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DOI 10.1007/s00432-026-06632-4

Медицинская библиотека · Journal of cancer research and clinical oncology · 2026

Longer-term response to SARS-CoV-2 vaccination after allogeneic blood stem cell transplantation.

Crodel Carl C, Gork Laura, Göpel Wibke, Linke Paul, Sinn Konrad, Miethke Jenny, Hochhaus Andreas, Hilgendorf Inken

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Аннотация

INTRODUCTION

Recipients of allogeneic haematopoietic stem cell transplantation (alloHSCT) are at increased risk of COVID-19 and lower vaccine immunogenicity. This study assessed vaccine immunogenicity and safety in these patients.

METHODS

We analyzed the serological response after the 2nd and 3rd SARS-CoV-2 vaccination as well as potential factors influencing this response. Data were obtained from internal hospital records. In addition, a questionnaire was used to evaluate the vaccination status, vaccination side effects and the course of expired COVID-19 disease.

RESULTS

In total, 114 patients (median age 62, range 27 - 70) were enrolled between July and September 2022, with 55 females (48.2%). One year later a follow up was conducted. Most patients (89.4%) were vaccinated at least twice, 66.7% received three vaccinations, and 10.5% refused the vaccination. The mRNA vaccines were predominantly used. Most patients responded and reached SARS-CoV-2 spike IgG titers after the 2nd (81.8%) or 3rd (96.1%) vaccination. Patients vaccinated within 24 months of alloHSCT had significantly lower anti-spike IgG levels than those vaccinated later (p=0.017). Common side effects included arm pain (34%), swelling (14%), and limb pain (17%).

CONCLUSION

Vaccination was feasible and well-tolerated in alloHSCT recipients. Timing of vaccination influenced immune response, with a stronger response after the 3rd dose compared to the initial series.

Для цитирования: Crodel Carl C, Gork Laura, Göpel Wibke, Linke Paul, Sinn Konrad, Miethke Jenny, Hochhaus Andreas, Hilgendorf Inken. Longer-term response to SARS-CoV-2 vaccination after allogeneic blood stem cell transplantation.. Journal of cancer research and clinical oncology. 2026. DOI: 10.1007/s00432-026-06632-4.

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