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Published on: October 17, 2018
Does Zika virus infection induce prolonged remissions in children with idiopathic nephrotic syndrome?
Carolina Peralta-Aros1, Víctor García-Nieto2
1Hospital Uyapar, Puerto Ordaz, Venezuela. carolinaperalt@gmail.com.
Insights
Zika virus (ZIKV) infection may induce remission in pediatric nephrotic syndrome. Two children with this condition experienced complete disease remission following ZIKV infection, suggesting a potential therapeutic link.
Area of Science:
- Virology
- Pediatric Nephrology
- Immunology
Background:
- Idiopathic nephrotic syndrome (INS) is a significant kidney disorder in children.
- Zika virus (ZIKV), a mosquito-borne flavivirus, has emerged as a global health concern.
- The potential impact of ZIKV infection on immune-mediated diseases remains under investigation.
Observation:
- Two pediatric cases of INS are presented: one steroid-dependent and one steroid-resistant.
- Both patients were diagnosed with concurrent ZIKV infection.
- Clinical data revealed significant improvements in nephrotic syndrome following ZIKV infection.
Findings:
- The first patient, a 2.5-year-old girl, achieved complete remission of steroid-dependent INS after ZIKV infection, allowing for steroid withdrawal.
- The second patient, a 7-year-old boy with steroid-resistant INS, experienced a gradual decline in proteinuria post-ZIKV infection, leading to complete remission over 12 months.
- These cases suggest a possible correlation between ZIKV infection and remission of pediatric nephrotic syndrome.
Implications:
- The findings suggest a potential immunomodulatory role for ZIKV infection in pediatric nephrotic syndrome.
- Further research is warranted to explore the mechanisms underlying ZIKV's effect on the immune system and its therapeutic potential.
- This observation may open new avenues for understanding and managing nephrotic syndrome in children.
Background:
Zika is an emerging mosquito-borne flavivirus. We report two pediatric patients diagnosed with idiopathic nephrotic syndrome who achieved complete remission of the disease after suffering Zika virus (ZIKV) infection.
Case Diagnosis/Treatment:
The first patient was a young girl aged 2.5 years with steroid-dependent nephrotic syndrome who was subsequently diagnosed with ZIKV infection. Following the infection, the steroid dose could be reduced until complete withdrawal. The patient persists in complete remission. The second patient was a steroid-resistant boy aged 7 years who was scheduled for a renal biopsy when he was diagnosed with ZIKV infection. A week after the recovery phase of the acute rash, proteinuria was noted to be gradually falling. Today, 12 months later, he is in complete remission of the disease.
Conclusions:
We are aware that the improvement observed in our two patients after ZIKV infection may be be random. However, it is also possible that future studies will discover that ZIKV infection has some effect on the cellular immune system similar to that of measles infection.
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