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A Cell Culture Model for Producing High Titer Hepatitis E Virus Stocks
Published on: June 26, 2020
[HGV and TTV - new hepatitis viruses]
Insights
Hepatitis G virus (HGV) and TT virus (TTV) infections were found in nearly 20% and 12% of chronic liver disease patients, respectively. Their exact role in liver disease and treatment efficacy require further investigation.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Chronic hepatic diseases (CHD) present complex etiological challenges.
- Hepatitis G virus (HGV) and TT virus (TTV) are emerging viral agents with incompletely understood roles in liver pathology.
Purpose of the Study:
- To investigate the clinical, immunological, and morphological characteristics of HGV and TTV infections in patients with CHD.
- To evaluate the effectiveness of interferon-alpha treatment in HGV-seropositive patients, particularly those with co-infections.
Main Methods:
- Analysis of 202 patients with CHD for markers of HBV, HCV, HGV, and TTV infections.
- Liver biopsy was performed on a subset of patients.
- Interferon-alpha treatment efficacy was assessed in patients with HGV and HBV/HCV co-infections.
Main Results:
- HGV RNA and TTV DNA were detected in 19.8% and 11.8% of patients, respectively.
- Biochemical and morphological changes in patients with HGV and TTV monoinfections indicated a potential role in liver disease.
- Two out of seven patients with HGV + HBV/HCV co-infections showed a positive response to interferon-alpha treatment after 3 months.
Conclusions:
- The precise contribution of HGV and TTV to the pathogenesis of chronic hepatic diseases remains uncertain.
- Further research is essential for the detection and comprehensive examination of patients infected with HGV and TTV.
- Therapeutic strategies should consider the presence of HGV RNA, TTV DNA, viral genome in hepatocytes, and histological liver changes.
Aim:
To examine clinical, immunological and morphological features of HGV- and TTV-infections in patients with chronic hepatic diseases (CHD) and assess efficiency of treatment of HGV-seropositive patients.
Material And Methods:
202 patients with CHD were examined for markers of HBV-, HCV-, HGV- and TTV-infections. Some patients were subjected to puncture biopsy of the liver. Efficiency of interferon-alpha treatment of HGV and HBV/HCV coinfection was studied.
Results:
HGV RNA and TTV DNA were detected in 19.8 and 11.8% of cases, respectively. Biochemical indices in patients with HGV and TTV monoinfections significantly differed from those in the control group while morphological changes in most of them corresponded to those with hepatitis. INF-alpha was given to 7 patients with HGV + HBV/HCV infections. A response was achieved in 3 months in 2 of them.
Conclusion:
The role of HGV and TTV in hepatic diseases pathology is still unclear. Further studies on detection and examination of patients infected with G and TT viruses are necessary. When choosing therapy, the presence of HGV RNA and TTV DNA in blood serum, virus genome in hepatocytes and histological changes in hepatic tissue should be considered.
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