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Kinetics of Cytokine Expression during Primary Human Immunodeficiency Virus Type 1 Infection
In the present study, we have determined the kinetics of constitutive expression of a panel of cytokines [interleukin (IL) 2, IL-4, IL-6, IL-10, interferon γ (IFN-γ ), and tumor necrosis factor α (TNF-α )] in sequential peripheral blood mononuclear cell samples from nine individuals with primary hum...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1996-04, Vol.93 (9), p.4386-4391 |
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creator | Graziosi, Cecilia Gantt, Kira R. Vaccarezza, Mauro Demarest, James F. Daucher, MaryBeth Saag, Michael S. Shaw, George M. Quinn, Thomas C. Cohen, Oren J. Welbon, Craig C. Pantaleo, Giuseppe Fauci, Anthony S. |
description | In the present study, we have determined the kinetics of constitutive expression of a panel of cytokines [interleukin (IL) 2, IL-4, IL-6, IL-10, interferon γ (IFN-γ ), and tumor necrosis factor α (TNF-α )] in sequential peripheral blood mononuclear cell samples from nine individuals with primary human immunodeficiency virus infection. Expression of IL-2 and IL-4 was barely detected in peripheral blood mononuclear cells. However, substantial levels of IL-2 expression were found in mononuclear cells isolated from lymph node. Expression of IL-6 was detected in only three of nine patients, and IL-6 expression was observed when transition from the acute to the chronic phase had already occurred. Expression of IL-10 and TNF-α was consistently observed in all patients tested, and levels of both cytokines were either stable or progressively increased over time. Similar to IL-10 and TNF-α , IFN-γ expression was detected in all patients; however, in five of nine patients, IFN-γ expression peaked very early during primary infection. The early peak in IFN-γ expression coincided with oligoclonal expansions of CD8+ T cells in five of six patients, and CD8+ T cells mostly accounted for the expression of this cytokine. These results indicate that high levels of expression of proinflammatory cytokines are associated with primary infection and that the cytokine response during this phase of infection is strongly influenced by oligoclonal expansions of CD8+ T cells. |
doi_str_mv | 10.1073/pnas.93.9.4386 |
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Expression of IL-2 and IL-4 was barely detected in peripheral blood mononuclear cells. However, substantial levels of IL-2 expression were found in mononuclear cells isolated from lymph node. Expression of IL-6 was detected in only three of nine patients, and IL-6 expression was observed when transition from the acute to the chronic phase had already occurred. Expression of IL-10 and TNF-α was consistently observed in all patients tested, and levels of both cytokines were either stable or progressively increased over time. Similar to IL-10 and TNF-α , IFN-γ expression was detected in all patients; however, in five of nine patients, IFN-γ expression peaked very early during primary infection. The early peak in IFN-γ expression coincided with oligoclonal expansions of CD8+ T cells in five of six patients, and CD8+ T cells mostly accounted for the expression of this cytokine. These results indicate that high levels of expression of proinflammatory cytokines are associated with primary infection and that the cytokine response during this phase of infection is strongly influenced by oligoclonal expansions of CD8+ T cells.