A1 Refereed original research article in a scientific journal
Donor genetic determinant of thymopoiesis, rs2204985, and stem cell transplantation outcome in a multipopulation cohort
Authors: Nihtilä Julia, Salmenniemi Urpu, Itälä-Remes Maija, Crossland Rachel E, Gallardo David, Bogunia-Kubik Katarzyna, Łacina Piotr, Bieniaszewska Maria, Giebel Sebastian, Hyvärinen Kati, Kekäläinen Eliisa, Ritari Jarmo, Partanen Jukka
Publisher: Elsevier
Publication year: 2024
Journal: Human Immunology
Journal name in source: Human Immunology
Article number: 110791
Volume: 85
Issue: 3
ISSN: 0198-8859
eISSN: 1879-1166
DOI: https://doi.org/10.1016/j.humimm.2024.110791
Web address : https://doi.org/10.1016/j.humimm.2024.110791
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/387508015
Background: A genetic polymorphism, rs2204985, has been reported to be associated with the diversity of T-cell antigen receptor repertoire and TREC levels, reflecting the function of the thymus. As the thymus function can be assumed to be an important factor regulating the outcome of stem cell transplantation (SCT), it was of great interest that rs2204985 showed a genetic association to disease-free and overall survival in a German SCT donor cohort. Tools to predict the outcome of SCT more accurately would help in risk assessment and patient safety.
Objective: To evaluate the general validity of the original genetic association found in the German cohort, we determined genetic associations between rs2204985 and the outcome of SCT in 1,473 SCT donors from four different populations.
Study design: Genetic associations between rs2204985 genotype AA versus AG/GG and overall survival (OS) and disease-free survival (DFS) in 1,473 adult, allogeneic SCT from Finland, the United Kingdom, Spain, and Poland were performed using the Kaplan-Meier analysis and log-rank tests. We adjusted the survival models with covariates using Cox regression.
Results: In unrelated SCT donors (N = 425), the OS of genotype AA versus AG/GG had a trend for a similar association (p = 0.049, log-rank test) as previously reported in the German cohort. The trend did not remain significant in the Cox regression analysis with covariates. No other associations were found.
Conclusion: Weak support for the genetic association between rs2204985, previously also associated with thymus function, and the outcome of SCT could be found in a cohort from four populations.
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Funding information in the publication:
The present study was supported by research grants from the TEKES (currently Business Finland) for the SalWe project (for JP), the Academy of Finland (for JP), Cancer Foundation Finland (for JP and JR), VTR funding from the Government of Finland to the Blood Service, COST Eurograft ActionCA17138 (for K B-K, PL, JN, JP, RC), the National Science Centre (Poland) (grant No. 2018/31/B/NZ2/03065) (for K B-K, PL, MB and SG), National Institute of Health Carlos III (ISCIII) (Spain), co-funded by the European Union (grants number PI17/00815 and PI20/01353) (for DG), and Newcastle Hospitals Charity (REC).