Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients

Steven J. Howe(Institute of Child Health), Marc R. Mansour(UCL Australia), Kerstin Schwarzwaelder(German Cancer Research Center), Cynthia C. Bartholomae(German Cancer Research Center), Michael Hubank(UCL Australia), Helena Kempski(Great Ormond Street Hospital), Martijn H. Brugman(Medizinische Hochschule Hannover), Karin Pike‐Overzet(Erasmus MC), S Chatters(Great Ormond Street Hospital), Dick de Ridder(Erasmus MC), Kimberly Gilmour(Great Ormond Street Hospital), Stuart Adams(Great Ormond Street Hospital), Susannah I. Thornhill(UCL Australia), Kathryn L. Parsley(Great Ormond Street Hospital), Frank J. T. Staal(Erasmus MC), Rosemary E. Gale(UCL Australia), David C. Linch(UCL Australia), Jinhua Bayford(Great Ormond Street Hospital), Lucie Brown(Great Ormond Street Hospital), Michelle Quaye(UCL Australia), Christine Kinnon(UCL Australia), Philip Ancliff(Great Ormond Street Hospital), David Webb(Great Ormond Street Hospital), Manfred Schmidt(German Cancer Research Center), Christof von Kalle(Translational Research in Oncology), H. Bobby Gaspar(Great Ormond Street Hospital), Adrian J. Thrasher(Great Ormond Street Hospital)
Journal of Clinical Investigation
August 6, 2008
Cited by 1,280Open Access
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Abstract

X-linked SCID (SCID-X1) is amenable to correction by gene therapy using conventional gammaretroviral vectors. Here, we describe the occurrence of clonal T cell acute lymphoblastic leukemia (T-ALL) promoted by insertional mutagenesis in a completed gene therapy trial of 10 SCID-X1 patients. Integration of the vector in an antisense orientation 35 kb upstream of the protooncogene LIM domain only 2 (LMO2) caused overexpression of LMO2 in the leukemic clone. However, leukemogenesis was likely precipitated by the acquisition of other genetic abnormalities unrelated to vector insertion, including a gain-of-function mutation in NOTCH1, deletion of the tumor suppressor gene locus cyclin-dependent kinase 2A (CDKN2A), and translocation of the TCR-beta region to the STIL-TAL1 locus. These findings highlight a general toxicity of endogenous gammaretroviral enhancer elements and also identify a combinatorial process during leukemic evolution that will be important for risk stratification and for future protocol design.


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