Coreceptor Switching in HIV-1 Subtype B and Subtype C

We use a mathematical model to determine the factors affecting the delayed or rare coreceptor switch in HIV-1 subtype C infected individuals. The model takes into account the two main target cells for the CXCR4-tropic and CCR5-tropic virus and includes the the lytic and non-lytic immune responses. C...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Bulletin of mathematical biology 2007, Vol.69 (1), p.55-75
Hauptverfasser: Mugwagwa, T, Witten, G
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 75
container_issue 1
container_start_page 55
container_title Bulletin of mathematical biology
container_volume 69
creator Mugwagwa, T
Witten, G
description We use a mathematical model to determine the factors affecting the delayed or rare coreceptor switch in HIV-1 subtype C infected individuals. The model takes into account the two main target cells for the CXCR4-tropic and CCR5-tropic virus and includes the the lytic and non-lytic immune responses. Computer-based simulations and a sensitivity analysis of the model predict that a persistent immune response suppresses the CXCR4-tropic virus to low levels and hence preventing a phenotypic switch. However, not only should the immune response be persistent, but it should have an efficient lytic immune response rather that an efficient non-lytic response. In addition, we also find that the availability of macrophage cells and enhanced viral kinetics are also crucial for the dominance of the R5 strain. We suggest that an altered host environment probably as a result of immune activation may explain the difference in coreceptor switching kinetics between HIV-1 subtype B and subtype C individuals.
doi_str_mv 10.1007/s11538-006-9137-1
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68933735</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1930795971</sourcerecordid><originalsourceid>FETCH-LOGICAL-c333t-924a8cf7169076e96ea908ba4e356671fe5750410e3b1bf2c165c137edba97a23</originalsourceid><addsrcrecordid>eNqFkEtLxDAUhYMoOj5-gBstLtxF781tkmapgy8QXIy6DWknHSsz7Zi0iP_eDDMouHF1ufCdA-dj7BjhAgH0ZUSUVHAAxQ2S5rjFRiiF4EaB2GYjACN4IXLYY_sxvkPKGDK7bA81FIo0jJgcd8FXftl3IZt8Nn311rSzrGmz-4dXjtlkKPuvpc-uM9dOf77xIdup3Tz6o809YC-3N8_je_74dPcwvnrkFRH13IjcFVWtURnQyhvlnYGidLknqZTG2kstIUfwVGJZiwqVrNIQPy2d0U7QATtf9y5D9zH42NtFEys_n7vWd0O0qjBEmuS_oACSgpRO4Nkf8L0bQptGJCZpg1xQgnANVaGLMfjaLkOzcOHLItiVebs2b5N5uzJvMWVONsVDufDT38RGdQJO10DtOutmoYn2ZSIACVALKISkb5urg44</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>209600423</pqid></control><display><type>article</type><title>Coreceptor Switching in HIV-1 Subtype B and Subtype C</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>Mugwagwa, T ; Witten, G</creator><creatorcontrib>Mugwagwa, T ; Witten, G</creatorcontrib><description>We use a mathematical model to determine the factors affecting the delayed or rare coreceptor switch in HIV-1 subtype C infected individuals. The model takes into account the two main target cells for the CXCR4-tropic and CCR5-tropic virus and includes the the lytic and non-lytic immune responses. Computer-based simulations and a sensitivity analysis of the model predict that a persistent immune response suppresses the CXCR4-tropic virus to low levels and hence preventing a phenotypic switch. However, not only should the immune response be persistent, but it should have an efficient lytic immune response rather that an efficient non-lytic response. In addition, we also find that the availability of macrophage cells and enhanced viral kinetics are also crucial for the dominance of the R5 strain. We suggest that an altered host environment probably as a result of immune activation may explain the difference in coreceptor switching kinetics between HIV-1 subtype B and subtype C individuals.</description><identifier>ISSN: 0092-8240</identifier><identifier>EISSN: 1522-9602</identifier><identifier>DOI: 10.1007/s11538-006-9137-1</identifier><identifier>PMID: 17086370</identifier><language>eng</language><publisher>United States: New York : Springer-Verlag</publisher><subject>HIV Infections - virology ; HIV-1 - classification ; HIV-1 - physiology ; Human immunodeficiency virus 1 ; Humans ; Models, Biological ; Receptors, CCR5 - metabolism ; Receptors, CXCR4 - metabolism</subject><ispartof>Bulletin of mathematical biology, 2007, Vol.69 (1), p.55-75</ispartof><rights>Springer Science+Business Media, Inc. 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c333t-924a8cf7169076e96ea908ba4e356671fe5750410e3b1bf2c165c137edba97a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17086370$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mugwagwa, T</creatorcontrib><creatorcontrib>Witten, G</creatorcontrib><title>Coreceptor Switching in HIV-1 Subtype B and Subtype C</title><title>Bulletin of mathematical biology</title><addtitle>Bull Math Biol</addtitle><description>We use a mathematical model to determine the factors affecting the delayed or rare coreceptor switch in HIV-1 subtype C infected individuals. The model takes into account the two main target cells for the CXCR4-tropic and CCR5-tropic virus and includes the the lytic and non-lytic immune responses. Computer-based simulations and a sensitivity analysis of the model predict that a persistent immune response suppresses the CXCR4-tropic virus to low levels and hence preventing a phenotypic switch. However, not only should the immune response be persistent, but it should have an efficient lytic immune response rather that an efficient non-lytic response. In addition, we also find that the availability of macrophage cells and enhanced viral kinetics are also crucial for the dominance of the R5 strain. We suggest that an altered host environment probably as a result of immune activation may explain the difference in coreceptor switching kinetics between HIV-1 subtype B and subtype C individuals.