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Influence of FOXP3 single-nucleotide polymorphism after allogeneic hematopoietic stem cell transplantation

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Abstract

The impact of FOXP3 single-nucleotide polymorphisms (SNP) on clinical outcomes after allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains poorly understood. We investigated the relationship between a FOXP3 SNP (rs3761548) and clinical outcomes in 91 patients with hematological malignancies after allo-HSCT. Multivariate analysis showed that risk of severe chronic graft-versus-host disease (cGVHD) was significantly higher in patients with the FOXP3-3279C/A or FOXP3-3279A/A genotype than those with the FOXP3-3279C/C genotype [hazard ratio (HR), 2.69; 95% confidence interval (CI) 1.14–6.31; p = 0.023]. Therefore, FOXP3 at SNP rs3761548 can be a useful marker for predicting the occurrence of severe cGVHD.

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Data availability

The data that support the findings of the current study are available from the corresponding author, N.H, upon reasonable request.

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Acknowledgements

The authors thank all patients and clinical staff members who contributed to this study.

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Contributions

NH contributed to the study’s conception and design. Material preparation, data collection, and analysis were performed by MS, KK, and NH. The first draft of the manuscript was written by KK and NH, and all authors commented on previous versions of the manuscript. All authors have read and approved the final manuscript.

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Correspondence to Norimichi Hattori.

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Supplementary file1 (XLSX 15 KB): Table S1. Baseline characteristics of patients.

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Kuroiwa, K., Sato, M., Narita, H. et al. Influence of FOXP3 single-nucleotide polymorphism after allogeneic hematopoietic stem cell transplantation. Int J Hematol 119, 583–591 (2024). https://doi.org/10.1007/s12185-024-03726-y

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  • DOI: https://doi.org/10.1007/s12185-024-03726-y

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