Dengue Virus Serotype-2 Impairs Proliferation of Healthy Donors' T Lymphocytes
Objectives: T lymphocytes are not infected by dengue virus (DENV), nevertheless it is possible that exposure to DENV may affect their function. T lymphocytes from DENV-infected individuals are impaired in their proliferative capacity, although this effect has been attributed to altered function of a...
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Veröffentlicht in: | Intervirology 2014-01, Vol.57 (2), p.83-92 |
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creator | Fuentes-Miranda, C.J. Sánchez-García, F.J. Coker, A.R. Rojas-Espinosa, O. Salinas-Tobón, R. Moreno-Altamirano, M.M.B. |
description | Objectives: T lymphocytes are not infected by dengue virus (DENV), nevertheless it is possible that exposure to DENV may affect their function. T lymphocytes from DENV-infected individuals are impaired in their proliferative capacity, although this effect has been attributed to altered function of antigen-presenting cells rather than to an intrinsic defect on T lymphocytes. Here we analyzed whether T lymphocytes from healthy donors became impaired in their proliferative capacity following in vitro exposure to DENV serotype-2 (DENV-2), as well as the possible mechanisms for this. Methods: Isolated CD4+ and CD8+ T lymphocytes from healthy donors were in vitro exposed to DENV-2, before polyclonal activation, cell proliferation, IL-2 synthesis. IL-2Rα expression, nuclear translocation of NF-AT and NF-κB, and intracellular calcium flux were assessed. Results: In vitro exposure of both CD4+ and CD8+ T lymphocytes from healthy donors to DENV-2 impairs cell proliferation, IL-2 synthesis, and IL-2Rα (CD25) cell membrane expression. Signalling wise, exposure to DENV-2 impairs the nuclear translocation of NF-AT, downstream of intracellular calcium mobilization, as well as that of NF-κB. Conclusion: In the course of a dengue infection, direct exposure of T lymphocytes to DENV could affect cell-mediated immune responses. |
doi_str_mv | 10.1159/000357180 |
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T lymphocytes from DENV-infected individuals are impaired in their proliferative capacity, although this effect has been attributed to altered function of antigen-presenting cells rather than to an intrinsic defect on T lymphocytes. Here we analyzed whether T lymphocytes from healthy donors became impaired in their proliferative capacity following in vitro exposure to DENV serotype-2 (DENV-2), as well as the possible mechanisms for this. Methods: Isolated CD4+ and CD8+ T lymphocytes from healthy donors were in vitro exposed to DENV-2, before polyclonal activation, cell proliferation, IL-2 synthesis. IL-2Rα expression, nuclear translocation of NF-AT and NF-κB, and intracellular calcium flux were assessed. Results: In vitro exposure of both CD4+ and CD8+ T lymphocytes from healthy donors to DENV-2 impairs cell proliferation, IL-2 synthesis, and IL-2Rα (CD25) cell membrane expression. Signalling wise, exposure to DENV-2 impairs the nuclear translocation of NF-AT, downstream of intracellular calcium mobilization, as well as that of NF-κB. Conclusion: In the course of a dengue infection, direct exposure of T lymphocytes to DENV could affect cell-mediated immune responses.</description><identifier>ISSN: 0300-5526</identifier><identifier>EISSN: 1423-0100</identifier><identifier>DOI: 10.1159/000357180</identifier><identifier>PMID: 24480857</identifier><identifier>CODEN: IVRYAK</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Cell Proliferation ; Cells, Cultured ; Dengue virus ; Dengue Virus - immunology ; Host-Pathogen Interactions ; Humans ; Immune Evasion ; Interleukin-2 - secretion ; NF-kappa B - metabolism ; NFATC Transcription Factors - metabolism ; Original Paper ; Receptors, Interleukin-2 - biosynthesis ; T-Lymphocytes - immunology ; T-Lymphocytes - virology</subject><ispartof>Intervirology, 2014-01, Vol.57 (2), p.83-92</ispartof><rights>2014 S. Karger AG, Basel</rights><rights>Copyright (c) 2014 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-378e785241bd5584a4b05eceda54a3560a91fcca94f9df63d3df0af7be4320103</citedby><cites>FETCH-LOGICAL-c402t-378e785241bd5584a4b05eceda54a3560a91fcca94f9df63d3df0af7be4320103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2429,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24480857$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fuentes-Miranda, C.J.