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Improved collection of hematopoietic stem cells and progenitors from Fanconi anemia patients for gene therapy purposes.

Authors :
Sevilla J
Navarro S
Rio P
Sánchez-Domínguez R
Zubicaray J
Gálvez E
Merino E
Sebastián E
Azqueta C
Casado JA
Segovia JC
Alberquilla O
Bogliolo M
Román-Rodríguez FJ
Giménez Y
Larcher L
Salgado R
Pujol RM
Hladun R
Castillo A
Soulier J
Querol S
Fernández J
Schwartz J
García de Andoín N
López R
Catalá A
Surralles J
Díaz-de-Heredia C
Bueren JA
Source :
Molecular therapy. Methods & clinical development [Mol Ther Methods Clin Dev] 2021 Jun 12; Vol. 22, pp. 66-75. Date of Electronic Publication: 2021 Jun 12 (Print Publication: 2021).
Publication Year :
2021

Abstract

Difficulties in the collection of hematopoietic stem and progenitor cells (HSPCs) from Fanconi anemia (FA) patients have limited the gene therapy in this disease. We have investigated (ClinicalTrials.gov, NCT02931071) the safety and efficacy of filgrastim and plerixafor for mobilization of HSPCs and collection by leukapheresis in FA patients. Nine of eleven enrolled patients mobilized beyond the threshold level of 5 CD34 <superscript>+</superscript> cells/μL required to initiate apheresis. A median of 21.8 CD34 <superscript>+</superscript> cells/μL was reached at the peak of mobilization. Significantly, the oldest patients (15 and 16 years old) were the only ones who did not reach that threshold. A median of 4.27 million CD34 <superscript>+</superscript> cells/kg was collected in 2 or 3 aphereses. These numbers were markedly decreased to 1.1 million CD34 <superscript>+</superscript> cells/kg after immunoselection, probably because of weak expression of the CD34 antigen. However, these numbers were sufficient to facilitate the engraftment of corrected HSPCs in non-conditioned patients. No procedure-associated serious adverse events were observed. Mobilization of CD34 <superscript>+</superscript> cells correlated with younger age, higher leukocyte counts and hemoglobin values, lower mean corpuscular volume, and higher proportion of CD34 <superscript>+</superscript> cells in bone marrow (BM). All these values offer crucial information for the enrollment of FA patients for gene therapy protocols.<br />Competing Interests: J. Sevilla is a consultant and advisor and has received honorarium (Amgen, Novartis, Miltenyi, Sobi, Rocket Pharmaceuticals Inc.) and has licensed medicinal products from Rocket Pharmaceuticals Inc. S.N. and P.R. have licensed medicinal products and receive research funding and equity from Rocket Pharmaceuticals Inc. J.C.S.: Rocket Pharmaceuticals Inc.: consultant/incomes from licensed medicinal products/research funding/equity. J. Schwartz is Medical Director of Rocket Pharmaceuticals Inc. J. Surralles: service agreements (Rocket Pharmaceuticals Inc.). J.A.B.: Rocket Pharmaceuticals Inc.: consultant/incomes from licensed medicinal products/research funding/equity; Roche: honorarium; Pfizer: honorarium.<br /> (© 2021 The Author(s).)

Details

Language :
English
ISSN :
2329-0501
Volume :
22
Database :
MEDLINE
Journal :
Molecular therapy. Methods & clinical development
Publication Type :
Academic Journal
Accession number :
34485595
Full Text :
https://doi.org/10.1016/j.omtm.2021.06.001