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Updated: Aug 30, 2026

Establishment of the Dual Humanized TK-NOG Mouse Model for HIV-associated Liver Pathogenesis
Published on: September 11, 2019
[Liver transplantation: is it possible in HIV/HCV co-infected patients?]
D Vittecoq1, E Teicher, M Merad
1Service des maladies infectieuses, hôpital Paul-Brousse, 12-14, avenue Paul-Vaillant-Couturier, 94800 Villejuif, France. daniel.vittecoq@pbr.ap-hop-paris.fr
Insights
Liver transplantation in patients with HIV and HCV co-infection is feasible with strict selection criteria. This approach, while experimental, requires careful management and a multidisciplinary team for successful outcomes.
Area of Science:
- Hepatology
- Infectious Diseases
- Transplantation Medicine
Background:
- Hepatitis C virus (HCV) co-infection significantly increases morbidity and mortality in patients with human immunodeficiency virus (HIV).
- Liver transplantation is typically contraindicated in HIV-HCV co-infected patients due to concerns about immunodeficiency, co-infection, and ethical considerations.
Purpose of the Study:
- To evaluate the feasibility of liver transplantation in patients co-infected with HIV and HCV.
- To assess the outcomes and complications associated with liver transplantation in this specific patient population.
Main Methods:
- A cohort of seven HIV-HCV co-infected patients underwent liver transplantation between December 1999 and March 2002.
- Patients were selected based on strict criteria, including adequate CD4 counts and undetectable viral loads, and received optimized antiretroviral therapy.
- Follow-up averaged 14 months, with monitoring for opportunistic infections, viral loads, and post-transplant complications.
Main Results:
- One patient died within 3 months post-transplantation; another experienced esophageal candidiasis.
- HCV recurrence was observed in all patients, with four undergoing interferon/ribavirin therapy.
- Common complications included transient renal insufficiency, diabetes, pancreatitis, and mitochondrial chain abnormalities. Highly active antiretroviral therapy (HAART) required modifications due to toxicity or virologic failure.
Conclusions:
- Liver transplantation in carefully selected HIV-HCV co-infected patients appears feasible.
- This experimental strategy necessitates stringent patient selection and a collaborative, multidisciplinary approach to manage complex post-transplant care.
Abstract:
The prognosis of HIV infection has been modified by antiretroviral therapy. However, the morbidity and the mortality of HCV co-infection increase and may be a major problem of health service. Up to now co-infected patients are excluded of transplantation due to complexity, the ethical aspects, the immunodeficiency and the co-infection. This study tries to estimate the feasibility in this population. Between December 1999 and March 2002, seven patients were transplanted. The average of CD4 was 332/ml; the viral load was <50 copies/ml. Before transplantation, no patient had experienced opportunist infection and all patients received antiretroviral therapy adapted to their history. The average follow-up is of 14 months: one patient died 3 months after transplantation, the other one presented a candida in oesophagus, the average of CD4 was 280/ml, and viral load was <50 copies/ml in five patients. A relapse of HVC was observed in all patients. Interferon/rivabirine therapy was proposed for four patients. Every patient received tacrolimus and corticoids. HAART were modified four times for toxicity and one time for virological failure. We observed two cases of transient renal insufficiency, two cases of diabetes, two cases of pancreatitis, and abnormalities of the respiratory mitochondrial chain in four patients. Finally, liver transplantation in HIV-HCV co-infected patients seems to be feasible when strict criteria of selection are taken into account. This still experimental strategy requires a multidisciplinary partnership.
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