The landscape of DDX41 mutations in blood diseases and the impact of donor-derived DDX41 variants on transplantation outcome

● Missense mutations P258L/Y259C are identified as the predominant Chinese-specific germline DDX41 variants. ● Pre-transplant DDX41 screening (VUS vs. P/LP) is recommended in related donors for better clinical outcomes. Germline variants of DDX41 were broadly investigated in myeloid neoplasms (MNs), while there is a lack of a larger cohort of Chinese patients report, and impact of donor-derived DDX41 variants on transplant outcomes has not been fully explored. We retrospectively analyzed 460 patients carrying DDX41 variants among 41 290 individuals. Although most of patients (65%) were diagnosed with MNs (mostly MDS/AML), other rarer diseases, such as AA, ALL, and lymphoma, can occur. A total of 417 germline and 262 somatic DDX41 variants were identified. The predominant pathogenic/likely pathogenic (P/LP) germline variants were P258L (26%) and Y259C (20%), followed by loss-of-function variants (25%) and c.935+4A>T (5%), which can cause aberrant intron retention. The most common somatic variants were R525H (53%), then G530D (7%) and T227M (4%). Germline variants in MNs were more often P/LP than in AA or ALL. GO (germline only) and GS (germline+somatic) mutations were distinctly distributed among diseases. Among thirteen donors included in this cohort, nine underwent transplantation. Four out of five recipients with donor-derived DDX41 -VUS variants continued to be in complete remission at 18 or 19 months after transplantation, compared to two out of four patients with donor-derived DDX41 -P/LP variants. For the first time, this study identified P258L/Y259C as predominant Chinese-specific germline DDX41 variants, expanding disease spectrum to include non-myeloid disorders, and established GS genotype as a key biomarker for myeloid malignancies. In addition, our results suggested that pre-transplant DDX41 germline screening in related donors may be beneficial for mitigating donor-derived leukemia and achieving better clinical outcomes.

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Publication Details

Journal
Blood Global Hematology
Published
2026-02-16
DOI
https://doi.org/10.1016/j.bglo.2026.100071
Primary Topic
Acute Myeloid Leukemia Research
Type
article
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article

The landscape of DDX41 mutations in blood diseases and the impact of donor-derived DDX41 variants on transplantation outcome

Yujiao Jia, Jigang Xiao, Jianxiang Wang, Chengwen Li et al.
Blood Global Hematology
Acute Myeloid Leukemia Research
article

The landscape of DDX41 mutations in blood diseases and the impact of donor-derived DDX41 variants on transplantation outcome

Yujiao Jia, Jigang Xiao, Jianxiang Wang, Chengwen Li, Hui Wei, Jianfeng Zhou, Ruixue Zhang, Shiqiang Qu, Li Qin, Zhijian Xiao, Qi Sun, Haoxu Wang, Erlie Jiang, Xiaoxue Han
article en

Abstract

● Missense mutations P258L/Y259C are identified as the predominant Chinese-specific germline DDX41 variants. ● Pre-transplant DDX41 screening (VUS vs. P/LP) is recommended in related donors for better clinical outcomes. Germline variants of DDX41 were broadly investigated in myeloid neoplasms (MNs), while there is a lack of a larger cohort of Chinese patients report, and impact of donor-derived DDX41 variants on transplant outcomes has not been fully explored. We retrospectively analyzed 460 patients carrying DDX41 variants among 41 290 individuals. Although most of patients (65%) were diagnosed with MNs (mostly MDS/AML), other rarer diseases, such as AA, ALL, and lymphoma, can occur. A total of 417 germline and 262 somatic DDX41 variants were identified. The predominant pathogenic/likely pathogenic (P/LP) germline variants were P258L (26%) and Y259C (20%), followed by loss-of-function variants (25%) and c.935+4A>T (5%), which can cause aberrant intron retention. The most common somatic variants were R525H (53%), then G530D (7%) and T227M (4%). Germline variants in MNs were more often P/LP than in AA or ALL. GO (germline only) and GS (germline+somatic) mutations were distinctly distributed among diseases. Among thirteen donors included in this cohort, nine underwent transplantation. Four out of five recipients with donor-derived DDX41 -VUS variants continued to be in complete remission at 18 or 19 months after transplantation, compared to two out of four patients with donor-derived DDX41 -P/LP variants. For the first time, this study identified P258L/Y259C as predominant Chinese-specific germline DDX41 variants, expanding disease spectrum to include non-myeloid disorders, and established GS genotype as a key biomarker for myeloid malignancies. In addition, our results suggested that pre-transplant DDX41 germline screening in related donors may be beneficial for mitigating donor-derived leukemia and achieving better clinical outcomes.

Blood Global HematologyVol. 2(2)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Kingmed Diagnostics (CN), Institute of Hematology & Blood Diseases Hospital (CN), Tianjin Medical University (CN)
Good health and well-being
Openalex Percentile: Top 53%
Acute Myeloid Leukemia Research
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