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Gene Therapy for Nonmalignant Hematology

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Cell and Gene Therapies

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Abstract

Hematopoietic stem cell (HSC) gene therapy has effectively become a therapeutic option largely due to the resounding clinical successes in patients with primary immunodeficiencies (PIDs) such as X-linked severe immunodeficiency (SCID-X1), adenosine deaminase deficiency (ADA-SCID), Wiskott-Aldrich syndrome (WAS), and chronic granulomatous disease (CGD). HSC gene therapy is also being investigated in patients with metabolic diseases such as X-linked adrenoleukodystrophy (ALD) and metachromatic leukodystrophy (MLD) and inherited blood disorders such as β-thalassemia and sickle cell disease (SCD) where some therapeutic benefits have been reported more recently. Safer and more efficient self-inactivating (SIN) γ-retroviral and lentiviral vectors have been developed to overcome the genotoxicity imparted by γ-retroviral vectors with intact long terminal repeat (LTR). The discovery and maturation of gene-editing platforms, including zinc-finger nuclease (ZFN), transcription activator-like effector nucleases (TALEN), and clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9, offer exciting prospective strategies for further improving gene therapy by targeting the repair of diseased genes.

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Acknowledgments

We thank Michel Sadelain, MD, PhD, for reviewing the manuscript.

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Authors and Affiliations

  1. Michael G. Harris Cell Therapy and Cell Engineering Facility, Center for Cell Engineering, New York, NY, USA

    Xiuyan Wang & Isabelle Rivière

  2. Molecular Pharmacology Program, Memorial Sloan-Kettering Cancer Center, New York, NY, USA

    Xiuyan Wang & Isabelle Rivière

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  1. Xiuyan Wang
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  2. Isabelle Rivière
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Correspondence to Isabelle Rivière .

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Editors and Affiliations

  1. Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA

    Miguel-Angel Perales

  2. Cancer Treatment Centers of America, Deerfield, IL, USA

    Syed A. Abutalib

  3. Center for Cancer and Immunology Research Children’s National and The George Washington University, Division Allergy and Immunology, Washington, DC, USA

    Catherine Bollard

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Wang, X., Rivière, I. (2019). Gene Therapy for Nonmalignant Hematology. In: Perales, MA., Abutalib, S., Bollard, C. (eds) Cell and Gene Therapies. Advances and Controversies in Hematopoietic Transplantation and Cell Therapy. Springer, Cham. https://doi.org/10.1007/978-3-319-54368-0_14

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