Literature DB >> 27431943

Preclinical Testing of the Safety and Tolerability of Lentiviral Vector-Mediated Above-Normal Alpha-L-Iduronidase Expression in Murine and Human Hematopoietic Cells Using Toxicology and Biodistribution Good Laboratory Practice Studies.

Ilaria Visigalli1, Stefania Delai1, Francesca Ferro1, Francesca Cecere1, Michela Vezzoli1, Francesca Sanvito1,2, Franck Chanut3,4, Fabrizio Benedicenti1, Giulio Spinozzi1, Rob Wynn5, Andrea Calabria1, Luigi Naldini1,6, Eugenio Montini1, Patrizia Cristofori1,3, Alessandra Biffi1.   

Abstract

In order to support the clinical application of hematopoietic stem cell (HSC) gene therapy for mucopolysaccharidosis I (MPS I), biosafety studies were conducted to assess the toxicity and tumorigenic potential, as well as the biodistribution of HSCs and progenitor cells (HSPCs) transduced with lentiviral vectors (LV) encoding the cDNA of the alpha-iduronidase (IDUA) gene, which is mutated in MPS I patients. To this goal, toxicology and biodistribution studies were conducted, employing Good Laboratory Practice principles. Vector integration site (IS) studies were applied in order to predict adverse consequences of vector gene transfer and to obtain HSC-related information. Overall, the results obtained in these studies provided robust evidence to support the safety and tolerability of high-efficiency LV-mediated gene transfer and above-normal IDUA enzyme expression in both murine and human HSPCs and their in vivo progeny. Taken together, these investigations provide essential safety data to support clinical testing of HSC gene therapy in MPS I patients. These studies also underline criticisms associated with the use of currently available models, and highlight the value of surrogate markers of tumorigenicity that may be further explored in the future. Notably, biological evidence supporting the efficacy of gene therapy on MPS I disease and its feasibility on patients' HSCs were also generated, employing clinical-grade LVs. Finally, the clonal contribution of LV-transduced HSPCs to hematopoiesis along serial transplantation was quantified in a minimum of 200-300 clones, with the different level of repopulating cells in primary recipients being reflected in the secondary.

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Year:  2016        PMID: 27431943     DOI: 10.1089/hum.2016.068

Source DB:  PubMed          Journal:  Hum Gene Ther        ISSN: 1043-0342            Impact factor:   5.695


  19 in total

Review 1.  Hematopoietic Stem Cell Gene Therapy for Storage Disease: Current and New Indications.

Authors:  Alessandra Biffi
Journal:  Mol Ther       Date:  2017-04-04       Impact factor: 11.454

2.  Hepatotoxicity and Toxicology of In Vivo Lentiviral Vector Administration in Healthy and Liver-Injury Mouse Models.

Authors:  Robert Allen Kaiser; Clara Teresa Nicolas; Kari Lynn Allen; Jennifer Anne Chilton; Zeji Du; Raymond Daniel Hickey; Joseph Benjamin Lillegard
Journal:  Hum Gene Ther Clin Dev       Date:  2019-04-11       Impact factor: 5.032

Review 3.  A Historical Review of Brain Drug Delivery.

Authors:  William M Pardridge
Journal:  Pharmaceutics       Date:  2022-06-16       Impact factor: 6.525

Review 4.  Brain Delivery of Nanomedicines: Trojan Horse Liposomes for Plasmid DNA Gene Therapy of the Brain.

Authors:  William M Pardridge
Journal:  Front Med Technol       Date:  2020-11-16

5.  VISPA2: a scalable pipeline for high-throughput identification and annotation of vector integration sites.

Authors:  Giulio Spinozzi; Andrea Calabria; Stefano Brasca; Stefano Beretta; Ivan Merelli; Luciano Milanesi; Eugenio Montini
Journal:  BMC Bioinformatics       Date:  2017-11-25       Impact factor: 3.169

Review 6.  Open issues in Mucopolysaccharidosis type I-Hurler.

Authors:  Rossella Parini; Federica Deodato; Maja Di Rocco; Edoardo Lanino; Franco Locatelli; Chiara Messina; Attilio Rovelli; Maurizio Scarpa
Journal:  Orphanet J Rare Dis       Date:  2017-06-15       Impact factor: 4.123

Review 7.  Mitochondrial Neurogastrointestinal Encephalomyopathy Caused by Thymidine Phosphorylase Enzyme Deficiency: From Pathogenesis to Emerging Therapeutic Options.

Authors:  Rana Yadak; Peter Sillevis Smitt; Marike W van Gisbergen; Niek P van Til; Irenaeus F M de Coo
Journal:  Front Cell Neurosci       Date:  2017-02-15       Impact factor: 5.505

Review 8.  Gene therapy for mucopolysaccharidoses: in vivo and ex vivo approaches.

Authors:  Alessandro Fraldi; Marta Serafini; Nicolina Cristina Sorrentino; Bernhard Gentner; Alessandro Aiuti; Maria Ester Bernardo
Journal:  Ital J Pediatr       Date:  2018-11-16       Impact factor: 2.638

Review 9.  Gene therapy for lysosomal storage disorders: recent advances for metachromatic leukodystrophy and mucopolysaccaridosis I.

Authors:  Rachele Penati; Francesca Fumagalli; Valeria Calbi; Maria Ester Bernardo; Alessandro Aiuti
Journal:  J Inherit Metab Dis       Date:  2017-05-30       Impact factor: 4.982

10.  Lentiviral Hematopoietic Stem Cell Gene Therapy Rescues Clinical Phenotypes in a Murine Model of Pompe Disease.

Authors:  Giuseppa Piras; Claudia Montiel-Equihua; Yee-Ka Agnes Chan; Slawomir Wantuch; Daniel Stuckey; Derek Burke; Helen Prunty; Rahul Phadke; Darren Chambers; Armando Partida-Gaytan; Diego Leon-Rico; Neelam Panchal; Kathryn Whitmore; Miguel Calero; Sara Benedetti; Giorgia Santilli; Adrian J Thrasher; H Bobby Gaspar
Journal:  Mol Ther Methods Clin Dev       Date:  2020-07-06       Impact factor: 6.698

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