Monocyte heterogeneity underlying phenotypic changes in monocytes according to SIV disease stage
Expansion of two monocyte subpopulations expressing CD16 and their correlation with viral load are observed in this cross‐sectional study of SIV‐infected macaques. Infection by HIV is associated with the expansion of monocytes expressing CD16 antigens, but the significance of this in HIV pathogenesi...
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Veröffentlicht in: | Journal of leukocyte biology 2010-04, Vol.87 (4), p.557-567 |
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creator | Woong-Ki Kim Yue Sun Hien Do Patrick Autissier Elkan F. Halpern Michael Piatak, Jr Jeffrey D. Lifson Tricia H. Burdo Michael S. McGrath Kenneth Williams |
description | Expansion of two monocyte subpopulations expressing CD16 and their correlation with viral load are observed in this cross‐sectional study of SIV‐infected macaques.
Infection by HIV is associated with the expansion of monocytes expressing CD16 antigens, but the significance of this in HIV pathogenesis is largely unknown. In rhesus macaques, at least three subpopulations of blood monocytes were identified based on their expression of CD14 and CD16: CD14highCD16−, CD14highCD16low, and CD14lowCD16high. The phenotypes and functions of these subpopulations, including CD16+ monocytes, were investigated in normal, uninfected rhesus macaques and macaques that were infected with SIV or chimeric SHIV. To assess whether these different monocyte subpopulations expand or contract in AIDS pathogenesis, we conducted a cross‐sectional study of 54 SIV‐ or SHIV‐infected macaques and 48 uninfected controls. The absolute numbers of monocyte populations were examined in acutely infected animals, chronically infected animals with no detectable plasma virus RNA, chronically infected animals with detectable plasma virus RNA, and animals that died with AIDS. The absolute numbers of CD14highCD16low and CD14lowCD16high monocytes were elevated significantly in acutely infected animals and chronically infected animals with detectable plasma virus RNA compared with uninfected controls. Moreover, a significant, positive correlation was evident between the number of CD14highCD16low or CD14lowCD16high monocytes and plasma viral load in the infected cohort. These data show the dynamic changes of blood monocytes, most notably, CD14highCD16low monocytes during lentiviral infection, which are specific to disease stage. |
doi_str_mv | 10.1189/jlb.0209082 |
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Infection by HIV is associated with the expansion of monocytes expressing CD16 antigens, but the significance of this in HIV pathogenesis is largely unknown. In rhesus macaques, at least three subpopulations of blood monocytes were identified based on their expression of CD14 and CD16: CD14highCD16−, CD14highCD16low, and CD14lowCD16high. The phenotypes and functions of these subpopulations, including CD16+ monocytes, were investigated in normal, uninfected rhesus macaques and macaques that were infected with SIV or chimeric SHIV. To assess whether these different monocyte subpopulations expand or contract in AIDS pathogenesis, we conducted a cross‐sectional study of 54 SIV‐ or SHIV‐infected macaques and 48 uninfected controls. The absolute numbers of monocyte populations were examined in acutely infected animals, chronically infected animals with no detectable plasma virus RNA, chronically infected animals with detectable plasma virus RNA, and animals that died with AIDS. The absolute numbers of CD14highCD16low and CD14lowCD16high monocytes were elevated significantly in acutely infected animals and chronically infected animals with detectable plasma virus RNA compared with uninfected controls. Moreover, a significant, positive correlation was evident between the number of CD14highCD16low or CD14lowCD16high monocytes and plasma viral load in the infected cohort. These data show the dynamic changes of blood monocytes, most notably, CD14highCD16low monocytes during lentiviral infection, which are specific to disease stage.