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Case Reports
. 2006 Oct 24;67(8):1458-60.
doi: 10.1212/01.wnl.0000240853.97716.24. Epub 2006 Sep 13.

Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE

Affiliations
Case Reports

Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE

M Hirano et al. Neurology. .

Abstract

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is a multisystemic autosomal recessive disease due to primary thymidine phosphorylase (TP) deficiency. To restore TP activity, we performed reduced intensity allogeneic stem cell transplantations (alloSCTs) in two patients. In the first, alloSCT failed to engraft, but the second achieved mixed donor chimerism, which partially restored buffy coat TP activity and lowered plasma nucleosides. Thus, alloSCT can correct biochemical abnormalities in the blood of patients with MNGIE, but clinical efficacy remains unproven.

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Conflict of interest statement

Disclosure: The authors report no conflicts of interest.

Figures

Figure 1
Figure 1
Patient 1 pre– and post–allogeneic stem cell transplantation buffy coat thymidine phosphorylase (TP) activity in nmol/h/mg protein (A) and plasma thymidine and deoxyuridine levels in µM (B).
Figure 2
Figure 2
Patient 2 pre– and post–allogeneic stem cell transplantation buffy coat thymidine phosphorylase (TP) activity in nmol/h/mg protein (A) and plasma thymidine and deoxyuridine levels in µM (B).

Comment in

References

    1. Hirano M, Silvestri G, Blake DM, et al. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder. Neurology. 1994;44:721–727. - PubMed
    1. Nishino I, Spinazzola A, Hirano M. Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. Science. 1999;283:689–692. - PubMed
    1. Nishino I, Spinazzola A, Papadimitriou A, et al. MNGIE: an autosomal recessive disorder due to thymidine phosphorylase mutations. Ann Neurol. 2000;47:792–800. - PubMed
    1. Hirano M, Nishigaki Y, Martí R. MNGIE: a disease of two genomes. Neurologist. 2004;10:8–17. - PubMed
    1. Martí R, Nishigaki Y, Hirano M. Elevated plasma deoxyuridine in patients with thymidine phosphorylase deficiency. Biochem Biophys Res Commun. 2003;303:14–18. - PubMed

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