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Lentiviral Gene Therapy Combined with Low-Dose Busulfan in Infants with SCID-X1.
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- Author(s): Mamcarz, E.; Triplett, B.; Janssen, W.; Gottschalk, S.; Dokmeci, E.; Love, J. T.; da Matta Ain, A. C.; van der Watt, H.; De Ravin, S. S.; Malech, H. L.; Long-Boyle, J. R.; Puck, J. M.; Cowan, M. J.; Mamcarz, Ewelina; Zhou, Sheng; Lockey, Timothy; Abdelsamed, Hossam; Cross, Shane J; Kang, Guolian; Ma, Zhijun
- Source:
New England Journal of Medicine. 4/18/2019, Vol. 380 Issue 16, p1525-1534. 10p. - Source:
- Additional Information
- Subject Terms: B cells; ANTIGENS; CELL receptors; CLINICAL trials; COMPARATIVE studies; GENE therapy; GENES; HEMATOPOIETIC stem cell transplantation; IMMUNOGLOBULINS; IMMUNOSUPPRESSION; KILLER cells; RESEARCH methodology; MEDICAL cooperation; RESEARCH; RESEARCH funding; RETROVIRUSES; T cells; EVALUATION research; SEVERE combined immunodeficiency; LYMPHOCYTE count; BUSULFAN; PHYSIOLOGY
- Abstract:
Background: Allogeneic hematopoietic stem-cell transplantation for X-linked severe combined immunodeficiency (SCID-X1) often fails to reconstitute immunity associated with T cells, B cells, and natural killer (NK) cells when matched sibling donors are unavailable unless high-dose chemotherapy is given. In previous studies, autologous gene therapy with γ-retroviral vectors failed to reconstitute B-cell and NK-cell immunity and was complicated by vector-related leukemia.Methods: We performed a dual-center, phase 1-2 safety and efficacy study of a lentiviral vector to transfer IL2RG complementary DNA to bone marrow stem cells after low-exposure, targeted busulfan conditioning in eight infants with newly diagnosed SCID-X1.Results: Eight infants with SCID-X1 were followed for a median of 16.4 months. Bone marrow harvest, busulfan conditioning, and cell infusion had no unexpected side effects. In seven infants, the numbers of CD3+, CD4+, and naive CD4+ T cells and NK cells normalized by 3 to 4 months after infusion and were accompanied by vector marking in T cells, B cells, NK cells, myeloid cells, and bone marrow progenitors. The eighth infant had an insufficient T-cell count initially, but T cells developed in this infant after a boost of gene-corrected cells without busulfan conditioning. Previous infections cleared in all infants, and all continued to grow normally. IgM levels normalized in seven of the eight infants, of whom four discontinued intravenous immune globulin supplementation; three of these four infants had a response to vaccines. Vector insertion-site analysis was performed in seven infants and showed polyclonal patterns without clonal dominance in all seven.Conclusions: Lentiviral vector gene therapy combined with low-exposure, targeted busulfan conditioning in infants with newly diagnosed SCID-X1 had low-grade acute toxic effects and resulted in multilineage engraftment of transduced cells, reconstitution of functional T cells and B cells, and normalization of NK-cell counts during a median follow-up of 16 months. (Funded by the American Lebanese Syrian Associated Charities and others; LVXSCID-ND ClinicalTrials.gov number, NCT01512888.). [ABSTRACT FROM AUTHOR] - Abstract: Copyright of New England Journal of Medicine is the property of New England Journal of Medicine and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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