian receptor binding, higher pH of fusion, and lower thermostability were selected, potentially resulting in reduced transmissibility. This A(H7N9) virus outbreak highlights the need for increased understanding of the determinants of efficient airborne transmission of avian influenza viruses between mammals.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819191/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3819191/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Richard, Mathilde -- Schrauwen, Eefje J A -- de Graaf, Miranda -- Bestebroer, Theo M -- Spronken, Monique I J -- van Boheemen, Sander -- de Meulder, Dennis -- Lexmond, Pascal -- Linster, Martin -- Herfst, Sander -- Smith, Derek J -- van den Brand, Judith M -- Burke, David F -- Kuiken, Thijs -- Rimmelzwaan, Guus F -- Osterhaus, Albert D M E -- Fouchier, Ron A M -- HHSN266200700010C/AI/NIAID NIH HHS/ -- HHSN266200700010C/PHS HHS/ -- England -- Nature. 2013 Sep 26;501(7468):560-3. doi: 10.1038/nature12476. Epub 2013 Aug 7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Viroscience, Erasmus Medical Center, 3015GE Rotterdam, The Netherlands.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23925116" target="_blank"〉PubMed〈/a〉
    Keywords: Air Microbiology ; Animals ; Birds/virology ; Cercopithecus aethiops ; Dogs ; Ferrets/*virology ; Genome, Viral/genetics ; Hemagglutinin Glycoproteins, Influenza Virus/chemistry ; Humans ; Influenza A virus/chemistry/classification/genetics/*pathogenicity ; Influenza in Birds/transmission/virology ; Influenza, Human/transmission/virology ; Madin Darby Canine Kidney Cells ; Models, Molecular ; Orthomyxoviridae Infections/*transmission/*virology ; Vero Cells
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 7
    Publication Date: 2006-04-22
    Description: Most emerging infectious diseases in humans originate from animal reservoirs; to contain and eradicate these diseases we need to understand how and why some pathogens become capable of crossing host species barriers. Influenza virus illustrates the interaction of factors that limit the transmission and subsequent establishment of an infection in a novel host species. Influenza species barriers can be categorized into virus-host interactions occurring within individuals and host-host interactions, either within or between species, that affect transmission between individuals. Viral evolution can help surmount species barriers, principally by affecting virus-host interactions; however, evolving the capability for sustained transmission in a new host species represents a major adaptive challenge because the number of mutations required is often large.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kuiken, Thijs -- Holmes, Edward C -- McCauley, John -- Rimmelzwaan, Guus F -- Williams, Catherine S -- Grenfell, Bryan T -- New York, N.Y. -- Science. 2006 Apr 21;312(5772):394-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Virology, Erasmus Medical Center, 3015 GE Rotterdam, Netherlands. t.kuiken@erasmusmc.nl〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16627737" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Birds ; Evolution, Molecular ; Humans ; Immunity, Innate ; Influenza A Virus, H5N1 Subtype/genetics/immunology/*pathogenicity/physiology ; Influenza A virus/genetics/immunology/*pathogenicity/physiology ; Influenza in Birds/transmission/virology ; Influenza, Human/epidemiology/immunology/*transmission/*virology ; Mutation ; Orthomyxoviridae Infections/immunology/transmission/veterinary/virology ; Poultry ; Reassortant Viruses ; Receptors, Virus/metabolism ; Recombination, Genetic ; Species Specificity ; Virus Replication ; Zoonoses
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 8
    Publication Date: 2006-03-25
