Longitudinal study of HIV-specific cytotoxic lymphocytes in HIV type 1-infected patients : Relative balance between host immune response and the spread of HIV type 1 infection
To evaluate the contribution of a specific cytotoxic response in the control of HIV infection in relation to clinical status, we performed serial analysis of anti-Env and anti-Gag cytotoxic activity in 13 infected individuals over a 6- to 10-year period, using cryopreserved peripheral blood mononucl...
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Veröffentlicht in: | AIDS research and human retroviruses 1997-10, Vol.13 (15), p.1301-1312 |
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description | To evaluate the contribution of a specific cytotoxic response in the control of HIV infection in relation to clinical status, we performed serial analysis of anti-Env and anti-Gag cytotoxic activity in 13 infected individuals over a 6- to 10-year period, using cryopreserved peripheral blood mononuclear cells (PBMCs). Autologous EBV-transformed B cell lines infected in vitro with recombinant vaccinia viruses expressing HIV-1 env and gag genes were used as targets. Without any stimulation of the effector cells, we were able to show an anti-HIV cytotoxic activity in the PBMCs of 12 of 13 HIV-1-infected patients, consistent with chronic immune activation in HIV infection. Different patterns of HIV-specific cytotoxic activity were observed, and the extent of this cytotoxic response varied between the clinically defined groups of individuals. No direct relationship was observed with the number of CD4 and CD8 lymphocytes during the observation period. However, patients who remained asymptomatic had a more vigorous cytotoxic response than patients with clinical deterioration during the observation period, and a significant difference was observed for HIV Gag-specific CTL activity. From these data, we suggest that the HIV-specific cytotoxic response has a protective role in the course of HIV infection. |
doi_str_mv | 10.1089/aid.1997.13.1301 |
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Autologous EBV-transformed B cell lines infected in vitro with recombinant vaccinia viruses expressing HIV-1 env and gag genes were used as targets. Without any stimulation of the effector cells, we were able to show an anti-HIV cytotoxic activity in the PBMCs of 12 of 13 HIV-1-infected patients, consistent with chronic immune activation in HIV infection. Different patterns of HIV-specific cytotoxic activity were observed, and the extent of this cytotoxic response varied between the clinically defined groups of individuals. No direct relationship was observed with the number of CD4 and CD8 lymphocytes during the observation period. However, patients who remained asymptomatic had a more vigorous cytotoxic response than patients with clinical deterioration during the observation period, and a significant difference was observed for HIV Gag-specific CTL activity. From these data, we suggest that the HIV-specific cytotoxic response has a protective role in the course of HIV infection.</description><identifier>ISSN: 0889-2229</identifier><identifier>EISSN: 1931-8405</identifier><identifier>DOI: 10.1089/aid.1997.13.1301</identifier><identifier>PMID: 9339847</identifier><identifier>CODEN: ARHRE7</identifier><language>eng</language><publisher>Larchmont, NY: Liebert</publisher><subject>B-Lymphocytes - immunology ; Biological and medical sciences ; CD4 Lymphocyte Count ; CD4-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - immunology ; Cryopreservation ; Cytotoxicity Tests, Immunologic ; Gene Expression ; Gene Products, env - genetics ; Gene Products, env - immunology ; HIV Antigens - immunology ; HIV Core Protein p24 - genetics ; HIV Core Protein p24 - immunology ; HIV Infections - diagnosis ; HIV Infections - immunology ; HIV-1 - immunology ; HIV-1 - pathogenicity ; Host-Parasite Interactions ; Human immunodeficiency virus 1 ; Humans ; Immunodeficiencies ; Immunodeficiencies. Immunoglobulinopathies ; Immunopathology ; Leukocytes, Mononuclear - immunology ; Longitudinal Studies ; Lymphocyte Count ; Medical sciences ; Recombination, Genetic ; Survivors ; T-Lymphocytes, Cytotoxic - immunology ; Transformation, Genetic ; Vaccinia virus - genetics ; Viral Load</subject><ispartof>AIDS research and human retroviruses, 1997-10, Vol.13 (15), p.1301-1312</ispartof><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c354t-b568c4d4618abc11f9baaa940e5f5258a1f6d7a74457d6610d275a5318c53b743</citedby><cites>FETCH-LOGICAL-c354t-b568c4d4618abc11f9baaa940e5f5258a1f6d7a74457d6610d275a5318c53b743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,3031,27907,27908</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2854643$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9339847$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BARIOU, C</creatorcontrib><creatorcontrib>GENETET, N</creatorcontrib><creatorcontrib>RUFFAULT, A</creatorcontrib><creatorcontrib>MICHELET, C</creatorcontrib><creatorcontrib>CARTIER, F</creatorcontrib><creatorcontrib>GENETET, B</creatorcontrib><title>Longitudinal