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A new class of highly potent, broadly neutralizing antibodies isolated from viremic patients infected with dengue virus

Identifieur interne : 001C32 ( Pmc/Curation ); précédent : 001C31; suivant : 001C33

A new class of highly potent, broadly neutralizing antibodies isolated from viremic patients infected with dengue virus

Auteurs : Wanwisa Dejnirattisai [Royaume-Uni] ; Wiyada Wongwiwat [Royaume-Uni] ; Sunpetchuda Supasa [Royaume-Uni, Thaïlande] ; Xiaokang Zhang [France] ; Xinghong Dai [États-Unis] ; Alexander Rouvinski [France] ; Amonrat Jumnainsong [Royaume-Uni, Thaïlande] ; Carolyn Edwards [Royaume-Uni] ; Nguyen Than Ha Quyen [Viêt Nam] ; Thaneeya Duangchinda [Thaïlande] ; Jonathan M. Grimes [Royaume-Uni] ; Wen-Yang Tsai [États-Unis] ; Chih-Yun Lai [États-Unis] ; Wei-Kung Wang [États-Unis] ; Prida Malasit [Thaïlande] ; Jeremy Farrar [Viêt Nam] ; Cameron P. Simmons [Viêt Nam, Australie] ; Z Hong Zhou [États-Unis] ; Felix A. Rey [France] ; Juthathip Mongkolsapaya [Royaume-Uni, Thaïlande] ; Gavin R. Screaton [Royaume-Uni]

Source :

RBID : PMC:4445969

Abstract

Dengue is a rapidly emerging, mosquito-borne viral infection, with an estimated 400 million infections occurring annually. To gain insight into dengue immunity, we characterized 145 human monoclonal antibodies (mAbs) and identified a previously unknown epitope, the envelope dimer epitope (EDE), that bridges two envelope protein subunits that make up the 90 repeating dimers on the mature virion. The mAbs to EDE were broadly reactive across the dengue serocomplex and fully neutralized virus produced in either insect cells or primary human cells, with 50% neutralization in the low picomolar range. Our results provide a path to a subunit vaccine against dengue virus and have implications for the design and monitoring of future vaccine trials in which the induction of antibody to the EDE should be prioritized.


