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Angiotensin-converting enzyme 2 protects from lethal avian influenza A H5N1 infections
The potential for avian influenza H5N1 outbreaks has increased in recent years. Thus, it is paramount to develop novel strategies to alleviate death rates. Here we show that avian influenza A H5N1-infected patients exhibit markedly increased serum levels of angiotensin II. High serum levels of angio...
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Published in: | Nature communications 2014-05, Vol.5 (1), p.3594-3594, Article 3594 |
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creator | Zou, Zhen Yan, Yiwu Shu, Yuelong Gao, Rongbao Sun, Yang Li, Xiao Ju, Xiangwu Liang, Zhu Liu, Qiang Zhao, Yan Guo, Feng Bai, Tian Han, Zongsheng Zhu, Jindong Zhou, Huandi Huang, Fengming Li, Chang Lu, Huijun Li, Ning Li, Dangsheng Jin, Ningyi Penninger, Josef M. Jiang, Chengyu |
description | The potential for avian influenza H5N1 outbreaks has increased in recent years. Thus, it is paramount to develop novel strategies to alleviate death rates. Here we show that avian influenza A H5N1-infected patients exhibit markedly increased serum levels of angiotensin II. High serum levels of angiotensin II appear to be linked to the severity and lethality of infection, at least in some patients. In experimental mouse models, infection with highly pathogenic avian influenza A H5N1 virus results in downregulation of angiotensin-converting enzyme 2 (ACE2) expression in the lung and increased serum angiotensin II levels. Genetic inactivation of ACE2 causes severe lung injury in H5N1-challenged mice, confirming a role of ACE2 in H5N1-induced lung pathologies. Administration of recombinant human ACE2 ameliorates avian influenza H5N1 virus-induced lung injury in mice. Our data link H5N1 virus-induced acute lung failure to ACE2 and provide a potential treatment strategy to address future flu pandemics.
H5N1 avian influenza viruses can be highly pathogenic. Here, the authors show that H5N1 infection leads to increased serum levels of angiotensin II in patients and mice, and that administration of angiotensin-converting enzyme 2 ameliorates lung injury in infected mice. |
doi_str_mv | 10.1038/ncomms4594 |
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H5N1 avian influenza viruses can be highly pathogenic. Here, the authors show that H5N1 infection leads to increased serum levels of angiotensin II in patients and mice, and that administration of angiotensin-converting enzyme 2 ameliorates lung injury in infected mice.</description><identifier>ISSN: 2041-1723</identifier><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/ncomms4594</identifier><identifier>PMID: 24800825</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/95 ; 38 ; 631/326/596/1578 ; 64/60 ; 692/308 ; 692/699/1785 ; 82/80 ; Adolescent ; Adult ; Animals ; Avian flu ; Birds ; Child ; Child, Preschool ; Disease Models, Animal ; Down-Regulation ; Enzymes ; Female ; History, Ancient ; Humanities and Social Sciences ; Humans ; Infections ; Influenza A Virus, H1N1 Subtype ; Influenza A Virus, H5N1 Subtype - pathogenicity ; Influenza, Human - blood ; Influenza, Human - prevention & control ; Influenza, Human - virology ; Lung - metabolism ; Lung - pathology ; Lung Injury - drug therapy ; Lung Injury - genetics ; Lungs ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Knockout ; Middle Aged ; Molecular biology ; multidisciplinary ; Orthomyxoviridae Infections - blood ; Orthomyxoviridae Infections - prevention & control ; Orthomyxoviridae Infections - virology ; Peptidyl-Dipeptidase A - biosynthesis ; Peptidyl-Dipeptidase A - blood ; Peptidyl-Dipeptidase A - genetics ; Peptidyl-Dipeptidase A - pharmacology ; Recombinant Proteins - pharmacology ; Science ; Science (multidisciplinary) ; Sepsis ; Viruses ; Young Adult</subject><ispartof>Nature communications, 2014-05, Vol.5 (1), p.3594-3594, Article 3594</ispartof><rights>Springer Nature Limited 2014</rights><rights>Copyright Nature Publishing Group May 2014</rights><rights>Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-22a383edab52e81be135170fc319bf22b0d21ea9722edab59dc19c1c10bbd9393</citedby><cites>FETCH-LOGICAL-c442t-22a383edab52e81be135170fc319bf22b0d21ea9722edab59dc19c1c10bbd9393</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1521028193/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1521028193?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,38516,43895,44590,53791,53793,74412,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24800825$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zou, Zhen</creatorcontrib><creatorcontrib>Yan, Yiwu</creatorcontrib><creatorcontrib>Shu, Yuelong</creatorcontrib><creatorcontrib>Gao, Rongbao</creatorcontrib><creatorcontrib>Sun, Yang</creatorcontrib><creatorcontrib>Li, Xiao</creatorcontrib><creatorcontrib>Ju, Xiangwu</creatorcontrib><creatorcontrib>Liang, Zhu</creatorcontrib><creatorcontrib>Liu, Qiang</creatorcontrib><creatorcontrib>Zhao, Yan</creatorcontrib><creatorcontrib>Guo, Feng</creatorcontrib><creatorcontrib>Bai, Tian</creatorcontrib><creatorcontrib>Han, Zongsheng</creatorcontrib><creatorcontrib>Zhu, Jindong</creatorcontrib><creatorcontrib>Zhou, Huandi</creatorcontrib><creatorcontrib>Huang, Fengming</creatorcontrib><creatorcontrib>Li, Chang</creatorcontrib><creatorcontrib>Lu, Huijun</creatorcontrib><creatorcontrib>Li, Ning</creatorcontrib><creatorcontrib>Li, Dangsheng</creatorcontrib><creatorcontrib>Jin, Ningyi</creatorcontrib><creatorcontrib>Penninger, Josef M.