TY - JOUR
T1 - Hematopoietic reconstitution dynamics of mobilized- and bone marrow-derived human hematopoietic stem cells after gene therapy
AU - Scala, Serena
AU - Ferrua, Francesca
AU - Basso-Ricci, Luca
AU - Dionisio, Francesca
AU - Omrani, Maryam
AU - Quaranta, Pamela
AU - Jofra Hernandez, Raisa
AU - Del Core, Luca
AU - Benedicenti, Fabrizio
AU - Monti, Ilaria
AU - Giannelli, Stefania
AU - Fraschetta, Federico
AU - Darin, Silvia
AU - Albertazzi, Elena
AU - Galimberti, Stefania
AU - Montini, Eugenio
AU - Calabria, Andrea
AU - Cicalese, Maria Pia
AU - Aiuti, Alessandro
N1 - Funding Information:
This work was supported by Fondazione Telethon (TIGET Core Grant B2, A.A.), the Italian Ministero della Salute (Programma di Rete, NET-2011-02350069, A.A.), the European Commission (ERARE-3-JTC 2015 EUROCID, A.A.) and Else Kröner-Fresenius-Stiftung (EKFS) prize (A.A.). We thank F. Ciceri, ME Bernardo and all medical and nursing staff of the Pediatric Immunohematology and Bone Marrow Transplantation Unit of the San Raffaele Scientific Institute and the San Raffaele Stem Cell Programme; S. Zancan, M. Casiraghi, G. Tomaselli and all Sr-TIGET Clinical Trial Office personnel for clinical trial management and support; the OTL team for revising the manuscript; M. Gabaldo and G. Farinelli for support with project management; and P. Massariello, G. Vallanti, M. Manfredini and other MolMed staff for patient cell manipulation. We thank C. Waskow for her advice in handling NSGW41 mice. We thank C. Villa, E. Canonico and S. Di Terlizzi of the Flow Cytometry Resource, Advanced Cytometry Technical Applications Laboratory (FRACTAL) at Ospedale San Raffaele for cell sorting and technical help with instrumentation. We are indebted to the patients and their families for their commitment.
Funding Information:
This work was supported by Fondazione Telethon (TIGET Core Grant B2, A.A.), the Italian Ministero della Salute (Programma di Rete, NET-2011-02350069, A.A.), the European Commission (ERARE-3-JTC 2015 EUROCID, A.A.) and Else Kröner-Fresenius-Stiftung (EKFS) prize (A.A.). We thank F. Ciceri, ME Bernardo and all medical and nursing staff of the Pediatric Immunohematology and Bone Marrow Transplantation Unit of the San Raffaele Scientific Institute and the San Raffaele Stem Cell Programme; S. Zancan, M. Casiraghi, G. Tomaselli and all Sr-TIGET Clinical Trial Office personnel for clinical trial management and support; the OTL team for revising the manuscript; M. Gabaldo and G. Farinelli for support with project management; and P. Massariello, G. Vallanti, M. Manfredini and other MolMed staff for patient cell manipulation. We thank C. Waskow for her advice in handling NSGW41 mice. We thank C. Villa, E. Canonico and S. Di Terlizzi of the Flow Cytometry Resource, Advanced Cytometry Technical Applications Laboratory (FRACTAL) at Ospedale San Raffaele for cell sorting and technical help with instrumentation. We are indebted to the patients and their families for their commitment.
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/5/27
Y1 - 2023/5/27
N2 - Mobilized peripheral blood is increasingly used instead of bone marrow as a source of autologous hematopoietic stem/progenitor cells for ex vivo gene therapy. Here, we present an unplanned exploratory analysis evaluating the hematopoietic reconstitution kinetics, engraftment and clonality in 13 pediatric Wiskott-Aldrich syndrome patients treated with autologous lentiviral-vector transduced hematopoietic stem/progenitor cells derived from mobilized peripheral blood (n = 7), bone marrow (n = 5) or the combination of the two sources (n = 1). 8 out of 13 gene therapy patients were enrolled in an open-label, non-randomized, phase 1/2 clinical study (NCT01515462) and the remaining 5 patients were treated under expanded access programs. Although mobilized peripheral blood- and bone marrow- hematopoietic stem/progenitor cells display similar capability of being gene-corrected, maintaining the engineered grafts up to 3 years after gene therapy, mobilized peripheral blood-gene therapy group shows faster neutrophil and platelet recovery, higher number of engrafted clones and increased gene correction in the myeloid lineage which correlate with higher amount of primitive and myeloid progenitors contained in hematopoietic stem/progenitor cells derived from mobilized peripheral blood. In vitro differentiation and transplantation studies in mice confirm that primitive hematopoietic stem/progenitor cells from both sources have comparable engraftment and multilineage differentiation potential. Altogether, our analyses reveal that the differential behavior after gene therapy of hematopoietic stem/progenitor cells derived from either bone marrow or mobilized peripheral blood is mainly due to the distinct cell composition rather than functional differences of the infused cell products, providing new frames of references for clinical interpretation of hematopoietic stem/progenitor cell transplantation outcome.
AB - Mobilized peripheral blood is increasingly used instead of bone marrow as a source of autologous hematopoietic stem/progenitor cells for ex vivo gene therapy. Here, we present an unplanned exploratory analysis evaluating the hematopoietic reconstitution kinetics, engraftment and clonality in 13 pediatric Wiskott-Aldrich syndrome patients treated with autologous lentiviral-vector transduced hematopoietic stem/progenitor cells derived from mobilized peripheral blood (n = 7), bone marrow (n = 5) or the combination of the two sources (n = 1). 8 out of 13 gene therapy patients were enrolled in an open-label, non-randomized, phase 1/2 clinical study (NCT01515462) and the remaining 5 patients were treated under expanded access programs. Although mobilized peripheral blood- and bone marrow- hematopoietic stem/progenitor cells display similar capability of being gene-corrected, maintaining the engineered grafts up to 3 years after gene therapy, mobilized peripheral blood-gene therapy group shows faster neutrophil and platelet recovery, higher number of engrafted clones and increased gene correction in the myeloid lineage which correlate with higher amount of primitive and myeloid progenitors contained in hematopoietic stem/progenitor cells derived from mobilized peripheral blood. In vitro differentiation and transplantation studies in mice confirm that primitive hematopoietic stem/progenitor cells from both sources have comparable engraftment and multilineage differentiation potential. Altogether, our analyses reveal that the differential behavior after gene therapy of hematopoietic stem/progenitor cells derived from either bone marrow or mobilized peripheral blood is mainly due to the distinct cell composition rather than functional differences of the infused cell products, providing new frames of references for clinical interpretation of hematopoietic stem/progenitor cell transplantation outcome.
UR - http://www.scopus.com/inward/record.url?scp=85160243442&partnerID=8YFLogxK
U2 - 10.1038/s41467-023-38448-y
DO - 10.1038/s41467-023-38448-y
M3 - Article
C2 - 37244942
AN - SCOPUS:85160243442
SN - 2041-1723
VL - 14
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 3068
ER -