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Updated: May 25, 2026

Development of an IFN-γ ELISpot Assay to Assess Varicella-Zoster Virus-specific Cell-mediated Immunity Following Umbilical Cord Blood Transplantation
Published on: July 9, 2014
Non-viral infections in children after renal transplantation
Francesca Mencarelli1, Stephen D Marks
1Department of Paediatric Nephrology, Great Ormond Street Hospital for Children NHS Trust, Great Ormond Street, London, WC1N 3JH, England, UK.
Insights
Non-viral infections are a serious risk for pediatric kidney transplant recipients (RTR). This review examines infection risks, prevention, and treatment to improve patient outcomes and allograft survival.
Area of Science:
- Pediatric Nephrology
- Transplant Immunology
- Infectious Diseases
Background:
- Renal transplantation is the optimal treatment for pediatric end-stage renal failure.
- Advances in immunosuppression and surgical techniques have improved patient and graft survival.
- Non-viral infections remain a significant complication for pediatric renal transplant recipients (RTR).
Purpose of the Study:
- To review the incidence, timing, risk factors, prevention, and treatment of non-viral infections in pediatric RTR.
- To critically evaluate current immunosuppressive regimens and their risk-benefit ratio.
- To optimize renal allograft survival while minimizing infectious complications.
Main Methods:
- Literature review of non-viral infections in pediatric renal transplant recipients.
- Analysis of risk factors including immunization status, pathogen exposure, and immunosuppression levels.
- Evaluation of infection sources: donor-derived, transplant fluids, catheters, and stents.
- Review of urinary tract infection prevalence in patients with lower urinary tract dysfunction.
Main Results:
- High immunosuppression burden in the first 6 months post-transplant increases the risk of life-threatening infections, including Cytomegalovirus.
- Bacterial infections can originate from various sources related to the transplant procedure and devices.
- Urinary tract infections are common and can lead to renal allograft damage, especially in patients with lower urinary tract dysfunction.
Conclusions:
- Optimizing immunosuppressive regimens is crucial for balancing rejection prevention and infection risk in pediatric RTR.
- Proactive management of infection risks, including appropriate prophylaxis and monitoring, is essential.
- Further research into risk stratification and targeted prevention strategies can improve long-term outcomes for pediatric kidney transplant recipients.
Abstract:
Renal transplantation has long been recognised as the gold standard treatment for children with end-stage renal failure. There has been an improvement over the years in patient and renal allograft survival because of improved immunosuppression, surgical techniques and living kidney donation. Despite reduced acute allograft rejection rates, non-viral infections continue to be a serious complication for paediatric renal transplant recipients (RTR). The risk of infections in RTR is determined by the pre-transplantation immunisation status, post-transplant exposure to potential pathogens and the amount of immunosuppression. The greatest risk of life-threatening and Cytomegalovirus infections is during the first 6 months post-transplant owing to a high immunosuppressive burden. The potential sources of bacterial infections are donor derived, transplant medium fluid, peritoneal and haemodialysis catheter and transplant ureteric stent. Urinary tract infections are frequent in patients with lower urinary tract dysfunction and can result in renal allograft damage. This review outlines the incidence, timing, risk factors, prevention and treatment of non-viral infections in paediatric RTR by critically reviewing current immunosuppressive regimens, their risk-benefit ratio in order to optimise renal allograft survival with reduced rates of rejection and infectious complications.
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