Url:
DOI: 10.1038/ni.3058
PubMed: 25501631
PubMed Central: 4445969

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PMC:4445969

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<name sortKey="Wang, Wei Kung" sort="Wang, Wei Kung" uniqKey="Wang W" first="Wei-Kung" last="Wang">Wei-Kung Wang</name>
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<name sortKey="Malasit, Prida" sort="Malasit, Prida" uniqKey="Malasit P" first="Prida" last="Malasit">Prida Malasit</name>
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<name sortKey="Zhou, Z Hong" sort="Zhou, Z Hong" uniqKey="Zhou Z" first="Z Hong" last="Zhou">Z Hong Zhou</name>
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<name sortKey="Mongkolsapaya, Juthathip" sort="Mongkolsapaya, Juthathip" uniqKey="Mongkolsapaya J" first="Juthathip" last="Mongkolsapaya">Juthathip Mongkolsapaya</name>
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<wicri:regionArea>Medical Biotechnology Unit, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathumthani</wicri:regionArea>
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<name sortKey="Zhou, Z Hong" sort="Zhou, Z Hong" uniqKey="Zhou Z" first="Z Hong" last="Zhou">Z Hong Zhou</name>
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<nlm:aff id="A6">Department of Microbiology, Immunology and Molecular Genetics and California NanoSystems Institute, University of California Los Angeles, Los Angeles, California, USA</nlm:aff>
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<wicri:regionArea>Department of Microbiology, Immunology and Molecular Genetics and California NanoSystems Institute, University of California Los Angeles, Los Angeles, California</wicri:regionArea>
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<name sortKey="Rey, Felix A" sort="Rey, Felix A" uniqKey="Rey F" first="Felix A" last="Rey">Felix A. Rey</name>
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<nlm:aff id="A4">Institut Pasteur, Département de Virologie, Unité de Virologie Structurale, Paris, France</nlm:aff>
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<series>
<title level="j">Nature immunology</title>
<idno type="ISSN">1529-2908</idno>
<idno type="eISSN">1529-2916</idno>
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<div type="abstract" xml:lang="en">
<p id="P1">Dengue is a rapidly emerging, mosquito-borne viral infection, with an estimated 400 million infections occurring annually. To gain insight into dengue immunity, we characterized 145 human monoclonal antibodies (mAbs) and identified a previously unknown epitope, the envelope dimer epitope (EDE), that bridges two envelope protein subunits that make up the 90 repeating dimers on the mature virion. The mAbs to EDE were broadly reactive across the dengue serocomplex and fully neutralized virus produced in either insect cells or primary human cells, with 50% neutralization in the low picomolar range. Our results provide a path to a subunit vaccine against dengue virus and have implications for the design and monitoring of future vaccine trials in which the induction of antibody to the EDE should be prioritized.</p>
</div>
</front>
</TEI>
<pmc article-type="research-article">
<pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
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<front>
<journal-meta>
<journal-id journal-id-type="nlm-journal-id">100941354</journal-id>
<journal-id journal-id-type="pubmed-jr-id">21750</journal-id>
<journal-id journal-id-type="nlm-ta">Nat Immunol</journal-id>
<journal-id journal-id-type="iso-abbrev">Nat. Immunol.</journal-id>
<journal-title-group>
<journal-title>Nature immunology</journal-title>
</journal-title-group>
<issn pub-type="ppub">1529-2908</issn>
<issn pub-type="epub">1529-2916</issn>
</journal-meta>
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<article-id pub-id-type="pmid">25501631</article-id>
<article-id pub-id-type="pmc">4445969</article-id>
<article-id pub-id-type="doi">10.1038/ni.3058</article-id>
<article-id pub-id-type="manuscript">NIHMS692004</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>A new class of highly potent, broadly neutralizing antibodies isolated from viremic patients infected with dengue virus</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Dejnirattisai</surname>
<given-names>Wanwisa</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Wongwiwat</surname>
<given-names>Wiyada</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Supasa</surname>
<given-names>Sunpetchuda</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
<xref ref-type="aff" rid="A2">2</xref>
<xref ref-type="aff" rid="A3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhang</surname>
<given-names>Xiaokang</given-names>
</name>
<xref ref-type="aff" rid="A4">4</xref>
<xref ref-type="aff" rid="A5">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Dai</surname>
<given-names>Xinghong</given-names>
</name>
<xref ref-type="aff" rid="A6">6</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rouvinski</surname>
<given-names>Alexander</given-names>
</name>
<xref ref-type="aff" rid="A4">4</xref>
<xref ref-type="aff" rid="A5">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Jumnainsong</surname>
<given-names>Amonrat</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
<xref ref-type="aff" rid="A7">7</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Edwards</surname>
<given-names>Carolyn</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Quyen</surname>
<given-names>Nguyen Than Ha</given-names>
</name>
<xref ref-type="aff" rid="A8">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Duangchinda</surname>
<given-names>Thaneeya</given-names>
</name>
<xref ref-type="aff" rid="A9">9</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Grimes</surname>
