Related Experiment Video
Updated: Apr 4, 2026

Establishment of the Dual Humanized TK-NOG Mouse Model for HIV-associated Liver Pathogenesis
Published on: September 11, 2019
Immunologic Predictors of Liver Transplantation Outcomes in HIV-HCV Co-Infected Persons
Ashwin Balagopal1, Burc Barin2, Jeffrey Quinn1
1Department of Medicine, Johns Hopkins University, Baltimore, MD, 21205, United States of America.
Insights
Predicting liver transplant outcomes in HIV-HCV co-infected patients is crucial. Pre-transplant monocyte activation markers like sCD14 and IL-10 may predict graft loss and rejection, respectively, in these high-risk individuals.
Area of Science:
- Immunology
- Hepatology
- Infectious Diseases
Background:
- Liver disease is a major cause of death in HIV-infected individuals, even with treatment.
- Hepatitis C Virus (HCV) co-infection is common in HIV patients and leads to poorer outcomes, often necessitating liver transplantation (LT).
- Post-LT outcomes remain suboptimal for patients with HIV-HCV co-infection.
Purpose of the Study:
- To identify pre-transplant immunologic biomarkers that predict outcomes after liver transplantation in HIV-HCV co-infected individuals.
- To investigate the association between immune activation, microbial translocation, and Th1/Th2 skewing with graft loss, rejection, and recurrent HCV post-LT.
Main Methods:
- A cohort of 69 HIV-HCV co-infected patients undergoing LT was studied.
- Pre-transplant immunologic biomarkers (sCD14, IL-10) were measured.
- Cox-proportional hazards models were used to analyze predictors of post-LT outcomes, including graft loss, rejection, and recurrent HCV.
Main Results:
- Lower pre-LT sCD14 levels were associated with increased risk of graft loss (HR 0.10).
- Higher pre-LT IL-10 levels were linked to a greater risk of acute rejection (HR 2.10).
- No specific biomarkers predicted severe recurrent HCV post-LT.
Conclusions:
- Pre-transplant monocyte activation, indicated by sCD14 and IL-10 levels, may be mechanistically linked to graft health and rejection risk in HIV-HCV co-infected patients undergoing liver transplantation.
- These biomarkers could potentially aid in risk stratification and management strategies for this vulnerable patient population.
Abstract:
Liver disease is a leading cause of mortality among HIV-infected persons in the highly active anti-retroviral therapy (HAART) era. Hepatitis C Virus (HCV) co-infection is prevalent in, and worsened by HIV; consequently many co-infected persons require liver transplantation (LT). Despite the need, post-LT outcomes are poor in co-infection. We examined predictors of outcomes post-LT. Immunologic biomarkers of immune activation, microbial translocation, and Th1/Th2 skewing were measured pre-LT in participants enrolled in a cohort of HIV infected persons requiring solid organ transplant (HIVTR). Predictive biomarkers were analyzed in Cox-proportional hazards models; multivariate models included known predictors of outcome and biomarkers from univariate analyses. Sixty-nine HIV-HCV co-infected persons with available pre-LT samples were tested: median (IQR) CD4+ T-cell count was 286 (210-429) cells mm-3; 6 (9%) had detectable HIV RNA. Median (IQR) follow-up was 2.1 (0.7-4.0) years, 29 (42%) people died, 35 (51%) had graft loss, 22 (32%) were treated for acute rejection, and 14 (20%) had severe recurrent HCV. In multivariate models, sCD14 levels were significantly lower in persons with graft loss post-LT (HR 0.10 [95%CI 0.02-0.68]). IL-10 levels were higher in persons with rejection (HR 2.10 [95%CI 1.01-4.34]). No markers predicted severe recurrent HCV. Monocyte activation pre-LT may be mechanistically linked to graft health in HIV-HCV co-infection.
More Related Videos
Related Concept Videos
Tissue Transplantation
The Biology of Tissue Transplantation
The biology of tissue transplantation hinges on the Major Histocompatibility Complex (MHC) molecules. These molecules...
Cell-mediated Immune Responses
Pulmonary Tuberculosis I
Causative Organism
The primary infectious agent causing tuberculosis is Mycobacterium tuberculosis, a slow-growing, acid-fast, aerobic rod that exhibits sensitivity to heat and ultraviolet light. Instances of Mycobacterium bovis and Mycobacterium avium contributing to the development of TB infection are rare.
Mode of...

