Gene therapy improves immune function in preadolescents with X-linked severe combined immunodeficiency

Javier Chinen(National Human Genome Research Institute), Joie Davis(National Human Genome Research Institute), Suk See De Ravin(National Institutes of Health), Beverly N. Hay(National Human Genome Research Institute), Amy P. Hsu(National Human Genome Research Institute), Gilda F. Linton(National Institutes of Health), Nora Naumann(National Institutes of Health), Effie Nomicos(National Institutes of Health), Christopher Silvin(National Human Genome Research Institute), Jean Ulrick(National Institutes of Health), Narda Whiting‐Theobald(National Institutes of Health), Harry L. Malech(National Institutes of Health), Jennifer M. Puck(National Human Genome Research Institute)
Blood
March 17, 2007
Cited by 99Open Access
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Abstract

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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