</creatorcontrib><creatorcontrib>Jiang, Chengyu</creatorcontrib><title>Angiotensin-converting enzyme 2 protects from lethal avian influenza A H5N1 infections</title><title>Nature communications</title><addtitle>Nat Commun</addtitle><addtitle>Nat Commun</addtitle><description>The potential for avian influenza H5N1 outbreaks has increased in recent years. Thus, it is paramount to develop novel strategies to alleviate death rates. Here we show that avian influenza A H5N1-infected patients exhibit markedly increased serum levels of angiotensin II. High serum levels of angiotensin II appear to be linked to the severity and lethality of infection, at least in some patients. In experimental mouse models, infection with highly pathogenic avian influenza A H5N1 virus results in downregulation of angiotensin-converting enzyme 2 (ACE2) expression in the lung and increased serum angiotensin II levels. Genetic inactivation of ACE2 causes severe lung injury in H5N1-challenged mice, confirming a role of ACE2 in H5N1-induced lung pathologies. Administration of recombinant human ACE2 ameliorates avian influenza H5N1 virus-induced lung injury in mice. Our data link H5N1 virus-induced acute lung failure to ACE2 and provide a potential treatment strategy to address future flu pandemics.
H5N1 avian influenza viruses can be highly pathogenic. Here, the authors show that H5N1 infection leads to increased serum levels of angiotensin II in patients and mice, and that administration of angiotensin-converting enzyme 2 ameliorates lung injury in infected mice.</description><subject>13/95</subject><subject>38</subject><subject>631/326/596/1578</subject><subject>64/60</subject><subject>692/308</subject><subject>692/699/1785</subject><subject>82/80</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Animals</subject><subject>Avian flu</subject><subject>Birds</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Disease Models, Animal</subject><subject>Down-Regulation</subject><subject>Enzymes</subject><subject>Female</subject><subject>History, Ancient</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Infections</subject><subject>Influenza A Virus, H1N1 Subtype</subject><subject>Influenza A Virus, H5N1 Subtype - 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pharmacology</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Sepsis</subject><subject>Viruses</subject><subject>Young 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Commun</addtitle><date>2014-05-06</date><risdate>2014</risdate><volume>5</volume><issue>1</issue><spage>3594</spage><epage>3594</epage><pages>3594-3594</pages><artnum>3594</artnum><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>The potential for avian influenza H5N1 outbreaks has increased in recent years. Thus, it is paramount to develop novel strategies to alleviate death rates. Here we show that avian influenza A H5N1-infected patients exhibit markedly increased serum levels of angiotensin II. High serum levels of angiotensin II appear to be linked to the severity and lethality of infection, at least in some patients. In experimental mouse models, infection with highly pathogenic avian influenza A H5N1 virus results in downregulation of angiotensin-converting enzyme 2 (ACE2) expression in the lung and increased serum angiotensin II levels. Genetic inactivation of ACE2 causes severe lung injury in H5N1-challenged mice, confirming a role of ACE2 in H5N1-induced lung pathologies. Administration of recombinant human ACE2 ameliorates avian influenza H5N1 virus-induced lung injury in mice. Our data link H5N1 virus-induced acute lung failure to ACE2 and provide a potential treatment strategy to address future flu pandemics.
H5N1 avian influenza viruses can be highly pathogenic. Here, the authors show that H5N1 infection leads to increased serum levels of angiotensin II in patients and mice, and that administration of angiotensin-converting enzyme 2 ameliorates lung injury in infected mice.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>24800825</pmid><doi>10.1038/ncomms4594</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7091848 |
source | Publicly Available Content Database; Nature Journals Online; PubMed Central; Coronavirus Research Database; Springer Nature - nature.com Journals - Fully Open Access |
subjects | 13/95 38 631/326/596/1578 64/60 692/308 692/699/1785 82/80 Adolescent Adult Animals Avian flu Birds Child Child, Preschool Disease Models, Animal Down-Regulation Enzymes Female History, Ancient Humanities and Social Sciences Humans Infections Influenza A Virus, H1N1 Subtype Influenza A Virus, H5N1 Subtype - pathogenicity Influenza, Human - blood Influenza, Human - prevention & control Influenza, Human - virology Lung - metabolism Lung - pathology Lung Injury - drug therapy Lung Injury - genetics Lungs Male Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Knockout Middle Aged Molecular biology multidisciplinary Orthomyxoviridae Infections - blood Orthomyxoviridae Infections - prevention & control Orthomyxoviridae Infections - virology Peptidyl-Dipeptidase A - biosynthesis Peptidyl-Dipeptidase A - blood Peptidyl-Dipeptidase A - genetics Peptidyl-Dipeptidase A - pharmacology Recombinant Proteins - pharmacology Science Science (multidisciplinary) Sepsis Viruses Young Adult |
title | Angiotensin-converting enzyme 2 protects from lethal avian influenza A H5N1 infections |
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