Related Experiment Video
Updated: Aug 13, 2025

Generation of Multivirus-specific T Cells to Prevent/treat Viral Infections after Allogeneic Hematopoietic Stem Cell Transplant
Published on: May 27, 2011
Human Mastadenovirus A Infection in a Child During the Course of Hematopoietic Stem Cell Transplant
Siddika Songul Yalcin1, B Baris Kuskonmaz, Vicente Perez-Brocal
1From the Department of Social Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Abstract:
Following primary infection, human mastadenoviruses can persist in various tissues. We report a case of a pediatric patient with Fanconi anemia who had a complicated posttransplant course after allogeneic hematopoietic stem cell transplant that was associated with human mastadenovirus infection. Human mastadenovirus reactivation was detected with metagenomic analysis during a 3-month followup period; the predominant rate of occurrence of human mastadenoviruses was 1.1% on day 0, 84% on day +15, 90% on day +30, and 42% on day +82. Virus shedding continued up to 3 months after transplant. At 36 months after hematopoietic stem celltransplant, the patient was in good clinical condition with full donor chimerism. Long-term follow-up studies for human mastadenoviruses are needed to determine latency period.
Insights
Human mastadenovirus reactivation can complicate recovery after allogeneic hematopoietic stem cell transplant in pediatric patients. Continued monitoring is crucial for understanding virus persistence and latency post-transplant.
Area of Science:
- Virology
- Immunology
- Hematology
Background:
- Human mastadenoviruses are known to persist in various tissues post-primary infection.
- Allogeneic hematopoietic stem cell transplantation (HSCT) is a complex procedure with potential complications.
- Pediatric patients with Fanconi anemia are particularly vulnerable post-HSCT.
Observation:
- A pediatric patient with Fanconi anemia experienced a complicated post-HSCT course.
- Metagenomic analysis revealed human mastadenovirus reactivation during the 3-month follow-up period.
- High viral loads were detected at day +15 (84%) and day +30 (90%), with shedding continuing for 3 months.
Findings:
- Human mastadenovirus reactivation occurred in a pediatric HSCT recipient.
- The virus demonstrated significant replication and shedding in the post-transplant period.
- The patient achieved full donor chimerism and good clinical condition at 36 months post-HSCT.
Implications:
- This case highlights the importance of monitoring for human mastadenovirus reactivation in HSCT recipients.
- Further long-term follow-up studies are necessary to elucidate the latency patterns of human mastadenoviruses.
- Understanding viral persistence is key to improving outcomes for immunocompromised patients.
More Related Videos
Related Concept Videos
Bone Marrow Sampling and Transplants
The transplant begins with high doses of chemotherapy and radiation treatment, which aim to destroy...
Immunodeficiency Diseases
There are three main causes of immunodeficiency...

