Loading…

Cellular Immune Responses against Hepatitis C Virus

Cellular immune responses are typically important in recovery from acute infections, and studies of acute hepatitis C confirm that broadly directed CD4+ and CD8+ T cell responses are associated with spontaneous clearance of infection. However, a major unanswered question is what role the cellular im...

Full description

Saved in:
Bibliographic Details
Published in:Clinical infectious diseases 2005-07, Vol.41 (Supplement-1), p.S25-S31
Main Author: Koziel, Margaret James
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c426t-df92914b6ecccd89e66ff9be38d85a80b80122bd0c80be10458864e06291a7393
cites cdi_FETCH-LOGICAL-c426t-df92914b6ecccd89e66ff9be38d85a80b80122bd0c80be10458864e06291a7393
container_end_page S31
container_issue Supplement-1
container_start_page S25
container_title Clinical infectious diseases
container_volume 41
creator Koziel, Margaret James
description Cellular immune responses are typically important in recovery from acute infections, and studies of acute hepatitis C confirm that broadly directed CD4+ and CD8+ T cell responses are associated with spontaneous clearance of infection. However, a major unanswered question is what role the cellular immune response plays in progression of liver disease during chronic infection. Classic models of hepatitis C suggest that cellular immune responses promote liver injury, either by causing direct cytolysis of infected cells or by promoting inflammation. However, clinical evidence suggests that persons with cellular immune dysfunction, such as that due to with human immunodeficiency virus (HIV) infection, have more-rapid disease progression. Recent data suggest that cellular immune responses do serve to limit the progression of liver disease, even if they are ineffective at clearance of virus. There is limited information on the effect of HIV coinfection on the cellular immune response to hepatitis C virus, but further study of this issue might shed light on the pathogenesis of liver disease in both immunocompromised and nonimmunocompromised hosts.
doi_str_mv 10.1086/429492
format article
fullrecord <record><control><sourceid>jstor_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_68753394</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>4463316</jstor_id><sourcerecordid>4463316</sourcerecordid><originalsourceid>FETCH-LOGICAL-c426t-df92914b6ecccd89e66ff9be38d85a80b80122bd0c80be10458864e06291a7393</originalsourceid><addsrcrecordid>eNqFkE9Lw0AQxRdRbK36CUSCB2_R_Z_dowS1lYIiWqSXZZNMJLVJ6m4C-u1daWnBi6d58H7zmHkInRJ8RbCS15xqrukeGhLBklgKTfaDxkLFXDE1QEfeLzAmRGFxiAZEUikkwUPEUlgu-6V10aSu-waiZ_CrtvHgI_tuq8Z30RhWtqu6ykdpNKtc74_RQWmXHk42c4Re725f0nE8fbyfpDfTOOdUdnFRaqoJzyTkeV4oDVKWpc6AqUIJq3CmMKE0K3AeNBDMhVKSA5ZhyyZMsxG6XOeuXPvZg-9MXfk83GsbaHtvpEoEY5r_C5JEYK0ZC-DFH3DR9q4JTxhKtJZYM7pLy13rvYPSrFxVW_dtCDa_ZZt12QE836T1WQ3FDtu0G4CzNbDwXeu2PueSMSKDHa_tynfwtbWt-zAyYYkw47e5mT3NU0EVMw_sB9y-jos</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>219960932</pqid></control><display><type>article</type><title>Cellular Immune Responses against Hepatitis C Virus</title><source>JSTOR Archival Journals and Primary Sources Collection</source><source>Oxford Journals Online</source><creator>Koziel, Margaret James</creator><creatorcontrib>Koziel, Margaret James</creatorcontrib><description>Cellular immune responses are typically important in recovery from acute infections, and studies of acute hepatitis C confirm that broadly directed CD4+ and CD8+ T cell responses are associated with spontaneous clearance of infection. However, a major unanswered question is what role the cellular immune response plays in progression of liver disease during chronic infection. Classic models of hepatitis C suggest that cellular immune responses promote liver injury, either by causing direct cytolysis of infected cells or by promoting inflammation. However, clinical evidence suggests that persons with cellular immune dysfunction, such as that due to with human immunodeficiency virus (HIV) infection, have more-rapid disease progression. Recent data suggest that cellular immune responses do serve to limit the progression of liver disease, even if they are ineffective at clearance of virus. There is limited information on the effect of HIV coinfection on the cellular immune response to hepatitis C virus, but further study of this issue might shed light on the pathogenesis of liver disease in both immunocompromised and nonimmunocompromised hosts.