Human parvoviruses B19, PARV4 and bocavirus in pediatric patients with allogeneic hematopoietic SCT

J Rahiala1, M Koskenvuo, P Norja

  • 11] Division of Pediatric Hematology, Oncology and Stem Cell Transplantation, Children's Hospital, Helsinki University Central Hospital and University of Helsinki, Helsinki, Finland [2] Department of Pediatrics, Porvoo Hospital, Porvoo, Finland.

Insights

Parvovirus B19 (B19V) viremia is common in pediatric hematopoietic stem cell transplant (HSCT) patients but shows no clear clinical impact. Other parvoviruses, PARV4 and HBoV1, were not detected in this immunocompromised group.

Area of Science:

  • Virology
  • Immunology
  • Pediatrics

Background:

  • Parvovirus B19 (B19V) can cause severe illness post-hematopoietic stem cell transplant (HSCT).
  • The impact of human bocavirus 1 (HBoV1) and parvovirus 4 (PARV4) in immunocompromised individuals remains unclear.
  • Understanding parvovirus epidemiology in HSCT recipients is crucial for managing immunocompromised patients.

Purpose of the Study:

  • To investigate the occurrence and clinical spectrum of B19V, PARV4, and HBoV1 infections in pediatric HSCT recipients.
  • To determine the frequency and viral load of parvovirus DNAemias before and after HSCT.
  • To assess the clinical manifestations associated with these parvovirus infections post-transplant.

Main Methods:

  • Longitudinal molecular surveillance of 53 pediatric allogeneic HSCT recipients.
  • Quantitative real-time PCR assays for B19V, PARV4, and HBoV1 DNA in serum samples.
  • Pre- and post-HSCT sample collection for DNAemia analysis.

Main Results:

  • B19V DNA was detected in 30% of patients, with varying viral loads pre- and post-HSCT.
  • No clinical manifestations were correlated with the presence of B19V viremia.
  • PARV4 and HBoV1 DNA were not detected in any of the investigated serum samples.

Conclusions:

  • B19V viremia is frequent in pediatric allogeneic HSCT recipients but appears to have no significant clinical impact.
  • PARV4 and HBoV1 infections were not observed in this cohort of immunocompromised patients.
  • Further research may be needed to understand the long-term implications of B19V viremia in HSCT survivors.

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