</creatorcontrib><creatorcontrib>Sánchez-García, F.J.</creatorcontrib><creatorcontrib>Coker, A.R.</creatorcontrib><creatorcontrib>Rojas-Espinosa, O.</creatorcontrib><creatorcontrib>Salinas-Tobón, R.</creatorcontrib><creatorcontrib>Moreno-Altamirano, M.M.B.</creatorcontrib><title>Dengue Virus Serotype-2 Impairs Proliferation of Healthy Donors' T Lymphocytes</title><title>Intervirology</title><addtitle>Intervirology</addtitle><description>Objectives: T lymphocytes are not infected by dengue virus (DENV), nevertheless it is possible that exposure to DENV may affect their function. T lymphocytes from DENV-infected individuals are impaired in their proliferative capacity, although this effect has been attributed to altered function of antigen-presenting cells rather than to an intrinsic defect on T lymphocytes. Here we analyzed whether T lymphocytes from healthy donors became impaired in their proliferative capacity following in vitro exposure to DENV serotype-2 (DENV-2), as well as the possible mechanisms for this. Methods: Isolated CD4+ and CD8+ T lymphocytes from healthy donors were in vitro exposed to DENV-2, before polyclonal activation, cell proliferation, IL-2 synthesis. IL-2Rα expression, nuclear translocation of NF-AT and NF-κB, and intracellular calcium flux were assessed. Results: In vitro exposure of both CD4+ and CD8+ T lymphocytes from healthy donors to DENV-2 impairs cell proliferation, IL-2 synthesis, and IL-2Rα (CD25) cell membrane expression. Signalling wise, exposure to DENV-2 impairs the nuclear translocation of NF-AT, downstream of intracellular calcium mobilization, as well as that of NF-κB. Conclusion: In the course of a dengue infection, direct exposure of T lymphocytes to DENV could affect cell-mediated immune responses.</description><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>Dengue virus</subject><subject>Dengue Virus - immunology</subject><subject>Host-Pathogen Interactions</subject><subject>Humans</subject><subject>Immune Evasion</subject><subject>Interleukin-2 - secretion</subject><subject>NF-kappa B - metabolism</subject><subject>NFATC Transcription Factors - metabolism</subject><subject>Original Paper</subject><subject>Receptors, Interleukin-2 - biosynthesis</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - virology</subject><issn>0300-5526</issn><issn>1423-0100</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqN0TtLxEAUBeBBFF0fhb3IgIVaRO-8kkkpvmFRwUcbZpM7Gk0ycSYp8u_NsusWVla3-e6BwyFkn8EZYyo9BwChEqZhjUyY5CICBrBOJiAAIqV4vEW2Q_icMyZgk2xxKTVolUzIwxU27z3St9L3gT6jd93QYsTpfd2a0gf65F1VWvSmK11DnaV3aKruY6BXrnE-HNMXOh3q9sPlQ4dhl2xYUwXcW94d8npz_XJ5F00fb-8vL6ZRLoF3kUg0JlpxyWaFUloaOQOFORZGSSNUDCZlNs9NKm1a2FgUorBgbDJDKfhYTuyQk0Vu6913j6HL6jLkWFWmQdeHjCkWJyqOQf6Hcs611PFIj_7QT9f7ZiwyVwmwlKV6VKcLlXsXgkebtb6sjR8yBtl8j2y1x2gPl4n9rMZiJX8HGMHBAnwZ_45-BZb_P5_ri7Q</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Fuentes-Miranda, C.J.</creator><creator>Sánchez-García, F.J.</creator><creator>Coker, A.R.</creator><creator>Rojas-Espinosa, O.</creator><creator>Salinas-Tobón, R.</creator><creator>Moreno-Altamirano, M.M.B.