Source:http://linkedlifedata.com/resource/pubmed/id/11851899
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rdf:type | |
lifeskim:mentions |
umls-concept:C0042769,
umls-concept:C0205178,
umls-concept:C0205245,
umls-concept:C0220847,
umls-concept:C0242629,
umls-concept:C0392762,
umls-concept:C0524910,
umls-concept:C0871261,
umls-concept:C1514893,
umls-concept:C1704632,
umls-concept:C1705241,
umls-concept:C1705242,
umls-concept:C1706817,
umls-concept:C2699488,
umls-concept:C2911692
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pubmed:issue |
1
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pubmed:dateCreated |
2002-2-19
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pubmed:abstractText |
CD8+ T lymphocyte responses are important in the clearance of viral infections. In chronic infections they may contribute to pathogenesis. To investigate the role of CD8+ T lymphocyte responses in viral clearance and chronic hepatitis C we have compared hepatitis C virus (HCV) specific cytotoxicity and interferon-gamma (IFN-gamma) production in patients with resolved-acute, and chronic HCV infection. CD8+ T cell responses to a panel of 13 HCV T cell peptide epitopes were studied using Elispot assays of IFN-gamma production and chromium release cytotoxicity assays. Responses of seven patients with resolved acute HCV infection were compared with those of 14 chronically infected patients. HCV-specific cytotoxicity differentiated the two populations of patients. The majority (71%) of patients with resolved acute infection tested positive to 42% of relevant peptides compared with the minority (28%) of patients with chronic hepatitis C (P=0.03) who responded to only 8% of relevant peptides (P=0.0009). In contrast, HCV-specific IFN-gamma production was detected in 86% of patients with either resolved or chronic infection in response to 42% and 35%, respectively, of relevant peptides tested (not significant). In patients with chronic infection the magnitude of the HCV-specific IFN-gamma production was inversely correlated to viral load (R2=0.52; P=0.042). Failure to clear HCV infection may be attributable to the presence of noncytolytic IFN-gamma producing CD8+ T lymphocytes in chronically infected patients. However these CD8+ T cells may play a beneficial role in contributing to the control of viral load in chronic hepatitis C.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1352-0504
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
18-28
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:11851899-Acute Disease,
pubmed-meshheading:11851899-Adult,
pubmed-meshheading:11851899-Aged,
pubmed-meshheading:11851899-CD8-Positive T-Lymphocytes,
pubmed-meshheading:11851899-Cell Line, Transformed,
pubmed-meshheading:11851899-Cells, Cultured,
pubmed-meshheading:11851899-Cytotoxicity, Immunologic,
pubmed-meshheading:11851899-Epitopes, T-Lymphocyte,
pubmed-meshheading:11851899-Female,
pubmed-meshheading:11851899-Hepatitis C,
pubmed-meshheading:11851899-Hepatitis C, Chronic,
pubmed-meshheading:11851899-Humans,
pubmed-meshheading:11851899-Immunophenotyping,
pubmed-meshheading:11851899-Interferon-gamma,
pubmed-meshheading:11851899-Male,
pubmed-meshheading:11851899-Middle Aged
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pubmed:year |
2002
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pubmed:articleTitle |
Quantitative and functional differences in CD8+ lymphocyte responses in resolved acute and chronic hepatitis C virus infection.
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pubmed:affiliation |
Liver Group, Division of Infection, Inflammation and Repair, University of Southampton, Southampton, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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