</description><subject>HIV Infections - virology</subject><subject>HIV-1 - classification</subject><subject>HIV-1 - physiology</subject><subject>Human immunodeficiency virus 1</subject><subject>Humans</subject><subject>Models, Biological</subject><subject>Receptors, CCR5 - metabolism</subject><subject>Receptors, CXCR4 - metabolism</subject><issn>0092-8240</issn><issn>1522-9602</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</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>eNqFkEtLxDAUhYMoOj5-gBstLtxF781tkmapgy8QXIy6DWknHSsz7Zi0iP_eDDMouHF1ufCdA-dj7BjhAgH0ZUSUVHAAxQ2S5rjFRiiF4EaB2GYjACN4IXLYY_sxvkPKGDK7bA81FIo0jJgcd8FXftl3IZt8Nn311rSzrGmz-4dXjtlkKPuvpc-uM9dOf77xIdup3Tz6o809YC-3N8_je_74dPcwvnrkFRH13IjcFVWtURnQyhvlnYGidLknqZTG2kstIUfwVGJZiwqVrNIQPy2d0U7QATtf9y5D9zH42NtFEys_n7vWd0O0qjBEmuS_oACSgpRO4Nkf8L0bQptGJCZpg1xQgnANVaGLMfjaLkOzcOHLItiVebs2b5N5uzJvMWVONsVDufDT38RGdQJO10DtOutmoYn2ZSIACVALKISkb5urg44</recordid><startdate>2007</startdate><enddate>2007</enddate><creator>Mugwagwa, T</creator><creator>Witten, G</creator><general>New York : Springer-Verlag</general><general>Springer Nature B.V</general><scope>FBQ</scope><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>7SS</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>JQ2</scope><scope>K7-</scope><scope>K9.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>M7S</scope><scope>P5Z</scope><scope>P62</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>2007</creationdate><title>Coreceptor Switching in HIV-1 Subtype B and Subtype C</title><author>Mugwagwa, T ; Witten, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c333t-924a8cf7169076e96ea908ba4e356671fe5750410e3b1bf2c165c137edba97a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>HIV Infections - virology</topic><topic>HIV-1 - classification</topic><topic>HIV-1 - physiology</topic><topic>Human immunodeficiency virus 1</topic><topic>Humans</topic><topic>Models, Biological</topic><topic>Receptors, CCR5 - metabolism</topic><topic>Receptors, CXCR4 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mugwagwa, T</creatorcontrib><creatorcontrib>Witten, G</creatorcontrib><collection>AGRIS</collection><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>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Computer Science Collection</collection><collection>Computer Science Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Bulletin of mathematical biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mugwagwa, T</au><au>Witten, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coreceptor Switching in HIV-1 Subtype B and Subtype C</atitle><jtitle>Bulletin of mathematical biology</jtitle><addtitle>Bull Math Biol</addtitle><date>2007</date><risdate>2007</risdate><volume>69</volume><issue>1</issue><spage>55</spage><epage>75</epage><pages>55-75</pages><issn>0092-8240</issn><eissn>1522-9602</eissn><abstract>We use a mathematical model to determine the factors affecting the delayed or rare coreceptor switch in HIV-1 subtype C infected individuals. The model takes into account the two main target cells for the CXCR4-tropic and CCR5-tropic virus and includes the the lytic and non-lytic immune responses. Computer-based simulations and a sensitivity analysis of the model predict that a persistent immune response suppresses the CXCR4-tropic virus to low levels and hence preventing a phenotypic switch. However, not only should the immune response be persistent, but it should have an efficient lytic immune response rather that an efficient non-lytic response. In addition, we also find that the availability of macrophage cells and enhanced viral kinetics are also crucial for the dominance of the R5 strain. We suggest that an altered host environment probably as a result of immune activation may explain the difference in coreceptor switching kinetics between HIV-1 subtype B and subtype C individuals.</abstract><cop>United States</cop><pub>New York : Springer-Verlag</pub><pmid>17086370</pmid><doi>10.1007/s11538-006-9137-1</doi><tpages>21</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0092-8240
ispartof Bulletin of mathematical biology, 2007, Vol.69 (1), p.55-75
issn 0092-8240
1522-9602
language eng
recordid cdi_proquest_miscellaneous_68933735
source MEDLINE; SpringerLink Journals
subjects HIV Infections - virology
HIV-1 - classification
HIV-1 - physiology
Human immunodeficiency virus 1
Humans
Models, Biological
Receptors, CCR5 - metabolism
Receptors, CXCR4 - metabolism
title Coreceptor Switching in HIV-1 Subtype B and Subtype C
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T05%3A04%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Coreceptor%20Switching%20in%20HIV-1%20Subtype%20B%20and%20Subtype%20C&rft.jtitle=Bulletin%20of%20mathematical%20biology&rft.au=Mugwagwa,%20T&rft.date=2007&rft.volume=69&rft.issue=1&rft.spage=55&rft.epage=75&rft.pages=55-75&rft.issn=0092-8240&rft.eissn=1522-9602&rft_id=info:doi/10.1007/s11538-006-9137-1&rft_dat=%3Cproquest_cross%3E1930795971%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=209600423&rft_id=info:pmid/17086370&rfr_iscdi=true