</creator><general>S. Karger AG</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>S0X</scope><scope>7X8</scope><scope>7T2</scope><scope>7T5</scope><scope>7U2</scope><scope>C1K</scope><scope>F1W</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope></search><sort><creationdate>20140101</creationdate><title>Dengue Virus Serotype-2 Impairs Proliferation of Healthy Donors' T Lymphocytes</title><author>Fuentes-Miranda, C.J. ; Sánchez-García, F.J. ; Coker, A.R. ; Rojas-Espinosa, O. ; Salinas-Tobón, R. ; Moreno-Altamirano, M.M.B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-378e785241bd5584a4b05eceda54a3560a91fcca94f9df63d3df0af7be4320103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Dengue virus</topic><topic>Dengue Virus - immunology</topic><topic>Host-Pathogen Interactions</topic><topic>Humans</topic><topic>Immune Evasion</topic><topic>Interleukin-2 - secretion</topic><topic>NF-kappa B - metabolism</topic><topic>NFATC Transcription Factors - metabolism</topic><topic>Original Paper</topic><topic>Receptors, Interleukin-2 - biosynthesis</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes - virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fuentes-Miranda, C.J.</creatorcontrib><creatorcontrib>Sánchez-García, F.J.</creatorcontrib><creatorcontrib>Coker, A.R.</creatorcontrib><creatorcontrib>Rojas-Espinosa, O.</creatorcontrib><creatorcontrib>Salinas-Tobón, R.</creatorcontrib><creatorcontrib>Moreno-Altamirano, M.M.B.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Safety Science and Risk</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Intervirology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fuentes-Miranda, C.J.</au><au>Sánchez-García, F.J.</au><au>Coker, A.R.</au><au>Rojas-Espinosa, O.</au><au>Salinas-Tobón, R.</au><au>Moreno-Altamirano, M.M.B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dengue Virus Serotype-2 Impairs Proliferation of Healthy Donors' T Lymphocytes</atitle><jtitle>Intervirology</jtitle><addtitle>Intervirology</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>57</volume><issue>2</issue><spage>83</spage><epage>92</epage><pages>83-92</pages><issn>0300-5526</issn><eissn>1423-0100</eissn><coden>IVRYAK</coden><abstract>Objectives: T lymphocytes are not infected by dengue virus (DENV), nevertheless it is possible that exposure to DENV may affect their function. T lymphocytes from DENV-infected individuals are impaired in their proliferative capacity, although this effect has been attributed to altered function of antigen-presenting cells rather than to an intrinsic defect on T lymphocytes. Here we analyzed whether T lymphocytes from healthy donors became impaired in their proliferative capacity following in vitro exposure to DENV serotype-2 (DENV-2), as well as the possible mechanisms for this. Methods: Isolated CD4+ and CD8+ T lymphocytes from healthy donors were in vitro exposed to DENV-2, before polyclonal activation, cell proliferation, IL-2 synthesis. IL-2Rα expression, nuclear translocation of NF-AT and NF-κB, and intracellular calcium flux were assessed. Results: In vitro exposure of both CD4+ and CD8+ T lymphocytes from healthy donors to DENV-2 impairs cell proliferation, IL-2 synthesis, and IL-2Rα (CD25) cell membrane expression. Signalling wise, exposure to DENV-2 impairs the nuclear translocation of NF-AT, downstream of intracellular calcium mobilization, as well as that of NF-κB. Conclusion: In the course of a dengue infection, direct exposure of T lymphocytes to DENV could affect cell-mediated immune responses.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>24480857</pmid><doi>10.1159/000357180</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cell Proliferation Cells, Cultured Dengue virus Dengue Virus - immunology Host-Pathogen Interactions Humans Immune Evasion Interleukin-2 - secretion NF-kappa B - metabolism NFATC Transcription Factors - metabolism Original Paper Receptors, Interleukin-2 - biosynthesis T-Lymphocytes - immunology T-Lymphocytes - virology |
title | Dengue Virus Serotype-2 Impairs Proliferation of Healthy Donors' T Lymphocytes |
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