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Updated: Nov 18, 2025

An Efficient and Simple Method to Establish NK and T Cell Lines from Patients with Chronic Active Epstein-Barr Virus Infection
Published on: March 30, 2018
Concomitant nephrotic syndrome and tubulointerstitial nephritis in a child with Epstein-Barr virus mononucleosis
Ratna Acharya1, Xu Zeng2, Kiran Upadhyay3
1Pediatrics, University of Florida, Gainesville, Florida, USA.
Abstract:
Acute kidney injury (AKI) and nephrotic syndrome (NS) are uncommon manifestations of Epstein-Barr virus (EBV) mononucleosis. We report a 4-year-old boy with Infectious mononucleosis (IM) who presented with dialysis-requiring AKI and NS. Renal biopsy showed severe acute tubular necrosis, mild chronic interstitial nephritis and focal podocyte foot processes effacement. EBV early RNA was not detected in the renal tissue. However, immunophenotyping of peripheral lymphocytes showed increased cytotoxic T cell activity and increased memory B cells. Treatment with steroid led to rapid resolution of NS within 3 weeks. Renal function stabilised. EBV viral capsid antigen (VCA) IgM remained elevated until 4 months before starting to decline when VCA IgG and nuclear antigen started appearing. B lymphocytes are the predominant target cells in EBV infection and additionally may also act as antigen presenting cells to T lymphocytes, thereby eliciting the strong immune response and leading to podocyte and tubulointerstitial injury.
Insights
Epstein-Barr virus (EBV) can cause rare kidney problems like acute kidney injury (AKI) and nephrotic syndrome (NS) in children. Steroid treatment helped a young boy recover from EBV-related kidney complications.
Area of Science:
- Pediatric Nephrology
- Infectious Diseases
- Immunology
Background:
- Infectious mononucleosis (IM), typically caused by Epstein-Barr virus (EBV), is common in adolescents and young adults.
- While IM primarily affects B lymphocytes, its association with severe renal manifestations like acute kidney injury (AKI) and nephrotic syndrome (NS) is infrequent.
Observation:
- A 4-year-old boy presented with severe AKI requiring dialysis and NS during IM.
- Renal biopsy revealed acute tubular necrosis and podocyte injury, but EBV early RNA was undetectable in kidney tissue.
- Peripheral lymphocyte analysis indicated heightened cytotoxic T cell activity and an increase in memory B cells.
Findings:
- Steroid therapy resulted in rapid resolution of NS within three weeks, with stabilization of renal function.
- Serological markers confirmed a primary EBV infection, with a characteristic pattern of antibody development over four months.
- The study suggests that EBV-induced immune responses, involving B and T lymphocytes, may contribute to kidney damage.
Implications:
- This case highlights EBV as a potential cause of severe renal disease in children, necessitating prompt diagnosis and management.
- Understanding the immunopathogenesis of EBV-related kidney injury can inform treatment strategies for similar cases.
- Further research into the role of lymphocyte subsets in EBV-associated nephropathies is warranted.
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