</description><identifier>ISSN: 0741-5400</identifier><identifier>EISSN: 1938-3673</identifier><identifier>DOI: 10.1189/jlb.0209082</identifier><identifier>PMID: 19843579</identifier><language>eng</language><publisher>United States: Society for Leukocyte Biology</publisher><subject>Acquired Immunodeficiency Syndrome - blood ; Acquired Immunodeficiency Syndrome - genetics ; Acquired Immunodeficiency Syndrome - immunology ; AIDS ; Animals ; CD16 ; Chimera - genetics ; Chimera - immunology ; Gene Expression Regulation - immunology ; HIV ; HIV-1 - genetics ; HIV-1 - immunology ; Leukocyte Count ; Lipopolysaccharide Receptors - blood ; Lipopolysaccharide Receptors - genetics ; Lipopolysaccharide Receptors - immunology ; Macaca mulatta ; macrophage ; Monocytes - immunology ; Monocytes - metabolism ; Monocytes - virology ; Receptors, IgG - biosynthesis ; Receptors, IgG - genetics ; Receptors, IgG - immunology ; RNA, Viral - blood ; Simian Acquired Immunodeficiency Syndrome - blood ; Simian Acquired Immunodeficiency Syndrome - genetics ; Simian Acquired Immunodeficiency Syndrome - immunology ; Simian Immunodeficiency Virus - genetics ; Simian Immunodeficiency Virus - immunology ; Simian Immunodeficiency Virus - metabolism ; Spotlight on Leading Edge Research ; subsets ; Viral Load - immunology</subject><ispartof>Journal of leukocyte biology, 2010-04, Vol.87 (4), p.557-567</ispartof><rights>2010 Society for Leukocyte Biology</rights><rights>2010 Society for Leukocyte Biology 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5177-18f282e6227222f99a5af5f5a3bd51dc74286e78ecda89469b49e0220c9dc82c3</citedby><cites>FETCH-LOGICAL-c5177-18f282e6227222f99a5af5f5a3bd51dc74286e78ecda89469b49e0220c9dc82c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1189%2Fjlb.0209082$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1189%2Fjlb.0209082$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19843579$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Woong-Ki Kim</creatorcontrib><creatorcontrib>Yue Sun</creatorcontrib><creatorcontrib>Hien Do</creatorcontrib><creatorcontrib>Patrick Autissier</creatorcontrib><creatorcontrib>Elkan F. Halpern</creatorcontrib><creatorcontrib>Michael Piatak, Jr</creatorcontrib><creatorcontrib>Jeffrey D. Lifson</creatorcontrib><creatorcontrib>Tricia H. Burdo</creatorcontrib><creatorcontrib>Michael S. McGrath</creatorcontrib><creatorcontrib>Kenneth Williams</creatorcontrib><title>Monocyte heterogeneity underlying phenotypic changes in monocytes according to SIV disease stage</title><title>Journal of leukocyte biology</title><addtitle>J Leukoc Biol</addtitle><description>Expansion of two monocyte subpopulations expressing CD16 and their correlation with viral load are observed in this cross‐sectional study of SIV‐infected macaques.
Infection by HIV is associated with the expansion of monocytes expressing CD16 antigens, but the significance of this in HIV pathogenesis is largely unknown. In rhesus macaques, at least three subpopulations of blood monocytes were identified based on their expression of CD14 and CD16: CD14highCD16−, CD14highCD16low, and CD14lowCD16high. The phenotypes and functions of these subpopulations, including CD16+ monocytes, were investigated in normal, uninfected rhesus macaques and macaques that were infected with SIV or chimeric SHIV. To assess whether these different monocyte subpopulations expand or contract in AIDS pathogenesis, we conducted a cross‐sectional study of 54 SIV‐ or SHIV‐infected macaques and 48 uninfected controls. The absolute numbers of monocyte populations were examined in acutely infected animals, chronically infected animals with no