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.93.9.4386</identifier><identifier>PMID: 8633076</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>AIDS/HIV ; Blood ; Cells, Cultured ; Cytokines ; Cytokines - biosynthesis ; Gene Expression Regulation, Viral ; HIV ; HIV Infections - immunology ; HIV-1 ; Human immunodeficiency virus ; human immunodeficiency virus 1 ; Humans ; Immune response ; Immunity (Disease) ; Infections ; Interferon-gamma - biosynthesis ; Interleukin-10 - biosynthesis ; Interleukin-2 - biosynthesis ; Interleukin-4 - biosynthesis ; Interleukin-6 - biosynthesis ; Kinetics ; Lymph nodes ; Lymph Nodes - immunology ; Lymphocytes - immunology ; Receptors, Antigen, T-Cell, alpha-beta ; RNA, Messenger - analysis ; RNA, Messenger - biosynthesis ; Symptoms ; T lymphocytes ; T-Lymphocyte Subsets - immunology ; Time Factors ; Tumor Necrosis Factor-alpha - biosynthesis ; Viremia</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1996-04, Vol.93 (9), p.4386-4391</ispartof><rights>Copyright 1996 National Academy of Sciences</rights><rights>Copyright National Academy of Sciences Apr 30, 1996</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-55733b772838a8cf14936905de197d91975dfd8adb741f708375252658622ed23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/93/9.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/39255$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/39255$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8633076$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Graziosi, Cecilia</creatorcontrib><creatorcontrib>Gantt, Kira R.</creatorcontrib><creatorcontrib>Vaccarezza, Mauro</creatorcontrib><creatorcontrib>Demarest, James F.</creatorcontrib><creatorcontrib>Daucher, MaryBeth</creatorcontrib><creatorcontrib>Saag, Michael S.</creatorcontrib><creatorcontrib>Shaw, George M.</creatorcontrib><creatorcontrib>Quinn, Thomas C.</creatorcontrib><creatorcontrib>Cohen, Oren J.</creatorcontrib><creatorcontrib>Welbon, Craig C.</creatorcontrib><creatorcontrib>Pantaleo, Giuseppe</creatorcontrib><creatorcontrib>Fauci, Anthony S.</creatorcontrib><title>Kinetics of Cytokine Expression during Primary Human Immunodeficiency Virus Type 1 Infection</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>In the present study, we have determined the kinetics of constitutive expression of a panel of cytokines [interleukin (IL) 2, IL-4, IL-6, IL-10, interferon γ (IFN-γ ), and tumor necrosis factor α (TNF-α )] in sequential peripheral blood mononuclear cell samples from nine individuals with primary human immunodeficiency virus infection. Expression of IL-2 and IL-4 was barely detected in peripheral blood mononuclear cells. However, substantial levels of IL-2 expression were found in mononuclear cells isolated from lymph node. Expression of IL-6 was detected in only three of nine patients, and IL-6 expression was observed when transition from the acute to the chronic phase had already occurred. Expression of IL-10 and TNF-α was consistently observed in all patients tested, and levels of both cytokines were either stable or progressively increased over time. Similar to IL-10 and TNF-α , IFN-γ expression was detected in all patients; however, in five of nine patients, IFN-γ expression peaked very early during primary infection. The early peak in IFN-γ expression coincided with oligoclonal expansions of CD8+ T cells in five of six patients, and CD8+ T cells mostly accounted for the expression of this cytokine. These results indicate that high levels of expression of proinflammatory cytokines are associated with primary infection and that the cytokine response during this phase of infection is strongly influenced by oligoclonal expansions of CD8+ T cells.</description><subject>AIDS/HIV</subject><subject>Blood</subject><subject>Cells, Cultured</subject><subject>Cytokines</subject><subject>Cytokines - biosynthesis</subject><subject>Gene Expression Regulation, Viral</subject><subject>HIV</subject><subject>HIV Infections - immunology</subject><subject>HIV-1</subject><subject>Human immunodeficiency virus</subject><subject>human immunodeficiency virus 1</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immunity (Disease)</subject><subject>Infections</subject><subject>Interferon-gamma - biosynthesis</subject><subject>Interleukin-10 - biosynthesis</subject><subject>Interleukin-2 - biosynthesis</subject><subject>Interleukin-4 - biosynthesis</subject><subject>Interleukin-6 - biosynthesis</subject><subject>Kinetics</subject><subject>Lymph nodes</subject><subject>Lymph Nodes - immunology</subject><subject>Lymphocytes - immunology</subject><subject>Receptors, Antigen, T-Cell, alpha-beta</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Symptoms</subject><subject>T lymphocytes</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>Time Factors</subject><subject>Tumor Necrosis Factor-alpha - biosynthesis</subject><subject>Viremia</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNqFkc9rFDEYhoModa1ePQhC8NDbjPk5ScCLLLVdLOihehLCbCZTs84kYzKR7n_fLLsuqwe9JIT3ecKXvAC8xKjGSNC3k29TrWitakZl8wgsMFK4aphCj8ECISIqyQh7Cp6ltEEIKS7RGTiTDaVINAvw7aPzdnYmwdDD5XYOP8oZXt5P0abkgoddjs7fwc_RjW3cwus8th6uxjH70NneGWe92cKvLuYEb7eThRiufG_NXOTn4EnfDsm-OOzn4MuHy9vldXXz6Wq1fH9TGY7pXHEuKF0LQSSVrTQ9Zoo2CvHOYiU6VRbe9Z1su7VguBdIUsEJJw2XDSG2I_QcvNvfO-X1aDtj_RzbQU_7mXVonf4z8e67vgu_NFWciaJfHPQYfmabZj26ZOwwtN6GnLSQiBLG-H9BLJBgDOMCvvkL3IQcffkDTRCmHCuOClTvIRNDStH2x4Ex0rtu9a5brahWetdtEV6fPvOIH8o8yXfe7_TUv_hXrvs8DLO9nwv4ag9u0hzikaSKcE4fAJlZwF4</recordid><startdate>19960430</startdate><enddate>19960430</enddate><creator>Graziosi, Cecilia</creator><creator>Gantt, Kira R.</creator><creator>Vaccarezza, Mauro</creator><creator>Demarest, James F.</creator><creator>Daucher, MaryBeth</creator><creator>Saag, Michael S.</creator><creator>Shaw, George M.</creator><creator>Quinn, Thomas C.</creator><creator>Cohen, Oren J.</creator><creator>Welbon, Craig C.</creator><creator>Pantaleo, Giuseppe</creator><creator>Fauci, Anthony S.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19960430</creationdate><title>Kinetics of Cytokine Expression during Primary Human Immunodeficiency Virus Type 1 Infection</title><author>Graziosi, Cecilia ; 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Expression of IL-2 and IL-4 was barely detected in peripheral blood mononuclear cells. However, substantial levels of IL-2 expression were found in mononuclear cells isolated from lymph node. Expression of IL-6 was detected in only three of nine patients, and IL-6 expression was observed when transition from the acute to the chronic phase had already occurred. Expression of IL-10 and TNF-α was consistently observed in all patients tested, and levels of both cytokines were either stable or progressively increased over time. Similar to IL-10 and TNF-α , IFN-γ expression was detected in all patients; however, in five of nine patients, IFN-γ expression peaked very early during primary infection. The early peak in IFN-γ expression coincided with oligoclonal expansions of CD8+ T cells in five of six patients, and CD8+ T cells mostly accounted for the expression of this cytokine. These results indicate that high levels of expression of proinflammatory cytokines are associated with primary infection and that the cytokine response during this phase of infection is strongly influenced by oligoclonal expansions of CD8+ T cells.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>8633076</pmid><doi>10.1073/pnas.93.9.4386</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | AIDS/HIV Blood Cells, Cultured Cytokines Cytokines - biosynthesis Gene Expression Regulation, Viral HIV HIV Infections - immunology HIV-1 Human immunodeficiency virus human immunodeficiency virus 1 Humans Immune response Immunity (Disease) Infections Interferon-gamma - biosynthesis Interleukin-10 - biosynthesis Interleukin-2 - biosynthesis Interleukin-4 - biosynthesis Interleukin-6 - biosynthesis Kinetics Lymph nodes Lymph Nodes - immunology Lymphocytes - immunology Receptors, Antigen, T-Cell, alpha-beta RNA, Messenger - analysis RNA, Messenger - biosynthesis Symptoms T lymphocytes T-Lymphocyte Subsets - immunology Time Factors Tumor Necrosis Factor-alpha - biosynthesis Viremia |
title | Kinetics of Cytokine Expression during Primary Human Immunodeficiency Virus Type 1 Infection |
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