Cytomegalovirus infection in the first year after pediatric kidney transplantation

Corentin Tanné1, Pascal Roy2, Émilie Frobert3

  • 1Centre de référence des maladies rénales rares, service de néphrologie, rhumatologie dermatologie pédiatriques, hospices civils de Lyon, 69003 Lyon, France; Université Claude-Bernard Lyon 1, 69000 Lyon, France.

Nephrologie & Therapeutique
|June 12, 2018
PubMed

Insights

Cytomegalovirus (CMV) infection affects 27.9% of pediatric kidney transplant recipients within the first year. Donor/recipient CMV status significantly influences infection risk, underscoring the need for vigilant monitoring, especially in intermediate-risk patients.

Area of Science:

  • Pediatric Nephrology
  • Transplant Immunology
  • Virology

Background:

  • Cytomegalovirus (CMV) is prevalent in adult transplant recipients (40-90%).
  • Pediatric kidney transplant recipients are susceptible to primary CMV infection or reactivation due to immunosuppression.
  • The incidence of CMV infection in this population remains understudied.

Purpose of the Study:

  • To determine the incidence and timing of CMV infection in the first year post-kidney transplantation in children.
  • To analyze CMV infection rates based on donor (D) and recipient (R) CMV serostatus (high-risk D+/R-, intermediate-risk R+, low-risk D-/R-).

Main Methods:

  • Retrospective cohort study of 136 pediatric kidney transplant recipients (2003-2014).
  • Patients categorized into high, intermediate, and low CMV risk groups based on serostatus.
  • CMV infection defined as asymptomatic viral replication; CMV disease as symptomatic replication.
  • Oral valganciclovir prophylaxis administered to high-risk recipients.

Main Results:

  • Overall, 38 patients (27.9%) developed CMV infection within the first year.
  • Incidence was highest in high-risk (40.6%) and intermediate-risk (45.3%) groups.
  • Ten infected patients developed tissue-invasive CMV disease.

Conclusions:

  • CMV infection occurs in 27.9% of pediatric kidney transplant recipients during the first year.
  • Donor and recipient CMV serostatus are critical determinants of infection risk.
  • Enhanced surveillance is crucial for intermediate-risk patients to prevent severe outcomes.

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