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Chronic, Acute, and Reactivated HIV Infection in Humanized Immunodeficient Mouse Models
Published on: December 3, 2019
Childhood HIV-associated nephropathy: 36 years later
Patricio E Ray1,2, Jinliang Li3,4, Jharna R Das3,4
1Department of Pediatrics, Child Health Research Center, University of Virginia School of Medicine, Room 2120, MR4 Building, 409 Lane Road, Charlottesville, VA, 22908, USA. Pray@virginia.edu.
HIV-associated nephropathy (HIVAN) in children is a serious kidney disease linked to HIV infection and certain genetic factors. Advances in treatment offer hope, but better prevention and management strategies are crucial for affected children worldwide.
Area of Science:
- Nephrology
- Infectious Diseases
- Genetics
Background:
- HIV-associated nephropathy (HIVAN) primarily impacts individuals of African ancestry with HIV, particularly those without effective antiretroviral therapy (ART).
- Childhood HIVAN presents with significant proteinuria, impaired kidney function, and characteristic histological changes including glomerulosclerosis and tubular dilatation.
- Pathogenesis involves inflammatory cell infiltration, kidney epithelial cell infection, and contributions from viral (e.g., HIV-Tat gene) and genetic factors (e.g., APOL1 risk variants).
Purpose of the Study:
- To review recent advancements in understanding the pathogenesis and treatment of childhood HIVAN over the past decade.
- To highlight the mechanisms of kidney epithelial cell infection and the roles of cytokines, HIV-Tat, and APOL1 gene variants.
Main Methods:
- Literature review focusing on studies published within the last 10 years.
- Analysis of research on HIVAN pathogenesis, including viral and genetic factors.
- Examination of treatment strategies and outcomes for childhood HIVAN.
Main Results:
- Modern ART has reduced the incidence and improved outcomes of childhood HIVAN.
- Despite ART improvements, challenges remain in chronic treatment adherence for pediatric populations.
- Key pathogenic mechanisms include inflammatory responses, epithelial cell susceptibility, and genetic predispositions like APOL1 variants.
Conclusions:
- Understanding the complex interplay of viral, genetic, and inflammatory factors is critical for managing childhood HIVAN.
- Enhanced prevention and treatment programs are essential to combat HIVAN in children living with HIV.
- Further research is needed to optimize long-term ART adherence and develop targeted therapies for HIVAN.
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