A non-genotoxic stem cell therapy boosts lymphopoiesis and averts age-related blood diseases in mice

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.

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Publication Details

Journal
Nature Communications
Published
2025-06-02
DOI
https://doi.org/10.1038/s41467-025-60464-3
Citations
3
Primary Topic
Hematopoietic Stem Cell Transplantation
Type
article
Field-Weighted Citation Impact
5.31

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article

A non-genotoxic stem cell therapy boosts lymphopoiesis and averts age-related blood diseases in mice

Anna Konturek-Cieśla, David Bryder, Qinyu Zhang, Shabnam Kharazi
3 citations
Nature Communications
Hematopoietic Stem Cell Transplantation
5.31
article

A non-genotoxic stem cell therapy boosts lymphopoiesis and averts age-related blood diseases in mice

Anna Konturek-Cieśla, David Bryder, Qinyu Zhang, Shabnam Kharazi
article en
3 citations

Abstract

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.

Nature CommunicationsVol. 16(1)
Lund University (SE), ETH Zurich (CH)
Cancerfonden, Lunds Universitet, Vetenskapsrådet, Kungliga Fysiografiska Sällskapet i Lund, Barncancerfonden
Openalex Percentile: Top 5%
Hematopoietic Stem Cell Transplantation
5.31
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A non-genotoxic stem cell therapy boosts lymphopoiesis and averts age-related blood diseases in mice — Anna Konturek-Cieśla, David Bryder, et al. · Nature Communications (2025) | TGRS Research Map | TGRS