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Updated: May 11, 2026

Generation of Multivirus-specific T Cells to Prevent/treat Viral Infections after Allogeneic Hematopoietic Stem Cell Transplant
Published on: May 27, 2011
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.
Abstract:
Among the immunocompetent, infections with parvovirus B19 (B19V) and human bocavirus (HBoV) 1 range clinically from asymptomatic to severe, while following allogeneic hematopoietic SCT (HSCT) B19V can cause a persistent severe illness. The epidemiology and clinical impact of HBoV1 and the other emerging parvovirus 4 (PARV4) among immunocompromised patients have not been established. To determine the occurrence and clinical spectrum of B19V, PARV4 and HBoV1 infections, we performed a longitudinal molecular surveillance among 53 allogeneic HSCT recipients for pre- and post-HSCT DNAemias of these parvoviruses. Quantitative real-time PCR showed B19V DNA in sera of 16 (30%) patients, at mean levels of 4.6 × 10(3), 9.9 × 10(7), 1.1 × 10(10) and 1.6 × 10(2) B19V DNA copies/mL pre-HSCT (9/53), and at 1 (6/53), 2 (4/53) and 3 months (1/25) post HSCT, respectively. However, no clinical manifestation correlated with the presence of B19V viremia. All B19V sequences were of genotype 1. None of the sera investigated contained PARV4 or HBoV1 DNAs. Our data demonstrate B19V viremia to be frequent among pediatric allogeneic HSCT recipients, yet without apparent clinical correlates. PARV4 or HBoV1 viremias were not seen in these immunocompromised patients.
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