Donor leukocyte telomere length emerges as a prognostic factor for transplantation outcomes
Younger donors are preferred in allogeneic hematopoietic stem cell transplantation (allo-HSCT), but this preference may limit access for patients whose only available donors are older. This study evaluated whether donor leukocyte telomere length (LTL), in conjunction with donor age, refines donor selection strategies to improve outcomes in recipients with acute leukemia. The discovery analysis included 1,049 acute leukemia patients who underwent allo-HSCT at the First Affiliated Hospital of Zhejiang University School of Medicine, while the replication cohort included 153 recipients from three additional centers. Donor LTL was measured using real-time quantitative PCR and categorized into quartiles: short (Q1) and long (Q2-Q4). Donor age was prespecified as <40 (younger) vs. ≥40 (older) years based on clinical practice. Long donor LTL was associated with a lower cumulative incidence of relapse (CIR), improved overall survival (OS), and better relapse-free survival (RFS) in allo-HSCT recipients. Recipients of grafts from donors aged ≥40 years with short LTL had higher CIR (adjusted hazard ratio [aHR] = 1.51; 95% confidence interval [CI], 1.04-2.19), worse OS (aHR = 1.76; 95% CI, 1.20-2.58), and worse RFS (aHR = 1.53; 95% CI, 1.06-2.20) compared with recipients of grafts from donors <40 years. Immune cell profiling showed that older donors with short LTL had more CD8<sup>+</sup>CD57<sup>+</sup>HLA-DR<sup>-</sup> cells. In the replication cohort, recipients of grafts from older donors with long LTL had outcomes comparable with those of recipients with younger donors, while those with older donors and short LTL had inferior outcomes. These findings support considering donor LTL as a supplemental factor during donor evaluation, especially when younger donors are not available.
Authors
- Ruowen Wei (ORCID: https://orcid.org/0000-0002-9852-5010)
- Pengxu Qian (ORCID: https://orcid.org/0000-0001-5636-6704)
- Xiaoyu Lai (ORCID: https://orcid.org/0000-0002-3093-8476)
- Xiaoxia Hu (ORCID: https://orcid.org/0000-0002-2719-3805)
- Jimin Shi (ORCID: https://orcid.org/0000-0002-1852-326X)
- Yunxian Yu (ORCID: https://orcid.org/0000-0002-3394-9832)
- Yamin Tan (ORCID: https://orcid.org/0009-0003-6120-8649)
- Zhuoyue Shi
- Yi Luo (ORCID: https://orcid.org/0000-0002-6877-9327)
- Zhongzheng Zheng
- Yanmin Zhao (ORCID: https://orcid.org/0000-0003-3857-5574)
- Hengwei Wu (ORCID: https://orcid.org/0000-0002-0476-8370)
- Yang Cao (ORCID: https://orcid.org/0000-0001-7787-8506)
- Wei Shi (ORCID: https://orcid.org/0000-0002-6146-5894)
- He Huang (ORCID: https://orcid.org/0000-0002-2723-1621)
- Huarui Fu
- Jing Yu (ORCID: https://orcid.org/0000-0002-6723-5352)
- Wenming Shi (ORCID: https://orcid.org/0000-0002-4054-8500)
- Jian Yu
- Lizhen Liu
Institutions
- Union Hospital (HK)
- Shanghai Jiao Tong University (CN)
- Ruijin Hospital (CN)
- Cell Technology (China) (HK)
- Precision for Medicine (United States) (US)
- Cancer Hospital of Chinese Academy of Medical Sciences (CN)
- HKU-Pasteur Research Pole (HK)
- Shanghai Institute of Hematology (CN)
- Tongji Hospital (CN)
- First Affiliated Hospital Zhejiang University (CN)
- Huazhong University of Science and Technology (CN)
- Zhejiang University (CN)
- University of Hong Kong (HK)
Publication Details
- Journal
- The Innovation
- Published
- 2025-10-25
- DOI
- https://doi.org/10.1016/j.xinn.2025.101147
- Primary Topic
- Telomeres, Telomerase, and Senescence
- Type
- article
- Field-Weighted Citation Impact
- 0.00