Brief Reports
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jan 1, 2004; 10(1): 143-146
Published online Jan 1, 2004. doi: 10.3748/wjg.v10.i1.143
Response of TT virus to IFN plus ribavirin treatment in patients with chronic hepatitis C
Javier Moreno, Gloria Moraleda, Rafael Barcena, Mluisa Mateos, Santos del Campo
Javier Moreno, Rafael Barcena, Santos del Campo, Gloria Moraleda, Department of Gastroenterology, Hospital Ramon y Cajal, Facultad de Medicina, Universidad de Alcala, Madrid, Spain
Mluisa Mateos, Department of Microbiology, Hospital Ramon y Cajal, Madrid, Spain
Author contributions: Javier Moreno and Gloria Moraleda contributed equally to this work
Supported by Fundacion Manchega de Investigacion y Docencia en Gastroenterologia and partially by Red Nacional en Investigación de Hepatología y Gastroenterologia (RNIHG)
Correspondence to: Dr. Rafael Barcena Marugan, Department of Gastroenterology, Hospital Ramony Cajal, Ctra. Colmenar, Km 9.1, 28034 Madrid, Spain. rbarcena@hrc.insalud.es
Telephone: +34-91-3368093 Fax: +34-91-7291456
Received: August 11, 2003
Revised: August 20, 2003
Accepted: October 22, 2003
Published online: January 1, 2004
Abstract

AIM: TT virus (TTV) is a newly described DNA virus related to postransfusion hepatitis that produces persistent viremia in the absence of clinical manifestations. PEG-IFN plus ribavirin have been useful in the treatment of chronic hepatitis C infection. This study investigated the responses of TT virus (TTV) and hepatitis C virus (HCV) to PEG-IFN plus ribavirin therapy.

METHODS: Fifteen patients infected with HCV were treated with PEG-IFN(0.5 μg/body weight/week) and ribavirin (1000 mg-1200 mg/daily) for 48 weeks. Blood samples were drawn at the beginning and the end of the therapy. Serum TTV DNA and HCV RNA were quantified by real time PCR.

RESULTS: At the beginning of treatment, TTV infection was detected in 10/15 (66.6%) of HCV-infected patients. Loss of serum TTV DNA at the end of therapy occurred in 6/10 (60%) patients. Out of these 6 patients, 4 (67%) became positive for TTV DNA after 6 months of therapy. Regarding HCV viremia, 11/15 (73%) patients were negative for serum HCV RNA after 48 weeks of therapy, 7/11 (64%) of these cases also became negative for TTV DNA following the combined treatment. In the 3/4 (75%) patients who were positive for HCV RNA at the end of therapy, TTV DNA was detected as well. Sustained HCV response at 6 months after treatment was 53% (8/15).

CONCLUSION: No TTV sustained response can be achieved in any patient after PEG-IFN plus ribavirin administration.

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