Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9244297 | Gastroenterology | 2005 | 8 Pages |
Abstract
Background & Aims: Hepatitis C virus (HCV) infects millions of people worldwide. Therapy is limited, and treatment does not produce a sustained response in the majority of patients. Development of new agents has been hampered by the lack of a convenient animal model. The aim of this study was to determine whether an immunocompetent rat, tolerized and transplanted with a human hepatoma cell line (Huh 7 cells), could be used to sustain an HCV infection. Methods: Fetal rats were tolerized in utero with 105 Huh 7 cells. One day after birth, rats were transplanted with 5 Ã 106 Huh 7 cells and, a week later, inoculated with HCV, genotype 1. Results: In tolerized, transplanted, and HCV-infected rats, Huh 7 cells were found in the liver, and HCV viral replication was detected by the presence of negative strand HCV RNA. HCV levels in serum were measured at 11,000 copies/mL at week 4, peaked at 22,500 copies/mL by week 12. In tolerized, transplanted, inoculated rats, but not controls, serum alanine aminotransferase (ALT) values increased to 60 IU/L by week 4 and reached a peak of approximately 120 IU/L by week 13. Histology showed foci of mononuclear infiltrates in portal and central regions. Conclusions: HCV-inoculated immunocompetent rats tolerized and transplanted with Huh 7 cells support HCV gene expression, viral replication, and develop biochemical and histologic evidence of hepatitis.
Related Topics
Health Sciences
Medicine and Dentistry
Gastroenterology
Authors
George Y. Wu, Masayoshi Konishi, Cherie M. Walton, Denise Olive, Kazuhiko Hayashi, Catherine H. Wu,