Konturek-Ciesla Anna, Zhang Qinyu, Kharazi Shabnam, Bryder David
Division of Molecular Hematology, Department of Laboratory Medicine, Lund Stem Cell Center, Medical Faculty, Lund University, Lund, Sweden.
Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
Nat Commun. 2025 Jun 2;16(1):5129. doi: 10.1038/s41467-025-60464-3.
Hematopoietic stem cell (HSC) transplantation offers a cure for a variety of blood disorders, predominantly affecting the elderly; however, its application, especially in this demographic, is limited by treatment toxicity. In response, we employ a murine transplantation model based on low-intensity conditioning protocols using antibody-mediated HSC depletion. While aging presents a significant barrier to effective HSC engraftment, optimizing HSC doses and non-genotoxic targeting methods greatly enhance the long-term multilineage activity of the transplanted cells. We demonstrate that young HSCs, once effectively engrafted in aged hosts, improve hematopoietic output and ameliorate age-compromised lymphopoiesis. This culminated in a strategy that robustly mitigates disease progression in a genetic model of myelodysplastic syndrome. These results suggest that non-genotoxic HSC transplantation could fundamentally change the clinical management of age-associated hematological disorders, offering a prophylactic tool to delay or even prevent their onset in elderly patients.
造血干细胞(HSC)移植为多种血液疾病提供了治愈方法,这些疾病主要影响老年人;然而,其应用,尤其是在这一人群中的应用,受到治疗毒性的限制。作为回应,我们采用了一种基于低强度预处理方案的小鼠移植模型,该方案使用抗体介导的HSC清除。虽然衰老对有效的HSC植入构成了重大障碍,但优化HSC剂量和非基因毒性靶向方法可大大增强移植细胞的长期多谱系活性。我们证明,年轻的HSCs一旦有效地植入老年宿主中,可改善造血输出并改善年龄相关的淋巴细胞生成受损情况。这最终形成了一种策略,可有力地减轻骨髓增生异常综合征遗传模型中的疾病进展。这些结果表明,非基因毒性HSC移植可能从根本上改变与年龄相关的血液疾病的临床管理,为延迟甚至预防老年患者发病提供一种预防性工具。