Sustained virological response after early antiviral treatment of acute hepatitis C virus and HIV coinfection.

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Sustained virological response after early antiviral treatment of acute hepatitis C virus and HIV coinfection. / Schulze Zur Wiesch, Julian; Pieper, Dorothea; Stahmer, Ingrid; Eiermann, Thomas; Buggisch, Peter; Lohse, Ansgar W.; Hauber, Joachim; van Lunzen, Jan.

in: CLIN INFECT DIS, Jahrgang 49, Nr. 3, 3, 2009, S. 466-472.

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@article{0c559e20ae824693b3f1079a541b2ef5,
title = "Sustained virological response after early antiviral treatment of acute hepatitis C virus and HIV coinfection.",
abstract = "BACKGROUND: Limited data exist describing the clinical outcome and immunological response primed during simultaneously acquired acute hepatitis C virus (HCV) and human immunodeficiency virus (HIV) coinfection. We present detailed clinical and immunological analysis of 3 individuals after concomitant infection with acute HCV and primary HIV. METHODS: In addition to longitudinal clinical parameters, virus-specific T cell responses were assessed using Elispot, standard proliferative (carboxyfluorescein diacetate succinimidyl ester), and in vitro CD4(+) T cell assays. RESULTS: In all patients, anti-HCV treatment was started with pegylated interferon-alpha, and antiretroviral therapy was coadministered early during primary infection. HCV viremia was cleared under therapy with pegylated interferon-alpha in all 3 cases. In 2 patients, HIV replication was contained even after antiretroviral therapy had been interrupted, which was associated with strong HIV-specific CD8(+) and CD4(+) T cell responses. In these 2 patients, multispecific HCV CD4(+) T cell responses could also be detected. No HCV-specific CD4(+) T cell responses were detected in the third patient, who also had the lowest nadir CD4(+) cell count during primary HIV infection (",
author = "{Schulze Zur Wiesch}, Julian and Dorothea Pieper and Ingrid Stahmer and Thomas Eiermann and Peter Buggisch and Lohse, {Ansgar W.} and Joachim Hauber and {van Lunzen}, Jan",
year = "2009",
language = "Deutsch",
volume = "49",
pages = "466--472",
journal = "CLIN INFECT DIS",
issn = "1058-4838",
publisher = "Oxford University Press",
number = "3",

}

RIS

TY - JOUR

T1 - Sustained virological response after early antiviral treatment of acute hepatitis C virus and HIV coinfection.

AU - Schulze Zur Wiesch, Julian

AU - Pieper, Dorothea

AU - Stahmer, Ingrid

AU - Eiermann, Thomas

AU - Buggisch, Peter

AU - Lohse, Ansgar W.

AU - Hauber, Joachim

AU - van Lunzen, Jan

PY - 2009

Y1 - 2009

N2 - BACKGROUND: Limited data exist describing the clinical outcome and immunological response primed during simultaneously acquired acute hepatitis C virus (HCV) and human immunodeficiency virus (HIV) coinfection. We present detailed clinical and immunological analysis of 3 individuals after concomitant infection with acute HCV and primary HIV. METHODS: In addition to longitudinal clinical parameters, virus-specific T cell responses were assessed using Elispot, standard proliferative (carboxyfluorescein diacetate succinimidyl ester), and in vitro CD4(+) T cell assays. RESULTS: In all patients, anti-HCV treatment was started with pegylated interferon-alpha, and antiretroviral therapy was coadministered early during primary infection. HCV viremia was cleared under therapy with pegylated interferon-alpha in all 3 cases. In 2 patients, HIV replication was contained even after antiretroviral therapy had been interrupted, which was associated with strong HIV-specific CD8(+) and CD4(+) T cell responses. In these 2 patients, multispecific HCV CD4(+) T cell responses could also be detected. No HCV-specific CD4(+) T cell responses were detected in the third patient, who also had the lowest nadir CD4(+) cell count during primary HIV infection (

AB - BACKGROUND: Limited data exist describing the clinical outcome and immunological response primed during simultaneously acquired acute hepatitis C virus (HCV) and human immunodeficiency virus (HIV) coinfection. We present detailed clinical and immunological analysis of 3 individuals after concomitant infection with acute HCV and primary HIV. METHODS: In addition to longitudinal clinical parameters, virus-specific T cell responses were assessed using Elispot, standard proliferative (carboxyfluorescein diacetate succinimidyl ester), and in vitro CD4(+) T cell assays. RESULTS: In all patients, anti-HCV treatment was started with pegylated interferon-alpha, and antiretroviral therapy was coadministered early during primary infection. HCV viremia was cleared under therapy with pegylated interferon-alpha in all 3 cases. In 2 patients, HIV replication was contained even after antiretroviral therapy had been interrupted, which was associated with strong HIV-specific CD8(+) and CD4(+) T cell responses. In these 2 patients, multispecific HCV CD4(+) T cell responses could also be detected. No HCV-specific CD4(+) T cell responses were detected in the third patient, who also had the lowest nadir CD4(+) cell count during primary HIV infection (

M3 - SCORING: Zeitschriftenaufsatz

VL - 49

SP - 466

EP - 472

JO - CLIN INFECT DIS

JF - CLIN INFECT DIS

SN - 1058-4838

IS - 3

M1 - 3

ER -