<given-names>Jonathan M</given-names>
</name>
<xref ref-type="aff" rid="A10">10</xref>
<xref ref-type="aff" rid="A11">11</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tsai</surname>
<given-names>Wen-Yang</given-names>
</name>
<xref ref-type="aff" rid="A12">12</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Lai</surname>
<given-names>Chih-Yun</given-names>
</name>
<xref ref-type="aff" rid="A12">12</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wang</surname>
<given-names>Wei-Kung</given-names>
</name>
<xref ref-type="aff" rid="A12">12</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Malasit</surname>
<given-names>Prida</given-names>
</name>
<xref ref-type="aff" rid="A2">2</xref>
<xref ref-type="aff" rid="A9">9</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Farrar</surname>
<given-names>Jeremy</given-names>
</name>
<xref ref-type="aff" rid="A8">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Simmons</surname>
<given-names>Cameron P</given-names>
</name>
<xref ref-type="aff" rid="A8">8</xref>
<xref ref-type="aff" rid="A13">13</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhou</surname>
<given-names>Z Hong</given-names>
</name>
<xref ref-type="aff" rid="A6">6</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rey</surname>
<given-names>Felix A</given-names>
</name>
<xref ref-type="aff" rid="A4">4</xref>
<xref ref-type="aff" rid="A5">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mongkolsapaya</surname>
<given-names>Juthathip</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
<xref ref-type="aff" rid="A2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Screaton</surname>
<given-names>Gavin R</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
</contrib-group>
<aff id="A1">
<label>1</label>
Division of Immunology and Inflammation, Department of Medicine, Faculty of Medicine, Hammersmith Campus, Imperial College, London, UK</aff>
<aff id="A2">
<label>2</label>
Dengue Hemorrhagic Fever Research Unit, Office for Research and Development, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand</aff>
<aff id="A3">
<label>3</label>
Graduate Program in Immunology, Department of Immunology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand</aff>
<aff id="A4">
<label>4</label>
Institut Pasteur, Département de Virologie, Unité de Virologie Structurale, Paris, France</aff>
<aff id="A5">
<label>5</label>
CNRS UMR 3569 Virologie, Paris, France</aff>
<aff id="A6">
<label>6</label>
Department of Microbiology, Immunology and Molecular Genetics and California NanoSystems Institute, University of California Los Angeles, Los Angeles, California, USA</aff>
<aff id="A7">
<label>7</label>
The Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand</aff>
<aff id="A8">
<label>8</label>
Oxford University Clinical Research Unit, Wellcome Trust Major Overseas Program, Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam</aff>
<aff id="A9">
<label>9</label>
Medical Biotechnology Unit, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathumthani, Thailand</aff>
<aff id="A10">
<label>10</label>
Division of Structural Biology and Oxford Protein Production Facility, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK</aff>
<aff id="A11">
<label>11</label>
Science Division, Diamond Light Source, Diamond House, Harwell Science and Innovation Campus, Didcot, Oxfordshire, UK</aff>
<aff id="A12">
<label>12</label>
Department of Tropical Medicine, Medical Microbiology and Pharmacology, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, Hawaii, USA</aff>
<aff id="A13">
<label>13</label>
Department of Microbiology and Immunology, University of Melbourne, Carlton, Victoria, Australia</aff>
<author-notes>
<corresp id="CR1">Correspondence should be addressed to G.R.S. (
<email>g.screaton@imperial.ac.uk</email>
) or J.M. (
<email>j.mongkolsapaya@imperial.ac.uk</email>
).</corresp>
</author-notes>
<pub-date pub-type="nihms-submitted">
<day>20</day>
<month>5</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epub">
<day>15</day>
<month>12</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="ppub">
<month>2</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>01</day>
<month>8</month>
<year>2015</year>
</pub-date>
<volume>16</volume>
<issue>2</issue>
<fpage>170</fpage>
<lpage>177</lpage>
<pmc-comment>elocation-id from pubmed: 10.1038/ni.3058</pmc-comment>
<permissions>
<copyright-statement>© 2015 Nature America, Inc. All rights reserved.</copyright-statement>
<copyright-year>2015</copyright-year>
<license license-type="permissions-link">
<license-p>Reprints and permissions information is available online at
<ext-link ext-link-type="uri" xlink:href="http://www.nature.com/reprints/index.html">http://www.nature.com/reprints/index.html</ext-link>
.</license-p>
</license>
</permissions>
<abstract>
<p id="P1">Dengue is a rapidly emerging, mosquito-borne viral infection, with an estimated 400 million infections occurring annually. To gain insight into dengue immunity, we characterized 145 human monoclonal antibodies (mAbs) and identified a previously unknown epitope, the envelope dimer epitope (EDE), that bridges two envelope protein subunits that make up the 90 repeating dimers on the mature virion. The mAbs to EDE were broadly reactive across the dengue serocomplex and fully neutralized virus produced in either insect cells or primary human cells, with 50% neutralization in the low picomolar range. Our results provide a path to a subunit vaccine against dengue virus and have implications for the design and monitoring of future vaccine trials in which the induction of antibody to the EDE should be prioritized.</p>
</abstract>
</article-meta>
</front>
</pmc>
</record>

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