Cytomegalovirus (CMV) infections in children undergoing hematopoetic stem cell transplantation

Agnieszka Zaucha-Prazmo1, Beata Wójcik, Katarzyna Drabko

  • 1Department of Pediatric Haematology and Oncology, Medical University, 20-930 Lublin, Poland.

Insights

Cytomegalovirus (CMV) infection is a significant risk after hematopoetic stem cell transplantation (HSCT) in children. Key risk factors include transplant type, recipient CMV seropositivity, and graft-versus-host disease (GvHD).

Area of Science:

  • Hematology
  • Infectious Diseases
  • Transplantation Immunology

Background:

  • Cytomegalovirus (CMV) infection poses a major threat to patient outcomes following hematopoetic stem cell transplantation (HSCT).
  • Understanding risk factors is crucial for preventing CMV disease and improving survival rates in pediatric HSCT recipients.

Purpose of the Study:

  • To identify and analyze the risk factors associated with Cytomegalovirus (CMV) disease development in pediatric patients undergoing HSCT.

Main Methods:

  • Retrospective analysis of 110 pediatric patients who underwent HSCT.
  • Monitoring for CMV antigenemia (CMV infection in white blood cells).
  • Evaluation of CMV serological status (donor and recipient), transplant type, graft-versus-host disease (GvHD), and timing of CMV infection.

Main Results:

  • CMV antigenemia was diagnosed in 14.5% (16/110) of pediatric HSCT patients.
  • Most CMV infections occurred after allogeneic HSCT (alloHSCT), with one case post-autologous HSCT.
  • Risk factors identified include the type of transplant, pre-transplant CMV seropositivity in the recipient, and the presence/intensity of GvHD.
  • CMV reactivation was the primary mode of infection, occurring early post-transplant in most cases, but late-onset infections and second reactivations were also observed.

Conclusions:

  • CMV infection remains a significant complication post-pediatric HSCT.
  • Transplant type, recipient serostatus, and GvHD are critical risk factors for CMV disease.
  • CMV reactivation is common, and infection can manifest even in the late post-transplant period, including after autologous HSCT.

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