Brief Reports
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Mar 1, 2004; 10(5): 733-736
Published online Mar 1, 2004. doi: 10.3748/wjg.v10.i5.733
Effect of in vitro interferon-beta administration on hepatitis C virus in peripheral blood mononuclear cells as a predictive marker of clinical response to interferon treatment for chronic hepatitis C
Kaori Mochizuki, Tatehiro Kagawa, Shinji Takashimizu, Kazuya Kawazoe, Sei-Ichiro Kojima, Naruhiko Nagata, Atsushi Nakano, Yasuhiro Nishizaki, Koichi Shiraishi, Masaru Itakura, Norihito Watanabe, Tetsuya Mine, Shohei Matsuzaki
Kaori Mochizuki, Tatehiro Kagawa, Shinji Takashimizu, Kazuya Kawazoe, Sei-Ichiro Kojima, Naruhiko Nagata, Atsushi Nakano, Yasuhiro Nishizaki, Koichi Shiraishi, Masaru Itakura, Norihito Watanabe, Tetsuya Mine, Shohei Matsuzaki, Department of Internal Medicine, Division of Gastroenterology, Tokai University School of Medicine, Bohseidai, Isehara 259-1193, Japan
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Tatehiro Kagawa, Department of Internal Medicine, Division of Gastroenterology, Tokai University School of Medicine, Bohseidai, Isehara 259-1193, Japan. kagawa@is.icc.u-tokai.ac.jp
Telephone: +81-463-93-1121
Received: October 8, 2003
Revised: December 23, 2003
Accepted: December 30, 2003
Published online: March 1, 2004
Abstract

AIM: To test whether in vitro incubation of peripheral blood mononuclear cells (PBMC) with interferon (IFN) could efficiently decrease hepatitis C virus-RNA (HCV-RNA) amount and to analyze whether this effect was associated with clinical response to IFN.

METHODS: Twenty-seven patients with histologically proven chronic hepatitis C were given intravenous administration of 6 million units (MU) IFN-β daily for 6 weeks followed by three times weekly for 20 weeks. PBMC collected before IFN therapy were incubated with IFN-β and HCV-RNA in PMBC was semi-quantitatively determined.

RESULTS: Twenty-five patients completed IFN therapy. Eight patients (32%) had sustained loss of serum HCV-RNA with normal serum ALT levels after IFN therapy (complete responders). HCV-RNA in PBMC was detected in all patients, whereas it was not detected in PBMC from healthy subjects. In vitro administration of IFN-β decreased the amount of HCV-RNA in PMBC in 18 patients (72%). Eight of these patients obtained complete response. On the other hand, none of the patients whose HCV-RNA in PBMC did not decrease by IFN-β was complete responders. Multiple logistic regression analysis revealed that the decrease of HCV-RNA amount in PBMC by IFN-β was the only independent predictor for complete response (P < 0.05).

CONCLUSION: The effect of in vitro IFN-β on HCV in PBMC reflects clinical response and would be taken into account as a predictive marker of IFN therapy for chronic hepatitis C.

Keywords: $[Keywords]