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1086/429492</identifier><identifier>PMID: 16265610</identifier><language>eng</language><publisher>United States: The University of Chicago Press</publisher><subject>Animals ; Blood ; CD4-Positive T-Lymphocytes - immunology ; CD4-Positive T-Lymphocytes - virology ; CD8-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - virology ; Chronic hepatitis ; Cytokines ; Hepacivirus ; Hepacivirus - immunology ; Hepatitis ; Hepatitis C ; Hepatitis C - complications ; Hepatitis C - immunology ; Hepatitis C virus ; Hepatitis C, Chronic - immunology ; HIV ; HIV Infections - complications ; HIV Infections - immunology ; Human immunodeficiency virus ; Humans ; Immune system ; Immunity, Cellular - immunology ; Infections ; Killer Cells, Natural - immunology ; Liver ; Mice ; T lymphocytes ; Viruses</subject><ispartof>Clinical infectious diseases, 2005-07, Vol.41 (Supplement-1), p.S25-S31</ispartof><rights>Copyright 2005 The Infectious Diseases Society of America</rights><rights>Copyright University of Chicago, acting through its Press Jul 1, 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-df92914b6ecccd89e66ff9be38d85a80b80122bd0c80be10458864e06291a7393</citedby><cites>FETCH-LOGICAL-c426t-df92914b6ecccd89e66ff9be38d85a80b80122bd0c80be10458864e06291a7393</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4463316$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4463316$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16265610$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koziel, Margaret James</creatorcontrib><title>Cellular Immune Responses against Hepatitis C Virus</title><title>Clinical infectious diseases</title><addtitle>Clinical Infectious Diseases</addtitle><description>Cellular immune responses are typically important in recovery from acute infections, and studies of acute hepatitis C confirm that broadly directed CD4+ and CD8+ T cell responses are associated with spontaneous clearance of infection. However, a major unanswered question is what role the cellular immune response plays in progression of liver disease during chronic infection. Classic models of hepatitis C suggest that cellular immune responses promote liver injury, either by causing direct cytolysis of infected cells or by promoting inflammation. However, clinical evidence suggests that persons with cellular immune dysfunction, such as that due to with human immunodeficiency virus (HIV) infection, have more-rapid disease progression. Recent data suggest that cellular immune responses do serve to limit the progression of liver disease, even if they are ineffective at clearance of virus. There is limited information on the effect of HIV coinfection on the cellular immune response to hepatitis C virus, but further study of this issue might shed light on the pathogenesis of liver disease in both immunocompromised and nonimmunocompromised hosts.</description><subject>Animals</subject><subject>Blood</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD4-Positive T-Lymphocytes - virology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - virology</subject><subject>Chronic hepatitis</subject><subject>Cytokines</subject><subject>Hepacivirus</subject><subject>Hepacivirus - immunology</subject><subject>Hepatitis</subject><subject>Hepatitis C</subject><subject>Hepatitis C - complications</subject><subject>Hepatitis C - immunology</subject><subject>Hepatitis C virus</subject><subject>Hepatitis C, Chronic - immunology</subject><subject>HIV</subject><subject>HIV Infections - complications</subject><subject>HIV Infections - immunology</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immune system</subject><subject>Immunity, Cellular - immunology</subject><subject>Infections</subject><subject>Killer Cells, Natural - immunology</subject><subject>Liver</subject><subject>Mice</subject><subject>T lymphocytes</subject><subject>Viruses</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkE9Lw0AQxRdRbK36CUSCB2_R_Z_dowS1lYIiWqSXZZNMJLVJ6m4C-u1daWnBi6d58H7zmHkInRJ8RbCS15xqrukeGhLBklgKTfaDxkLFXDE1QEfeLzAmRGFxiAZEUikkwUPEUlgu-6V10aSu-waiZ_CrtvHgI_tuq8Z30RhWtqu6ykdpNKtc74_RQWmXHk42c4Re725f0nE8fbyfpDfTOOdUdnFRaqoJzyTkeV4oDVKWpc6AqUIJq3CmMKE0K3AeNBDMhVKSA5ZhyyZMsxG6XOeuXPvZg-9MXfk83GsbaHtvpEoEY5r_C5JEYK0ZC-DFH3DR9q4JTxhKtJZYM7pLy13rvYPSrFxVW_dtCDa_ZZt12QE836T1WQ3FDtu0G4CzNbDwXeu2PueSMSKDHa_tynfwtbWt-zAyYYkw47e5mT3NU0EVMw_sB9y-jos</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Koziel, Margaret James</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><general>Oxford University Press</general><scope>BSCLL</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>7QL</scope><scope>7T2</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20050701</creationdate><title>Cellular