Source:http://linkedlifedata.com/resource/pubmed/id/12858407
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2003-7-14
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pubmed:abstractText |
The aim of this study was to examine whether hepatitis C virus (HCV) pretreatment quasispecies complexity was linked to virological response or other clinical and biological parameters, in human immunodeficiency virus (HIV)-coinfected patients undergoing anti-HCV treatment. In addition, HCV quasispecies composition is described longitudinally in these patients before, during, and after treatment. The 52 HIV-coinfected patients were included in a randomized therapeutic trial. At inclusion, they had CD4(+) counts of >250/micro l, HIV plasma load of <10,000 copies/ml, and chronic HCV infection with genotype 1 (n = 27), 2 (n = 2) or 3 (n = 23). These values were compared at baseline with 32 HCV-only-infected, interferon-naive patients who were infected with genotype 1, 2, or 3 (n = 16, 1, or 15, respectively). HCV complexity was studied by single-strand conformation polymorphism (SSCP) in E2 hypervariable region 1 (HVR1), and diversity was evaluated at inclusion in 20 coinfected patients by sequencing four major SSCP bands. The baseline number of SSCP bands was identical in HIV-infected and control patients. In HIV-infected patients, HCV complexity was not predictive of sustained virological response to anti-HCV treatment and was unrelated to epidemiological factors, immunological parameters linked to HIV infection (CD4(+) counts, T CD4(+) proliferative responses to HIV-1 p24), protease inhibitor treatment, HCV plasma load, or genotype. HCV diversity was lower in genotype 2- and 3-infected patients. Six months after completion of the anti-HCV treatment, in comparison with baseline, SSCP profiles were modified in 13 of the 21 nonresponding coinfected patients with analyzable samples. In conclusion, in HIV-infected patients, HCV variability had no significant influence on virological response to anti-HCV treatment.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0146-6615
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pubmed:author |
pubmed-author:ChittyIsabelleI,
pubmed-author:DuponMichelM,
pubmed-author:FleuryHervéH,
pubmed-author:GalperineTatianaT,
pubmed-author:JouvencelAnne-ChristineAC,
pubmed-author:LacutJean-YvesJY,
pubmed-author:LafonMarie-EdithME,
pubmed-author:Le BailBrigitteB,
pubmed-author:LegrandElisabethE,
pubmed-author:MorlatPhilippeP,
pubmed-author:NeauDidierD,
pubmed-author:RagnaudJean-MarieJM,
pubmed-author:TrimouletPascaleP,
pubmed-author:VenturaMichelM
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pubmed:copyrightInfo |
Copyright 2003 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:volume |
71
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
41-8
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:12858407-AIDS-Related Opportunistic Infections,
pubmed-meshheading:12858407-Adolescent,
pubmed-meshheading:12858407-Adult,
pubmed-meshheading:12858407-Female,
pubmed-meshheading:12858407-Genetic Variation,
pubmed-meshheading:12858407-Genotype,
pubmed-meshheading:12858407-HIV Infections,
pubmed-meshheading:12858407-Hepacivirus,
pubmed-meshheading:12858407-Hepatitis C, Chronic,
pubmed-meshheading:12858407-Humans,
pubmed-meshheading:12858407-Male,
pubmed-meshheading:12858407-Middle Aged,
pubmed-meshheading:12858407-Polymorphism, Single-Stranded Conformational
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pubmed:year |
2003
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pubmed:articleTitle |
Hepatitis C virus genetic variability in 52 human immunodeficiency virus-coinfected patients.
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pubmed:affiliation |
Virology Laboratory, University of Victor Segalen, Bordeaux, France. didier.neau@chu-bordeaux.fr
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't
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