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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
COVID-19 mRNA Vaccine Tolerance and Immunogenicity in Hematopoietic Stem Cell Transplantation Recipients Aged 5-11
Agnieszka Matkowska-Kocjan1, Joanna Owoc-Lempach2, Kamila Ludwikowska1
1Department and Clinic of Pediatric Infectious Diseases, Wroclaw Medical University, 50-368 Wrocław, Poland.
Insights
The Pfizer-BioNTech COVID-19 vaccine is safe and effective in children aged 5-11 after stem cell transplants. Immunocompromised children may need additional vaccine doses for optimal protection.
Area of Science:
- Pediatric Hematology/Oncology
- Infectious Diseases
- Vaccinology
Background:
- The COVID-19 pandemic highlighted the need for effective vaccines.
- Limited data exist on vaccine efficacy in immunocompromised pediatric populations, specifically after allogeneic hematopoietic stem cell transplantation (allo-HSCT).
Purpose of the Study:
- To assess the safety and immunogenicity of the mRNA BNT162b2 (Pfizer/BioNTech) COVID-19 vaccine in children aged 5-11 who have undergone allo-HSCT.
- To compare vaccine response in allo-HSCT recipients with healthy children.
Main Methods:
- A prospective study involving two cohorts: 34 children post-allo-HSCT and 35 healthy children aged 5-11.
- Vaccination with two doses of mRNA BNT162b2 (10 µg).
- Adverse events monitored via electronic surveys; immunogenicity assessed by anti-SARS-CoV-2 IgG titers.
Main Results:
- All reported adverse events were mild, with injection site pain being most common.
- Anti-SARS-CoV-2 IgG production was similar between allo-HSCT recipients and healthy children.
- Children post-allo-HSCT on immunosuppressive therapy showed a weaker immune response compared to those off treatment.
Conclusions:
- The mRNA BNT162b2 vaccine is well-tolerated and immunogenic in children aged 5-11 post-allo-HSCT.
- Children off immunosuppressive treatment demonstrated excellent antibody production.
- Children on immunosuppression may benefit from an intensified vaccination schedule.
Abstract:
The SARS-CoV-2 pandemic had a devastating impact on the world’s population in the years 2020−2022. The rapid development of vaccines enabled a reduction in the mortality and morbidity of COVID-19, but there are limited data about their effects on immunocompromised children. The aim of this prospective study was to evaluate the safety and efficacy of the mRNA BNT162b2 (Pfizer/Biontech) vaccine in allogeneic hematopoietic stem cell transplantation (allo-HSCT) recipients. Material and methods: Two cohorts of 34 children after allo-HSCT and 35 healthy children aged 5−11 years were vaccinated with two doses of the mRNA BNT162b2 (10 µg) vaccine. All children were evaluated for adverse effects with electronic surveys and the immunogenicity of the vaccine was assessed with anti-SARS-CoV-2 IgG titer measurements. Results: All reported adverse events (AEs) were classified as mild. The most common AE was pain at the injection site. All the other AEs (both local and systemic) were rarely reported (<15% patients). Both groups showed a similar response in anti-SARS-CoV-2 IgG production. Patients after allo-HSCT that were undergoing immunosuppressive treatment presented a poorer immunological response than patients off of treatment. Time since HSCT, patient age, lymphocyte count, and total IgG concentration did not correlate with initial/post-vaccination anti-SARS-CoV-2 IgG titers. Most patients who were eligible for a third dose of the vaccine had an excellent humoral response observed after two vaccine doses. Conclusions: The COVID-19 mRNA BNT162b2 vaccine is very well tolerated and highly immunogenic in 5−11-year-old children after HSCT. Children >2 years of age after HSCT who did not receive immunosuppressive treatment presented excellent antibody production after two doses of the vaccine, but children on immunosuppression may require a more intense vaccination schedule.
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