detectable plasma virus RNA, chronically infected animals with detectable plasma virus RNA, and animals that died with AIDS. The absolute numbers of CD14highCD16low and CD14lowCD16high monocytes were elevated significantly in acutely infected animals and chronically infected animals with detectable plasma virus RNA compared with uninfected controls. Moreover, a significant, positive correlation was evident between the number of CD14highCD16low or CD14lowCD16high monocytes and plasma viral load in the infected cohort. These data show the dynamic changes of blood monocytes, most notably, CD14highCD16low monocytes during lentiviral infection, which are specific to disease stage.</description><subject>Acquired Immunodeficiency Syndrome - blood</subject><subject>Acquired Immunodeficiency Syndrome - genetics</subject><subject>Acquired Immunodeficiency Syndrome - immunology</subject><subject>AIDS</subject><subject>Animals</subject><subject>CD16</subject><subject>Chimera - genetics</subject><subject>Chimera - immunology</subject><subject>Gene Expression Regulation - immunology</subject><subject>HIV</subject><subject>HIV-1 - genetics</subject><subject>HIV-1 - immunology</subject><subject>Leukocyte Count</subject><subject>Lipopolysaccharide Receptors - blood</subject><subject>Lipopolysaccharide Receptors - genetics</subject><subject>Lipopolysaccharide Receptors - immunology</subject><subject>Macaca mulatta</subject><subject>macrophage</subject><subject>Monocytes - immunology</subject><subject>Monocytes - metabolism</subject><subject>Monocytes - virology</subject><subject>Receptors, IgG - biosynthesis</subject><subject>Receptors, IgG - genetics</subject><subject>Receptors, IgG - immunology</subject><subject>RNA, Viral - blood</subject><subject>Simian Acquired Immunodeficiency Syndrome - blood</subject><subject>Simian Acquired Immunodeficiency Syndrome - genetics</subject><subject>Simian Acquired Immunodeficiency Syndrome - immunology</subject><subject>Simian Immunodeficiency Virus - genetics</subject><subject>Simian Immunodeficiency Virus - immunology</subject><subject>Simian Immunodeficiency Virus - metabolism</subject><subject>Spotlight on Leading Edge Research</subject><subject>subsets</subject><subject>Viral Load - immunology</subject><issn>0741-5400</issn><issn>1938-3673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtv1DAUhS0EokNhxR55g1igFD_i2N4gQcWj1SAWPLbG49wkrhJ7sDON8u_JaKICm67u4n7nnKt7EHpOyQWlSr-56XcXhBFNFHuANlRzVfBK8odoQ2RJC1EScoae5HxDCOGsIo_RGdWq5ELqDfr1JYbo5hFwByOk2EIAP874EGpI_exDi_cdhDjOe--w62xoIWMf8LDqMrbOxVQfyTHib1c_ce0z2Aw4j7aFp-hRY_sMz9Z5jn58_PD98nOx_frp6vLdtnCCSllQ1TDFoGJMMsYara2wjWiE5bta0NrJkqkKpAJXW6XLSu9KDYQx4nTtFHP8HL09-e4PuwFqB2FMtjf75AebZhOtN_9vgu9MG28NU0JxQheDV6tBir8PkEcz-Oyg722AeMhGcr48TUqxkK9PpEsx5wTNXQol5liJWSoxayUL_eLfw_6yawcLQE7A5HuY7_My19v3RAi5SF6eJJ1vu8knMHmwfb8kMDNNk5KmNEfuD4yrpc4</recordid><startdate>201004</startdate><enddate>201004</enddate><creator>Woong-Ki Kim</creator><creator>Yue Sun</creator><creator>Hien Do</creator><creator>Patrick Autissier</creator><creator>Elkan F. Halpern</creator><creator>Michael Piatak, Jr</creator><creator>Jeffrey D. Lifson</creator><creator>Tricia H. Burdo</creator><creator>Michael S. McGrath</creator><creator>Kenneth Williams</creator><general>Society for Leukocyte Biology</general><general>The Society for Leukocyte Biology</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>201004</creationdate><title>Monocyte heterogeneity underlying phenotypic changes in monocytes according to SIV disease stage</title><author>Woong-Ki Kim ; Yue Sun ; Hien Do ; Patrick Autissier ; Elkan F. Halpern ; Michael Piatak, Jr ; Jeffrey D. Lifson ; Tricia H. Burdo ; Michael S. 