Why the study?
Does retroviral gene therapy improve immune function in preadolescents with XSCID and inadequate immune reconstitution after bone marrow transplant?
Does retroviral gene therapy improve immune function in preadolescents with XSCID and inadequate immune reconstitution after bone marrow transplant?
Retroviral gene therapy can provide multilineage marking and improve T-cell function as salvage therapy in preadolescents with XSCID.
Retroviral gene therapy can restore immunity to infants with X-linked severe combined immunodeficiency (XSCID) caused by mutations in the IL2RG gene encoding the common gamma chain (gammac) of receptors for interleukins 2 (IL-2), -4, -7, -9, -15, and -21. We investigated the safety and efficacy of gene therapy as salvage treatment for older XSCID children with inadequate immune reconstitution despite prior bone marrow transplant from a parent. Subjects received retrovirus-transduced autologous peripherally mobilized CD34(+) hematopoietic cells. T-cell function significantly improved in the youngest subject (age 10 years), and multilineage retroviral marking occurred in all 3 children.
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Chinen et al. (2007) studied this question.
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