2009
DOI: 10.1086/600399
|View full text |Cite
|
Sign up to set email alerts
|

Sustained Virological Response after Early Antiviral Treatment of Acute Hepatitis C Virus and HIV Coinfection

Abstract: Anti-HIV and -HCV therapy should be considered early in cases of concomitant acute HCV and HIV coinfection, because successful therapy of HCV viremia seems possible even during primary HIV infection. HCV-specific T cell immunity is generated during primary HIV infection and can be preserved by HCV treatment. However, the optimal treatment algorithm needs to be established in prospective, randomized trials.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
8
0

Year Published

2010
2010
2013
2013

Publication Types

Select...
7

Relationship

2
5

Authors

Journals

citations
Cited by 8 publications
(8 citation statements)
references
References 36 publications
(58 reference statements)
0
8
0
Order By: Relevance
“…Lymphocyte proliferation assays were performed as described previously (Day et al, 2002; Lauer et al, 2002) using c22.3, c33c, c100.3, C200 and NS5 HCV proteins (Chiron) at concentrations of 10 µg/ml (Day et al, 2002). CFSE proliferation assays were performed as previously described (Lichterfeld et al, 2004; Kasprowicz et al, 2008; Schulze Zur Wiesch et al, 2009). Where indicated, IL-2–neutralizing antibodies (clone MQ1-17H12; BD) or isotype control antibodies (clone A4A; Neomarkers) were added at 10 µg/ml.…”
Section: Methodsmentioning
confidence: 99%
“…Lymphocyte proliferation assays were performed as described previously (Day et al, 2002; Lauer et al, 2002) using c22.3, c33c, c100.3, C200 and NS5 HCV proteins (Chiron) at concentrations of 10 µg/ml (Day et al, 2002). CFSE proliferation assays were performed as previously described (Lichterfeld et al, 2004; Kasprowicz et al, 2008; Schulze Zur Wiesch et al, 2009). Where indicated, IL-2–neutralizing antibodies (clone MQ1-17H12; BD) or isotype control antibodies (clone A4A; Neomarkers) were added at 10 µg/ml.…”
Section: Methodsmentioning
confidence: 99%
“… Assessment of HCV in people with hemophilia should include: anti-HCV serology to determine exposure HCV polymerase chain reaction (PCR) in those who are anti-HCV positive HCV genotyping in those who are HCV PCR positive liver function tests and non-invasive assessment of fibrosis and liver architecture The current standard of treatment for HCV is pegylated interferon (PEG-INF) and ribavirin, which give sustained virological response in 61% of people with hemophilia. (Level 1) [ ] New antiviral therapies, in combination with these drugs, may improve sustained virologic response rates. [] HCV genotype 1 and HIV coinfection predict poorer response to anti-HCV therapy. Where HCV eradication cannot be achieved, regular monitoring (every 6–12 months) for end-stage liver complication is recommended.…”
Section: Complications Of Hemophiliamentioning
confidence: 99%
“…RVR had a 100% positive predictive value, suggesting that RVR is an important predictor of SVR in acute and chronic HCV infection. Results for three patients suggest that an SVR is possible even during primary HIV infection [106]. …”
Section: Treatment Of Hcv In Co-infected Patientsmentioning
confidence: 99%