Related Experiment Video
Updated: Apr 1, 2026

Modeling Hepatitis B Virus Infection in Non-Hepatic 293T-NE-3NRs Cells
Published on: June 5, 2020
[Management of hepatitis B virus and hepatitis C virus infection in chronic kidney failure]
Anaïs Vallet-Pichard1, Stanislas Pol1
1Unité d'hépatologie, hôpital Cochin, AP-HP, 27, rue du Faubourg-Saint-Jacques, 75014 Paris, France; Inserm U 1016, 27, rue du Faubourg-Saint-Jacques, 75014 Paris, France; Université Paris-Descartes, 27, rue du Faubourg-Saint-Jacques, 75014 Paris, France.
Insights
Screening for hepatitis B (HBV) and C (HCV) is crucial for dialysis and kidney transplant patients. Early diagnosis and new antiviral treatments improve outcomes, while vaccination and hygiene prevent infections.
Area of Science:
- Nephrology
- Hepatology
- Infectious Diseases
Background:
- Chronic hepatitis B (HBV) and C (HCV) infections pose significant diagnostic and therapeutic challenges in dialysis and kidney transplant recipients.
- Nosocomial exposure, including blood transfusions, contributes to the high prevalence of HBV and HCV in this vulnerable population.
- These chronic infections negatively impact patient and allograft survival and increase the risk of de novo glomerulonephritis.
Purpose of the Study:
- To highlight the importance of screening for HBV and HCV markers in all dialysis patients, regardless of transplantation candidacy.
- To discuss the evaluation of liver disease severity using liver biopsy and the limitations of noninvasive markers in renal patients.
- To review current and emerging therapeutic strategies for HBV and HCV in kidney disease patients.
Main Methods:
- Review of diagnostic and therapeutic guidelines for HBV and HCV in dialysis and kidney transplant patients.
- Discussion of the role of liver biopsy in assessing liver disease severity and guiding antiviral therapy.
- Analysis of treatment outcomes with direct-acting antivirals for HCV and nucleos(t)tidic analogues for HBV.
Main Results:
- HCV treatment has shifted to potent and well-tolerated oral direct-acting antivirals, overcoming limitations of previous interferon-based therapies.
- Second-generation nucleos(t)tidic analogues (entecavir, tenofovir) effectively suppress HBV replication and are recommended for dialysis patients with significant fibrosis and transplant candidates.
- Liver biopsy remains essential for accurate fibrosis staging in renal patients, as noninvasive markers show reduced accuracy.
Conclusions:
- Mandatory screening for HBV and HCV markers is essential for all dialysis patients.
- Timely and appropriate antiviral therapy, alongside preventive measures like vaccination and hygiene, can significantly improve outcomes for HBV and HCV-infected kidney disease patients.
- Careful patient selection and management are crucial for successful renal transplantation in patients with or at risk of viral hepatitis.
Abstract:
Chronic infections by hepatitis B (HBV) and C virus (HCV) result in diagnosis and therapeutic issues in dialysis and kidney recipients patients. The exposure to nosocomial, including blood transfusion, risk explains the high prevalence of HBV and HCV infection in this setting. Chronic infection reduces the survival of both patients and allografts, including a specific risk of de novo glomerulonephritis. Cirrhosis was considered as a contra-indication to renal transplantation given the high risk of decompensation and death, questionning the indication of a combined liver and kidney transplantation. Thus, it is mandatory to screen HBV and HCV markers in all dialysis patients, whether or not they are candidates to transplantation. Liver biopsy allows evaluating the severity of the liver disease since the noninvasive markers of fibrosis appear to be less accurate in "renal" patients than in the general population and to better define antiviral therapeutic indications. HCV treatment was mainly based on pegylated interferon α (and low doses of ribavirin), which is contra-indicated in kidney recipients given the risk of graft rejection; HCV treatment is now based on the use of oral direct acting antivirals, which are very potent and well tolerated. HBV replication is now easily suppressed by second-generation nucleos(t)tidic analogues (entecavir and tenofovir), which will be indicated in all the dialysis patients with significant fibrosis (F2,3 or 4 according to the Metavir scoring system) and in any candidate to renal transplantation and to any HBsAg-positive kidney recipients. The best treatment remains preventive by anti-HBV vaccination for HBV and by the respect of universal hygiene rules for HCV.
More Related Videos
10:25"Liver-on-a-Chip" Cultures of Primary Hepatocytes and Kupffer Cells for Hepatitis B Virus Infection
Published on: February 19, 2019
11:34A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target
Published on: May 10, 2022
Related Concept Videos
Hepatitis
Chronic Kidney Disease III: Interprofessional Care
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow
Chronic Kidney Disease IV: Nursing Management
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test
Chronic Kidney Disease I: Introduction