study of HIV-specific cytotoxic lymphocytes in HIV type 1-infected patients : Relative balance between host immune response and the spread of HIV type 1 infection</title><title>AIDS research and human retroviruses</title><addtitle>AIDS Res Hum Retroviruses</addtitle><description>To evaluate the contribution of a specific cytotoxic response in the control of HIV infection in relation to clinical status, we performed serial analysis of anti-Env and anti-Gag cytotoxic activity in 13 infected individuals over a 6- to 10-year period, using cryopreserved peripheral blood mononuclear cells (PBMCs). Autologous EBV-transformed B cell lines infected in vitro with recombinant vaccinia viruses expressing HIV-1 env and gag genes were used as targets. Without any stimulation of the effector cells, we were able to show an anti-HIV cytotoxic activity in the PBMCs of 12 of 13 HIV-1-infected patients, consistent with chronic immune activation in HIV infection. Different patterns of HIV-specific cytotoxic activity were observed, and the extent of this cytotoxic response varied between the clinically defined groups of individuals. No direct relationship was observed with the number of CD4 and CD8 lymphocytes during the observation period. However, patients who remained asymptomatic had a more vigorous cytotoxic response than patients with clinical deterioration during the observation period, and a significant difference was observed for HIV Gag-specific CTL activity. From these data, we suggest that the HIV-specific cytotoxic response has a protective role in the course of HIV infection.</description><subject>B-Lymphocytes - immunology</subject><subject>Biological and medical sciences</subject><subject>CD4 Lymphocyte Count</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Cryopreservation</subject><subject>Cytotoxicity Tests, Immunologic</subject><subject>Gene Expression</subject><subject>Gene Products, env - genetics</subject><subject>Gene Products, env - immunology</subject><subject>HIV Antigens - immunology</subject><subject>HIV Core Protein p24 - genetics</subject><subject>HIV Core Protein p24 - immunology</subject><subject>HIV Infections - diagnosis</subject><subject>HIV Infections - immunology</subject><subject>HIV-1 - immunology</subject><subject>HIV-1 - pathogenicity</subject><subject>Host-Parasite Interactions</subject><subject>Human immunodeficiency virus 1</subject><subject>Humans</subject><subject>Immunodeficiencies</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunopathology</subject><subject>Leukocytes, Mononuclear - immunology</subject><subject>Longitudinal Studies</subject><subject>Lymphocyte Count</subject><subject>Medical sciences</subject><subject>Recombination, Genetic</subject><subject>Survivors</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><subject>Transformation, Genetic</subject><subject>Vaccinia virus - genetics</subject><subject>Viral Load</subject><issn>0889-2229</issn><issn>1931-8405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kUGL1TAQx4Mo69vVuxchB_HWZ9IkbeJNFnUXHiyIeg1pMvVF2qQ2qdpP5Vc05ZWFgZlh_vMnmR9Cryg5UiLVO-PdkSrVHikrQegTdKCK0UpyIp6iA5FSVXVdq-foOqWfhBBV1-IKXSnGlOTtAf07xfDD58X5YAacSrHi2OO7--9VmsD63lts1xxz_FuqYR2ncyw9JOzDpsJ5nQDTyocebAaHJ5M9hJzwe_wFhtL8BtyZwQRbMuQ_AAGfY8rYj-MSAM-QphgSYBMczmfAaZrBuP0Ruz2-2PsYXqBnvRkSvNzzDfr26ePX27vq9PD5_vbDqbJM8Fx1opGWO95QaTpLaa86Y4ziBEQvaiEN7RvXmpZz0bqmocTVrTCCUWkF61rObtDbi-80x18LpKxHnywM5SMQl6RpW3NO5SYkF6GdY0oz9Hqa_WjmVVOiN0a6MNIbI02Z3hiVlde799KN4B4Xdihl_mafm2TN0M_leD49ymopeMMZ-w-2apw8</recordid><startdate>19971010</startdate><enddate>19971010</enddate><creator>BARIOU, C</creator><creator>GENETET, N</creator><creator>RUFFAULT, A</creator><creator>MICHELET, C</creator><creator>CARTIER, F</creator><creator>GENETET, B</creator><general>Liebert</general><scope>IQODW</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>7T5</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>19971010</creationdate><title>Longitudinal study of HIV-specific cytotoxic lymphocytes in HIV type 1-infected patients : Relative balance between host immune response and the spread of HIV type 1 infection</title><author>BARIOU, C ; GENETET, N ; RUFFAULT, A ; MICHELET, C ; CARTIER, F ; GENETET, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-b568c4d4618abc11f9baaa940e5f5258a1f6d7a74457d6610d275a5318c53b743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>B-Lymphocytes - immunology</topic><topic>Biological and medical sciences</topic><topic>CD4 