Development of gene therapy: potential in severe combined immunodeficiency due to adenosine deaminase deficiency
Author(s) -
Adrian J. Thrasher,
Montiel-Equihua,
Bobby Gaspar
Publication year - 2009
Publication title -
stem cells and cloning advances and applications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.606
H-Index - 22
ISSN - 1178-6957
DOI - 10.2147/sccaa.s5570
Subject(s) - adenosine deaminase deficiency , genetic enhancement , adenosine deaminase , severe combined immunodeficiency , viral vector , stem cell , hematopoietic stem cell transplantation , hematopoietic stem cell , haematopoiesis , medicine , immunodeficiency , vector (molecular biology) , gene , immunology , biology , virology , cancer research , adenosine , immune system , genetics , recombinant dna
The history of stem cell gene therapy is strongly linked to the development of gene therapy for severe combined immunodeficiencies (SCID) and especially adenosine deaminase (ADA)-deficient SCID. Here we discuss the developments achieved in over two decades of clinical and laboratory research that led to the establishment of a protocol for the autologous transplant of retroviral vector-mediated gene-modified hematopoietic stem cells, which has proved to be both successful and, to date, safe. Patients in trials in three different countries have shown long-term immunological and metabolic correction. Nevertheless, improvements to the safety profile of viral vectors are underway and will undoubtedly reinforce the position of stem cell gene therapy as a treatment option for ADA-SCID.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom