Author
Listed:
- Agnieszka Czechowicz
(Boston Children’s Hospital
Dana Farber Cancer Institute
Harvard Medical School
Harvard University)
- Rahul Palchaudhuri
(Harvard University
Harvard Stem Cell Institute
Massachusetts General Hospital
Harvard University)
- Amelia Scheck
(Boston Children’s Hospital
Harvard Medical School
Harvard University
Harvard Stem Cell Institute)
- Yu Hu
(Boston Children’s Hospital)
- Jonathan Hoggatt
(Harvard University
Harvard Stem Cell Institute
Massachusetts General Hospital)
- Borja Saez
(Harvard University
Harvard Stem Cell Institute
Massachusetts General Hospital
Center For Applied Medical Research)
- Wendy W. Pang
(Stanford University School of Medicine
Stanford University School of Medicine
Stanford University School of Medicine
Stanford University School of Medicine)
- Michael K. Mansour
(Harvard University
Harvard Stem Cell Institute
Massachusetts General Hospital
Massachusetts General Hospital)
- Tiffany A. Tate
(Harvard University
Harvard Stem Cell Institute
Massachusetts General Hospital)
- Yan Yi Chan
(Stanford University School of Medicine
Stanford University School of Medicine)
- Emily Walck
(Stanford University School of Medicine
Stanford University School of Medicine)
- Gerlinde Wernig
(Stanford University School of Medicine
Stanford University School of Medicine)
- Judith A. Shizuru
(Stanford University School of Medicine
Stanford University School of Medicine
Stanford University School of Medicine)
- Florian Winau
(Boston Children’s Hospital)
- David T. Scadden
(Harvard University
Harvard Stem Cell Institute
Massachusetts General Hospital)
- Derrick J. Rossi
(Boston Children’s Hospital
Harvard Medical School
Harvard University
Harvard Stem Cell Institute)
Abstract
Hematopoietic stem cell transplantation (HSCT) is a curative therapy for blood and immune diseases with potential for many settings beyond current standard-of-care. Broad HSCT application is currently precluded largely due to morbidity and mortality associated with genotoxic irradiation or chemotherapy conditioning. Here we show that a single dose of a CD117-antibody-drug-conjugate (CD117-ADC) to saporin leads to > 99% depletion of host HSCs, enabling rapid and efficient donor hematopoietic cell engraftment. Importantly, CD117-ADC selectively targets hematopoietic stem cells yet does not cause clinically significant side-effects. Blood counts and immune cell function are preserved following CD117-ADC treatment, with effective responses by recipients to both viral and fungal challenges. These results suggest that CD117-ADC-mediated HSCT pre-treatment could serve as a non-myeloablative conditioning strategy for the treatment of a wide range of non-malignant and malignant diseases, and might be especially suited to gene therapy and gene editing settings in which preservation of immunity is desired.
Suggested Citation
Agnieszka Czechowicz & Rahul Palchaudhuri & Amelia Scheck & Yu Hu & Jonathan Hoggatt & Borja Saez & Wendy W. Pang & Michael K. Mansour & Tiffany A. Tate & Yan Yi Chan & Emily Walck & Gerlinde Wernig &, 2019.
"Selective hematopoietic stem cell ablation using CD117-antibody-drug-conjugates enables safe and effective transplantation with immunity preservation,"
Nature Communications, Nature, vol. 10(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-018-08201-x
DOI: 10.1038/s41467-018-08201-x
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