Lymphocyte Count</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>Cryopreservation</topic><topic>Cytotoxicity Tests, Immunologic</topic><topic>Gene Expression</topic><topic>Gene Products, env - genetics</topic><topic>Gene Products, env - immunology</topic><topic>HIV Antigens - immunology</topic><topic>HIV Core Protein p24 - genetics</topic><topic>HIV Core Protein p24 - immunology</topic><topic>HIV Infections - diagnosis</topic><topic>HIV Infections - immunology</topic><topic>HIV-1 - immunology</topic><topic>HIV-1 - pathogenicity</topic><topic>Host-Parasite Interactions</topic><topic>Human immunodeficiency virus 1</topic><topic>Humans</topic><topic>Immunodeficiencies</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>Immunopathology</topic><topic>Leukocytes, Mononuclear - immunology</topic><topic>Longitudinal Studies</topic><topic>Lymphocyte Count</topic><topic>Medical sciences</topic><topic>Recombination, Genetic</topic><topic>Survivors</topic><topic>T-Lymphocytes, Cytotoxic - immunology</topic><topic>Transformation, Genetic</topic><topic>Vaccinia virus - genetics</topic><topic>Viral Load</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BARIOU, C</creatorcontrib><creatorcontrib>GENETET, N</creatorcontrib><creatorcontrib>RUFFAULT, A</creatorcontrib><creatorcontrib>MICHELET, C</creatorcontrib><creatorcontrib>CARTIER, F</creatorcontrib><creatorcontrib>GENETET, B</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>AIDS research and human retroviruses</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BARIOU, C</au><au>GENETET, N</au><au>RUFFAULT, A</au><au>MICHELET, C</au><au>CARTIER, F</au><au>GENETET, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Longitudinal study of HIV-specific cytotoxic lymphocytes in HIV type 1-infected patients : Relative balance between host immune response and the spread of HIV type 1 infection</atitle><jtitle>AIDS research and human retroviruses</jtitle><addtitle>AIDS Res Hum Retroviruses</addtitle><date>1997-10-10</date><risdate>1997</risdate><volume>13</volume><issue>15</issue><spage>1301</spage><epage>1312</epage><pages>1301-1312</pages><issn>0889-2229</issn><eissn>1931-8405</eissn><coden>ARHRE7</coden><abstract>To evaluate the contribution of a specific cytotoxic response in the control of HIV infection in relation to clinical status, we performed serial analysis of anti-Env and anti-Gag cytotoxic activity in 13 infected individuals over a 6- to 10-year period, using cryopreserved peripheral blood mononuclear cells (PBMCs). Autologous EBV-transformed B cell lines infected in vitro with recombinant vaccinia viruses expressing HIV-1 env and gag genes were used as targets. Without any stimulation of the effector cells, we were able to show an anti-HIV cytotoxic activity in the PBMCs of 12 of 13 HIV-1-infected patients, consistent with chronic immune activation in HIV infection. Different patterns of HIV-specific cytotoxic activity were observed, and the extent of this cytotoxic response varied between the clinically defined groups of individuals. No direct relationship was observed with the number of CD4 and CD8 lymphocytes during the observation period. However, patients who remained asymptomatic had a more vigorous cytotoxic response than patients with clinical deterioration during the observation period, and a significant difference was observed for HIV Gag-specific CTL activity. From these data, we suggest that the HIV-specific cytotoxic response has a protective role in the course of HIV infection.</abstract><cop>Larchmont, NY</cop><pub>Liebert</pub><pmid>9339847</pmid><doi>10.1089/aid.1997.13.1301</doi><tpages>12</tpages></addata></record> |
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subjects | B-Lymphocytes - immunology Biological and medical sciences CD4 Lymphocyte Count CD4-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - immunology Cryopreservation Cytotoxicity Tests, Immunologic Gene Expression Gene Products, env - genetics Gene Products, env - immunology HIV Antigens - immunology HIV Core Protein p24 - genetics HIV Core Protein p24 - immunology HIV Infections - diagnosis HIV Infections - immunology HIV-1 - immunology HIV-1 - pathogenicity Host-Parasite Interactions Human immunodeficiency virus 1 Humans Immunodeficiencies Immunodeficiencies. Immunoglobulinopathies Immunopathology Leukocytes, Mononuclear - immunology Longitudinal Studies Lymphocyte Count Medical sciences Recombination, Genetic Survivors T-Lymphocytes, Cytotoxic - immunology Transformation, Genetic Vaccinia virus - genetics Viral Load |
title | Longitudinal study of HIV-specific cytotoxic lymphocytes in HIV type 1-infected patients : Relative balance between host immune response and the spread of HIV type 1 infection |
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