Retroviral-mediated transfer and expression of the common gamma chain into human hematopoietic progenitors

被引:0
|
作者
Candotti, F [1 ]
Onodera, M [1 ]
Knazek, RA [1 ]
Blaese, RM [1 ]
机构
[1] NHGRI, Clin Gene Therapy Branch, NIH, Bethesda, MD 20892 USA
关键词
gene therapy; hematopoietic progenitors; retroviral vectors; XSCID;
D O I
10.1159/000040932
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The common gamma chain (gamma(c)) of cytokine receptors is mutated in X-linked severe combined immunodeficiency, a lethal disorder characterized by the absence of both humoral and cellular immune defenses, Allogeneic bone marrow transplantation from HLA-identical siblings usually results in complete reconstitution of the immune system and is the current treatment of choice. Genetic correction and reinfusion of autologous hematopoietic stem cells represents an alternative therapeutic approach for those patients who lack suitable marrow donors. In this study, we show that retroviral-mediated transfer of the gamma(c) gene results in efficient expression in CD34+ cells and high transduction rate of colony-forming progenitors.
引用
收藏
页码:106 / 110
页数:5
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