Reservoir Host Immune Responses to Emerging Zoonotic Viruses
Identifieur interne : 000480 ( Ncbi/Merge ); précédent : 000479; suivant : 000481Reservoir Host Immune Responses to Emerging Zoonotic Viruses
Auteurs : Judith N. Mandl [États-Unis] ; Rafi Ahmed [États-Unis] ; Luis B. Barreiro [Canada] ; Peter Daszak [États-Unis] ; Jonathan H. Epstein [États-Unis] ; Herbert W. Virgin [États-Unis] ; Mark B. Feinberg [États-Unis]Source :
- Cell [ 0092-8674 ] ; 2014.
Abstract
Zoonotic viruses, such as HIV, Ebola virus, coronaviruses, influenza A viruses, hantaviruses, or henipaviruses, can result in profound pathology in humans. In contrast, populations of the reservoir hosts of zoonotic pathogens often appear to tolerate these infections with little evidence of disease. Why are viruses more dangerous in one species than another? Immunological studies investigating quantitative and qualitative differences in the host-virus equilibrium in animal reservoirs will be key to answering this question, informing new approaches for treating and preventing zoonotic diseases. Integrating an understanding of host immune responses with epidemiological, ecological, and evolutionary insights into viral emergence will shed light on mechanisms that minimize fitness costs associated with viral infection, facilitate transmission to other hosts, and underlie the association of specific reservoir hosts with multiple emerging viruses. Reservoir host studies provide a rich opportunity for elucidating fundamental immunological processes and their underlying genetic basis, in the context of distinct physiological and metabolic constraints that contribute to host resistance and disease tolerance.
Url:
DOI: 10.1016/j.cell.2014.12.003
PubMed: 25533784
PubMed Central: 4390999
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<front><div type="abstract" xml:lang="en"><p id="P1">Zoonotic viruses, such as HIV, Ebola virus, coronaviruses, influenza A viruses, hantaviruses, or henipaviruses, can result in profound pathology in humans. In contrast, populations of the reservoir hosts of zoonotic pathogens often appear to tolerate these infections with little evidence of disease. Why are viruses more dangerous in one species than another? Immunological studies investigating quantitative and qualitative differences in the host-virus equilibrium in animal reservoirs will be key to answering this question, informing new approaches for treating and preventing zoonotic diseases. Integrating an understanding of host immune responses with epidemiological, ecological, and evolutionary insights into viral emergence will shed light on mechanisms that minimize fitness costs associated with viral infection, facilitate transmission to other hosts, and underlie the association of specific reservoir hosts with multiple emerging viruses. Reservoir host studies provide a rich opportunity for elucidating fundamental immunological processes and their underlying genetic basis, in the context of distinct physiological and metabolic constraints that contribute to host resistance and disease tolerance.</p>
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<title-group><article-title>Reservoir Host Immune Responses to Emerging Zoonotic Viruses</article-title>
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<contrib-group><contrib contrib-type="author"><name><surname>Mandl</surname>
<given-names>Judith N.</given-names>
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<xref ref-type="aff" rid="A1">1</xref>
<xref rid="FN2" ref-type="author-notes">7</xref>
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Lymphocyte Biology Section, Laboratory of Systems Biology, NIAID, National Institutes of Health, Bethesda, MD 20892, USA</aff>
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Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322, USA</aff>
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Sainte-Justine Hospital Research Centre, Department of Pediatrics, University of Montreal, Montreal, QC H3T 1J4, Canada</aff>
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EcoHealth Alliance, New York, NY 10001, USA</aff>
<aff id="A5"><label>5</label>
Department of Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA</aff>
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Merck Vaccines, Merck & Co. Inc., West Point, PA 19486, USA</aff>
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Correspondence: <email>mandlj@niaid.nih.gov</email>
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<p>Present address: Department of Physiology and Complex Traits Group, McGill University, Montreal, QC H3G 0B1, Canada</p>
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<abstract><p id="P1">Zoonotic viruses, such as HIV, Ebola virus, coronaviruses, influenza A viruses, hantaviruses, or henipaviruses, can result in profound pathology in humans. In contrast, populations of the reservoir hosts of zoonotic pathogens often appear to tolerate these infections with little evidence of disease. Why are viruses more dangerous in one species than another? Immunological studies investigating quantitative and qualitative differences in the host-virus equilibrium in animal reservoirs will be key to answering this question, informing new approaches for treating and preventing zoonotic diseases. Integrating an understanding of host immune responses with epidemiological, ecological, and evolutionary insights into viral emergence will shed light on mechanisms that minimize fitness costs associated with viral infection, facilitate transmission to other hosts, and underlie the association of specific reservoir hosts with multiple emerging viruses. Reservoir host studies provide a rich opportunity for elucidating fundamental immunological processes and their underlying genetic basis, in the context of distinct physiological and metabolic constraints that contribute to host resistance and disease tolerance.</p>
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