Immune Responses against Hepatitis C Virus</title><author>Koziel, Margaret James</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-df92914b6ecccd89e66ff9be38d85a80b80122bd0c80be10458864e06291a7393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Blood</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD4-Positive T-Lymphocytes - virology</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - virology</topic><topic>Chronic hepatitis</topic><topic>Cytokines</topic><topic>Hepacivirus</topic><topic>Hepacivirus - immunology</topic><topic>Hepatitis</topic><topic>Hepatitis C</topic><topic>Hepatitis C - complications</topic><topic>Hepatitis C - immunology</topic><topic>Hepatitis C virus</topic><topic>Hepatitis C, Chronic - immunology</topic><topic>HIV</topic><topic>HIV Infections - complications</topic><topic>HIV Infections - immunology</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immune system</topic><topic>Immunity, Cellular - immunology</topic><topic>Infections</topic><topic>Killer Cells, Natural - immunology</topic><topic>Liver</topic><topic>Mice</topic><topic>T lymphocytes</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koziel, Margaret James</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koziel, Margaret James</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellular Immune Responses against Hepatitis C Virus</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clinical Infectious Diseases</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>41</volume><issue>Supplement-1</issue><spage>S25</spage><epage>S31</epage><pages>S25-S31</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><abstract>Cellular immune responses are typically important in recovery from acute infections, and studies of acute hepatitis C confirm that broadly directed CD4+ and CD8+ T cell responses are associated with spontaneous clearance of infection. However, a major unanswered question is what role the cellular immune response plays in progression of liver disease during chronic infection. Classic models of hepatitis C suggest that cellular immune responses promote liver injury, either by causing direct cytolysis of infected cells or by promoting inflammation. However, clinical evidence suggests that persons with cellular immune dysfunction, such as that due to with human immunodeficiency virus (HIV) infection, have more-rapid disease progression. Recent data suggest that cellular immune responses do serve to limit the progression of liver disease, even if they are ineffective at clearance of virus. There is limited information on the effect of HIV coinfection on the cellular immune response to hepatitis C virus, but further study of this issue might shed light on the pathogenesis of liver disease in both immunocompromised and nonimmunocompromised hosts.</abstract><cop>United States</cop><pub>The University of Chicago Press</pub><pmid>16265610</pmid><doi>10.1086/429492</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1058-4838
ispartof Clinical infectious diseases, 2005-07, Vol.41 (Supplement-1), p.S25-S31
issn 1058-4838
1537-6591
language eng
recordid cdi_proquest_miscellaneous_68753394
source JSTOR Archival Journals and Primary Sources Collection; Oxford Journals Online
subjects Animals
Blood
CD4-Positive T-Lymphocytes - immunology
CD4-Positive T-Lymphocytes - virology
CD8-Positive T-Lymphocytes - immunology
CD8-Positive T-Lymphocytes - virology
Chronic hepatitis
Cytokines
Hepacivirus
Hepacivirus - immunology
Hepatitis
Hepatitis C
Hepatitis C - complications
Hepatitis C - immunology
Hepatitis C virus
Hepatitis C, Chronic - immunology
HIV
HIV Infections - complications
HIV Infections - immunology
Human immunodeficiency virus
Humans
Immune system
Immunity, Cellular - immunology
Infections
Killer Cells, Natural - immunology
Liver
Mice
T lymphocytes
Viruses
title Cellular Immune Responses against Hepatitis C Virus
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T11%3A29%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cellular%20Immune%20Responses%20against%20Hepatitis%20C%20Virus&rft.jtitle=Clinical%20infectious%20diseases&rft.au=Koziel,%20Margaret%20James&rft.date=2005-07-01&rft.volume=41&rft.issue=Supplement-1&rft.spage=S25&rft.epage=S31&rft.pages=S25-S31&rft.issn=1058-4838&rft.eissn=1537-6591&rft_id=info:doi/10.1086/429492&rft_dat=%3Cjstor_proqu%3E4463316%3C/jstor_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c426t-df92914b6ecccd89e66ff9be38d85a80b80122bd0c80be10458864e06291a7393%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=219960932&rft_id=info:pmid/16265610&rft_jstor_id=4463316&rfr_iscdi=true