Literature DB >> 33974366

Autologous Ex Vivo Lentiviral Gene Therapy for Adenosine Deaminase Deficiency.

Donald B Kohn1, Claire Booth1, Kit L Shaw1, Jinhua Xu-Bayford1, Elizabeth Garabedian1, Valentina Trevisan1, Denise A Carbonaro-Sarracino1, Kajal Soni1, Dayna Terrazas1, Katie Snell1, Alan Ikeda1, Diego Leon-Rico1, Theodore B Moore1, Karen F Buckland1, Ami J Shah1, Kimberly C Gilmour1, Satiro De Oliveira1, Christine Rivat1, Gay M Crooks1, Natalia Izotova1, John Tse1, Stuart Adams1, Sally Shupien1, Hilory Ricketts1, Alejandra Davila1, Chilenwa Uzowuru1, Amalia Icreverzi1, Provaboti Barman1, Beatriz Campo Fernandez1, Roger P Hollis1, Maritess Coronel1, Allen Yu1, Krista M Chun1, Christian E Casas1, Ruixue Zhang1, Serena Arduini1, Frances Lynn1, Mahesh Kudari1, Andrea Spezzi1, Marco Zahn1, Rene Heimke1, Ivan Labik1, Roberta Parrott1, Rebecca H Buckley1, Lilith Reeves1, Kenneth Cornetta1, Robert Sokolic1, Michael Hershfield1, Manfred Schmidt1, Fabio Candotti1, Harry L Malech1, Adrian J Thrasher1, H Bobby Gaspar1.   

Abstract

BACKGROUND: Severe combined immunodeficiency due to adenosine deaminase (ADA) deficiency (ADA-SCID) is a rare and life-threatening primary immunodeficiency.
METHODS: We treated 50 patients with ADA-SCID (30 in the United States and 20 in the United Kingdom) with an investigational gene therapy composed of autologous CD34+ hematopoietic stem and progenitor cells (HSPCs) transduced ex vivo with a self-inactivating lentiviral vector encoding human ADA. Data from the two U.S. studies (in which fresh and cryopreserved formulations were used) at 24 months of follow-up were analyzed alongside data from the U.K. study (in which a fresh formulation was used) at 36 months of follow-up.
RESULTS: Overall survival was 100% in all studies up to 24 and 36 months. Event-free survival (in the absence of reinitiation of enzyme-replacement therapy or rescue allogeneic hematopoietic stem-cell transplantation) was 97% (U.S. studies) and 100% (U.K. study) at 12 months; 97% and 95%, respectively, at 24 months; and 95% (U.K. study) at 36 months. Engraftment of genetically modified HSPCs persisted in 29 of 30 patients in the U.S. studies and in 19 of 20 patients in the U.K. study. Patients had sustained metabolic detoxification and normalization of ADA activity levels. Immune reconstitution was robust, with 90% of the patients in the U.S. studies and 100% of those in the U.K. study discontinuing immunoglobulin-replacement therapy by 24 months and 36 months, respectively. No evidence of monoclonal expansion, leukoproliferative complications, or emergence of replication-competent lentivirus was noted, and no events of autoimmunity or graft-versus-host disease occurred. Most adverse events were of low grade.
CONCLUSIONS: Treatment of ADA-SCID with ex vivo lentiviral HSPC gene therapy resulted in high overall and event-free survival with sustained ADA expression, metabolic correction, and functional immune reconstitution. (Funded by the National Institutes of Health and others; ClinicalTrials.gov numbers, NCT01852071, NCT02999984, and NCT01380990.).
Copyright © 2021 Massachusetts Medical Society.

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Year:  2021        PMID: 33974366      PMCID: PMC8240285          DOI: 10.1056/NEJMoa2027675

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  31 in total

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