Skip to main navigation Skip to search Skip to main content

Lentiviral Gene Therapy for Artemis-Deficient SCID

  • Morton J. Cowan
  • , Jason Yu
  • , Janelle Facchino
  • , Carol Fraser-Browne
  • , Ukina Sanford
  • , Misako Kawahara
  • , Jasmeen Dara
  • , Janel Long-Boyle
  • , Jess Oh
  • , Wendy Chan
  • , Shivali Chag
  • , Lori Broderick
  • , Deepak Chellapandian
  • , Hélène Decaluwe
  • , Catherine Golski
  • , Diana Hu
  • , Caroline Y. Kuo
  • , Holly K. Miller
  • , Aleksandra Petrovic
  • , Robert Currier
  • Joan F. Hilton, Divya Punwani, Christopher C. Dvorak, Harry L. Malech, R. Scott Mcivor, Jennifer M. Puck

Research output: Contribution to journal › Article › peer-review

Abstract

Background The DNA-repair enzyme Artemis is essential for rearrangement of T- and B-cell receptors. Mutations in DCLRE1C, which encodes Artemis, cause Artemis-deficient severe combined immunodeficiency (ART-SCID), which is poorly responsive to allogeneic hematopoietic-cell transplantation. Methods We carried out a phase 1-2 clinical study of the transfusion of autologous CD34+ cells, transfected with a lentiviral vector containing DCLRE1C, in 10 infants with newly diagnosed ART-SCID. We followed them for a median of 31.2 months. Results Marrow harvest, busulfan conditioning, and lentiviral-transduced CD34+ cell infusion produced the expected grade 3 or 4 adverse events. All the procedures met prespecified criteria for feasibility at 42 days after infusion. Gene-marked T cells were detected at 6 to 16 weeks after infusion in all the patients. Five of 6 patients who were followed for at least 24 months had T-cell immune reconstitution at a median of 12 months. The diversity of T-cell receptor β chains normalized by 6 to 12 months. Four patients who were followed for at least 24 months had sufficient B-cell numbers, IgM concentration, or IgM isohemagglutinin titers to permit discontinuation of IgG infusions. Three of these 4 patients had normal immunization responses, and the fourth has started immunizations. Vector insertion sites showed no evidence of clonal expansion. One patient who presented with cytomegalovirus infection received a second infusion of gene-corrected cells to achieve T-cell immunity sufficient for viral clearance. Autoimmune hemolytic anemia developed in 4 patients 4 to 11 months after infusion; this condition resolved after reconstitution of T-cell immunity. All 10 patients were healthy at the time of this report. Conclusions Infusion of lentiviral gene-corrected autologous CD34+ cells, preceded by pharmacologically targeted low-exposure busulfan, in infants with newly diagnosed ART-SCID resulted in genetically corrected and functional T and B cells. (Funded by the California Institute for Regenerative Medicine and the National Institute of Allergy and Infectious Diseases; ClinicalTrials.gov number, NCT03538899.).

Original languageEnglish (US)
Pages (from-to)2344-2355
Number of pages12
JournalNew England Journal of Medicine
Volume387
Issue number25
DOIs
StatePublished - Dec 22 2022

Bibliographical note

Funding Information:
Supported by grants from the California Institute for Regenerative Medicine (CLIN2-10830, to Drs. Cowan and Puck) and the National Institute of Allergy and Infectious Diseases ( NIAID ) (U54-AI082973, to Drs. Cowan, Dvorak, and Puck) and intramural NIAID (to Dr. Malech). Drs. Cowan and Puck receive support from the UCSF Smith Cardiovascular Research Institute, and Dr. Puck receives support from the NIAID (P01-AI138962) and the Lisa and Douglas Goldman Fund.

Publisher Copyright:
© 2022 Massachusetts Medical Society.

Keywords

  • Allergy/Immunology
  • Allergy/Immunology General
  • Bone Marrow Transplantation
  • Childhood Diseases
  • Genetics
  • Genetics General
  • Hematology/Oncology
  • Hematology/Oncology General
  • Immunity
  • Immunodeficiency
  • Infectious Disease
  • Infectious Disease General
  • Pediatrics
  • Pediatrics General
  • T-Cells

Fingerprint

Dive into the research topics of 'Lentiviral Gene Therapy for Artemis-Deficient SCID'. Together they form a unique fingerprint.

Cite this