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Halpern</creatorcontrib><creatorcontrib>Michael Piatak, Jr</creatorcontrib><creatorcontrib>Jeffrey D. Lifson</creatorcontrib><creatorcontrib>Tricia H. Burdo</creatorcontrib><creatorcontrib>Michael S. McGrath</creatorcontrib><creatorcontrib>Kenneth Williams</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of leukocyte biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Woong-Ki Kim</au><au>Yue Sun</au><au>Hien Do</au><au>Patrick Autissier</au><au>Elkan F. Halpern</au><au>Michael Piatak, Jr</au><au>Jeffrey D. Lifson</au><au>Tricia H. Burdo</au><au>Michael S. McGrath</au><au>Kenneth Williams</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monocyte heterogeneity underlying phenotypic changes in monocytes according to SIV disease stage</atitle><jtitle>Journal of leukocyte biology</jtitle><addtitle>J Leukoc Biol</addtitle><date>2010-04</date><risdate>2010</risdate><volume>87</volume><issue>4</issue><spage>557</spage><epage>567</epage><pages>557-567</pages><issn>0741-5400</issn><eissn>1938-3673</eissn><abstract>Expansion of two monocyte subpopulations expressing CD16 and their correlation with viral load are observed in this cross‐sectional study of SIV‐infected macaques.
Infection by HIV is associated with the expansion of monocytes expressing CD16 antigens, but the significance of this in HIV pathogenesis is largely unknown. In rhesus macaques, at least three subpopulations of blood monocytes were identified based on their expression of CD14 and CD16: CD14highCD16−, CD14highCD16low, and CD14lowCD16high. The phenotypes and functions of these subpopulations, including CD16+ monocytes, were investigated in normal, uninfected rhesus macaques and macaques that were infected with SIV or chimeric SHIV. To assess whether these different monocyte subpopulations expand or contract in AIDS pathogenesis, we conducted a cross‐sectional study of 54 SIV‐ or SHIV‐infected macaques and 48 uninfected controls. The absolute numbers of monocyte populations were examined in acutely infected animals, chronically infected animals with no detectable plasma virus RNA, chronically infected animals with detectable plasma virus RNA, and animals that died with AIDS. The absolute numbers of CD14highCD16low and CD14lowCD16high monocytes were elevated significantly in acutely infected animals and chronically infected animals with detectable plasma virus RNA compared with uninfected controls. Moreover, a significant, positive correlation was evident between the number of CD14highCD16low or CD14lowCD16high monocytes and plasma viral load in the infected cohort. These data show the dynamic changes of blood monocytes, most notably, CD14highCD16low monocytes during lentiviral infection, which are specific to disease stage.</abstract><cop>United States</cop><pub>Society for Leukocyte Biology</pub><pmid>19843579</pmid><doi>10.1189/jlb.0209082</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acquired Immunodeficiency Syndrome - blood Acquired Immunodeficiency Syndrome - genetics Acquired Immunodeficiency Syndrome - immunology AIDS Animals CD16 Chimera - genetics Chimera - immunology Gene Expression Regulation - immunology HIV HIV-1 - genetics HIV-1 - immunology Leukocyte Count Lipopolysaccharide Receptors - blood Lipopolysaccharide Receptors - genetics Lipopolysaccharide Receptors - immunology Macaca mulatta macrophage Monocytes - immunology Monocytes - metabolism Monocytes - virology Receptors, IgG - biosynthesis Receptors, IgG - genetics Receptors, IgG - immunology RNA, Viral - blood Simian Acquired Immunodeficiency Syndrome - blood Simian Acquired Immunodeficiency Syndrome - genetics Simian Acquired Immunodeficiency Syndrome - immunology Simian Immunodeficiency Virus - genetics Simian Immunodeficiency Virus - immunology Simian Immunodeficiency Virus - metabolism Spotlight on Leading Edge Research subsets Viral Load - immunology |
title | Monocyte heterogeneity underlying phenotypic changes in monocytes according to SIV disease stage |
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