Table 6.

X-linked severe combined immunodeficiency as a candidate disease for gene therapy.

*Data from Kohn et al23; A. Fischer and M. Cavazzana-Calvo, personal communication in oral presentations, 2003 
Advantages 
    Complications and late failures after allogeneic transplantation mandate a search for better treatment. 
    Ex-vivo transduction: hematopoietic cells can be removed and enriched, cultured with retrovirus and then reinfused intravenously, where they will home to the bone marrow. 
    Disease gene product, the common gamma chain of cytokine receptors is widely expressed in blood lineages; overexpression apparently not harmful. 
    The problem of immune elimination of the corrected cells should not arise because of the immunodeficiency phenotype. 
    There is an in vivo selective advantage for lymphoid cells expressing the normal common gamma chain protein. 
    Animal models and human trials have been successful in restoring immunocompetence. 
    Of 10 infants given gene therapy as primary treatment in France by the group of Fischer et al, 9 had restoration of T-cell function.31,32  
    Specific antibody production was restored in most. 
    A dose of > 1 million corrected CD34+ cells/kg was established as required to achieve full reconstitution. 
Disadvantages
    Serious adverse events occurred in 2/10 infants: development of clonal leukemic proliferations of transduced cells. 
    Both were the youngest infants at treatment (1 and 3 months). 
    Clonal proliferations were detected about 2½ years after gene therapy. 
    The patients’ leukemic clones had different retroviral insertion sites, but both were near the 5′ end of the LIM domain only LMO-2 transcription factor gene. 
    Both patients have required chemotherapy, and the first received an allogeneic stem cell transplant. 
    Retrovirus vectors, chosen for their ability to effect permanent correction by integrating into the host chromosomal DNA, do not permit control of insertion site. 
    Possible harmful interactions between endogenous host factors (age, disease-specific effects, other inherited susceptibility genes, infections) and host genes whose expression is altered by nearby retroviral insertion (transcription factors, such as LMO-2) can combine to produce leukemia. 
*Data from Kohn et al23; A. Fischer and M. Cavazzana-Calvo, personal communication in oral presentations, 2003 
Advantages 
    Complications and late failures after allogeneic transplantation mandate a search for better treatment. 
    Ex-vivo transduction: hematopoietic cells can be removed and enriched, cultured with retrovirus and then reinfused intravenously, where they will home to the bone marrow. 
    Disease gene product, the common gamma chain of cytokine receptors is widely expressed in blood lineages; overexpression apparently not harmful. 
    The problem of immune elimination of the corrected cells should not arise because of the immunodeficiency phenotype. 
    There is an in vivo selective advantage for lymphoid cells expressing the normal common gamma chain protein. 
    Animal models and human trials have been successful in restoring immunocompetence. 
    Of 10 infants given gene therapy as primary treatment in France by the group of Fischer et al, 9 had restoration of T-cell function.31,32  
    Specific antibody production was restored in most. 
    A dose of > 1 million corrected CD34+ cells/kg was established as required to achieve full reconstitution. 
Disadvantages
    Serious adverse events occurred in 2/10 infants: development of clonal leukemic proliferations of transduced cells. 
    Both were the youngest infants at treatment (1 and 3 months). 
    Clonal proliferations were detected about 2½ years after gene therapy. 
    The patients’ leukemic clones had different retroviral insertion sites, but both were near the 5′ end of the LIM domain only LMO-2 transcription factor gene. 
    Both patients have required chemotherapy, and the first received an allogeneic stem cell transplant. 
    Retrovirus vectors, chosen for their ability to effect permanent correction by integrating into the host chromosomal DNA, do not permit control of insertion site. 
    Possible harmful interactions between endogenous host factors (age, disease-specific effects, other inherited susceptibility genes, infections) and host genes whose expression is altered by nearby retroviral insertion (transcription factors, such as LMO-2) can combine to produce leukemia. 

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