    Description: Highly pathogenic avian influenza virus (H5N1) may cause severe lower respiratory tract (LRT) disease in humans. However, the LRT cells to which the virus attaches are unknown for both humans and other mammals. We show here that H5N1 virus attached predominantly to type II pneumocytes, alveolar macrophages, and nonciliated bronchiolar cells in the human LRT, and this pattern was most closely mirrored in cat and ferret tissues. These findings may explain, at least in part, the localization and severity of H5N1 viral pneumonia in humans. They also identify the cat and the ferret as suitable experimental animals based on this criterion.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉van Riel, Debby -- Munster, Vincent J -- de Wit, Emmie -- Rimmelzwaan, Guus F -- Fouchier, Ron A M -- Osterhaus, Ab D M E -- Kuiken, Thijs -- New York, N.Y. -- Science. 2006 Apr 21;312(5772):399. Epub 2006 Mar 23.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Virology, Erasmus Medical Center, 3015 GE Rotterdam, Netherlands.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16556800" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bronchi/cytology/*virology ; Cats ; Disease Models, Animal ; Epithelial Cells/virology ; Ferrets ; Humans ; Influenza A Virus, H5N1 Subtype/metabolism/*pathogenicity ; Influenza, Human/virology ; Macaca ; Macrophages, Alveolar/*virology ; Mice ; Orthomyxoviridae Infections/virology ; Pneumonia, Viral/virology ; Pulmonary Alveoli/cytology/*virology ; Receptors, Virus/metabolism ; Respiratory Mucosa/*virology ; Species Specificity ; Trachea/cytology/virology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
    Publication Date: 2009-07-04
    Description: The swine-origin A(H1N1) influenza virus that has emerged in humans in early 2009 has raised concerns about pandemic developments. In a ferret pathogenesis and transmission model, the 2009 A(H1N1) influenza virus was found to be more pathogenic than a seasonal A(H1N1) virus, with more extensive virus replication occurring in the respiratory tract. Replication of seasonal A(H1N1) virus was confined to the nasal cavity of ferrets, but the 2009 A(H1N1) influenza virus also replicated in the trachea, bronchi, and bronchioles. Virus shedding was more abundant from the upper respiratory tract for 2009 A(H1N1) influenza virus as compared with seasonal virus, and transmission via aerosol or respiratory droplets was equally efficient. These data suggest that the 2009 A(H1N1) influenza virus has the ability to persist in the human population, potentially with more severe clinical consequences.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Munster, Vincent J -- de Wit, Emmie -- van den Brand, Judith M A -- Herfst, Sander -- Schrauwen, Eefje J A -- Bestebroer, Theo M -- van de Vijver, David -- Boucher, Charles A -- Koopmans, Marion -- Rimmelzwaan, Guus F -- Kuiken, Thijs -- Osterhaus, Albert D M E -- Fouchier, Ron A M -- HHSN266200700010C/PHS HHS/ -- New York, N.Y. -- Science. 2009 Jul 24;325(5939):481-3. doi: 10.1126/science.1177127. Epub 2009 Jul 2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉National Influenza Center and Department of Virology, Erasmus Medical Center, 3015GE Rotterdam, The Netherlands.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19574348" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bronchi/virology ; Child, Preschool ; Disease Models, Animal ; Female ; Ferrets ; Humans ; Influenza A Virus, H1N1 Subtype/*pathogenicity ; Influenza, Human/pathology/transmission/*virology ; Orthomyxoviridae Infections/pathology/transmission/virology ; Respiratory System/virology ; Seasons ; Swine/virology ; Trachea/virology ; Virus Replication ; Virus Shedding
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 10
    Publication Date: 2014-11-22
    Description: We introduce the antibody landscape, a method for the quantitative analysis of antibody-mediated immunity to antigenically variable pathogens, achieved by accounting for antigenic variation among pathogen strains. We generated antibody landscapes to study immune profiles covering 43 years of influenza A/H3N2 virus evolution for 69 individuals monitored for infection over 6 years and for 225 individuals pre- and postvaccination. Upon infection and vaccination, titers increased broadly, including previously encountered viruses far beyond the extent of cross-reactivity observed after a primary infection. We explored implications for vaccination and found that the use of an antigenically advanced virus had the dual benefit of inducing antibodies against both advanced and previous antigenic clusters. These results indicate that preemptive vaccine updates may improve influenza vaccine efficacy in previously exposed individuals.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4246172/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4246172/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fonville, J M -- Wilks, S H -- James, S L -- Fox, A -- Ventresca, M -- Aban, M -- Xue, L -- Jones, T C -- Le, N M H -- Pham, Q T -- Tran, N D -- Wong, Y -- Mosterin, A -- Katzelnick, L C -- Labonte, D -- Le, T T -- van der Net, G -- Skepner, E -- Russell, C A -- Kaplan, T D -- Rimmelzwaan, G F -- Masurel, N -- de Jong, J C -- Palache, A -- Beyer, W E P -- Le, Q M -- Nguyen, T H -- Wertheim, H F L -- Hurt, A C -- Osterhaus, A D M E -- Barr, I G -- Fouchier, R A M -- Horby, P W -- Smith, D J -- 087982/Wellcome Trust/United Kingdom -- 089276/Wellcome Trust/United Kingdom -- DP1-OD000490-01/OD/NIH HHS/ -- HHSN266200700010C/PHS HHS/ -- HHSN272201400008C/PHS HHS/ -- MR/K021885/1/Medical Research Council/United Kingdom -- WT087982MA/Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2014 Nov 21;346(6212):996-1000. doi: 10.1126/science.1256427.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Pathogen Evolution, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK. World Health Organization (WHO) Collaborating Center for Modeling, Evolution, and Control of Emerging Infectious Diseases, Cambridge CB2 3EJ, UK. Department of Viroscience, Erasmus Medical Center, Rotterdam 3015 CE, Netherlands. ; Center for Pathogen Evolution, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK. World Health Organization (WHO) Collaborating Center for Modeling, Evolution, and Control of Emerging Infectious Diseases, Cambridge CB2 3EJ, UK. ; Oxford University Clinical Research Unit and Wellcome Trust Major Overseas Programme, Hanoi, Vietnam. ; Center for Pathogen Evolution, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK. ; WHO Collaborating Centre for Reference and Research on Influenza, Victorian Infectious Diseases Reference Laboratory at the Peter Doherty Institute for Infection and Immunity, Melbourne VIC 3000, Australia. ; National Institute of Hygiene and Epidemiology, Hanoi, Vietnam. ; Oxford University Museum of Natural History, Oxford OX1 3PW, UK. ; Insect Biomechanics Group, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK. ; Department of Viroscience, Erasmus Medical Center, Rotterdam 3015 CE, Netherlands. ; World Health Organization (WHO) Collaborating Center for Modeling, Evolution, and Control of Emerging Infectious Diseases, Cambridge CB2 3EJ, UK. Department of Veterinary Medicine, University of Cambridge, Cambridge CB3 0ES, UK. ; bobblewire.com, Saint Louis, MO 63112, USA. ; Abbott Laboratories, Weesp 1380 DA, Netherlands. ; Oxford University Clinical Research Unit and Wellcome Trust Major Overseas Programme, Hanoi, Vietnam. Nuffield Department of Clinical Medicine, Centre for Tropical Medicine, University of Oxford, Oxford OX3 7BN, UK. ; WHO Collaborating Centre for Reference and Research on Influenza, Victorian Infectious Diseases Reference Laboratory at the Peter Doherty Institute for Infection and Immunity, Melbourne VIC 3000, Australia. Melbourne School of Population and Global Health, University of Melbourne, Parkville VIC 3010, Australia. ; Center for Pathogen Evolution, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK. World Health Organization (WHO) Collaborating Center for Modeling, Evolution, and Control of Emerging Infectious Diseases, Cambridge CB2 3EJ, UK. Department of Viroscience, Erasmus Medical Center, Rotterdam 3015 CE, Netherlands. dsmith@zoo.cam.ac.uk.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25414313" target="_blank"〉PubMed〈/a〉
    Keywords: Antibodies, Viral/blood/*immunology ; Antigenic Variation/genetics/immunology ; Evolution, Molecular ; Humans ; Influenza A Virus, H3N2 Subtype/genetics/*immunology ; Influenza Vaccines/*immunology ; Influenza, Human/blood/*immunology/prevention & control ; *Vaccination
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    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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