Literature DB >> 23430937

Cross correction following haemopoietic stem cell transplant for purine nucleoside phosphorylase deficiency: engrafted donor-derived white blood cells provide enzyme to residual enzyme-deficient recipient cells.

Vikramajit Singh1.   

Abstract

Purine nucleoside phosphorylase (PNP) deficiency is an immunodeficiency disorder characterized by recurrent infections, failure to thrive and neurologic symptomatology. While enzyme replacement therapy (ERT) is a therapeutic option for adenine deaminase (ADA) deficiency, a similar disorder, this is not available for PNP deficiency, and bone marrow transplant (BMT) is the only treatment option. Moreover, even with BMT, improvement of neurological deficits is not definite. We describe a 16-month-old boy who underwent BMT for PNP deficiency which resulted not only in freedom from infections but also in neurological improvement and autologous T-cell recovery.Pre-transplant, this child had severe lymphopenia with recurrent infections and psychomotor retardation. Post-transplant, in the presence of mixed chimerism, he had normal lymphocyte count, including presence of recipient T cells and neurological improvement. The re-emergence of recipient T cells, when there were virtually no such cells pre-transplant, and the neurological improvement are indicative of improvement of the enzyme deficiency in tissues which remain genetically enzyme depleted.These defects are not directly corrected by BMT, but are due to delivery of the missing enzyme by the transplanted tissue. In this aspect, transplantation in PNP deficiency is similar to transplantation in other inborn errors of metabolism where the engrafted donor cells deliver enzyme and restore function to deficient tissues. This further lends support to the recommendations that BMT should be the favoured treatment option in disorders like ADA deficiency or Hurler syndrome, where, even though ERT is available, it is limited by inability to correct the central nervous system defects.

Entities:  

Year:  2012        PMID: 23430937      PMCID: PMC3565632          DOI: 10.1007/8904_2012_126

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  9 in total

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Authors:  J Priller; A Flügel; T Wehner; M Boentert; C A Haas; M Prinz; F Fernández-Klett; K Prass; I Bechmann; B A de Boer; M Frotscher; G W Kreutzberg; D A Persons; U Dirnagl
Journal:  Nat Med       Date:  2001-12       Impact factor: 53.440

2.  Allogeneic bone marrow transplantation for lysosomal storage diseases. The European Group for Bone Marrow Transplantation.

Authors:  P M Hoogerbrugge; O F Brouwer; P Bordigoni; O Ringden; P Kapaun; J J Ortega; A O'Meara; G Cornu; G Souillet; D Frappaz
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Review 3.  Enzyme replacement and enhancement therapies: lessons from lysosomal disorders.

Authors:  Robert J Desnick; Edward H Schuchman
Journal:  Nat Rev Genet       Date:  2002-12       Impact factor: 53.242

4.  Purine nucleoside phosphorylase deficiency (PNP-def) presenting with lymphopenia and developmental delay: successful correction with umbilical cord blood transplantation.

Authors:  Laurie A Myers; Michael S Hershfield; Wirt T Neale; Maria Escolar; Joanne Kurtzberg
Journal:  J Pediatr       Date:  2004-11       Impact factor: 4.406

5.  Improved metabolic correction in patients with lysosomal storage disease treated with hematopoietic stem cell transplant compared with enzyme replacement therapy.

Authors:  Robert F Wynn; J Ed Wraith; Jean Mercer; Anne O'Meara; Karen Tylee; Margaret Thornley; Heather J Church; Brian W Bigger
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6.  Human CD34+ cells differentiate into microglia and express recombinant therapeutic protein.

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Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-27       Impact factor: 11.205

Review 7.  PEG-ADA: an alternative to haploidentical bone marrow transplantation and an adjunct to gene therapy for adenosine deaminase deficiency.

Authors:  M S Hershfield
Journal:  Hum Mutat       Date:  1995       Impact factor: 4.878

8.  Enzyme replacement therapy and/or hematopoietic stem cell transplantation at diagnosis in patients with mucopolysaccharidosis type I: results of a European consensus procedure.

Authors:  Minke H de Ru; Jaap J Boelens; Anibh M Das; Simon A Jones; Johanna H van der Lee; Nizar Mahlaoui; Eugen Mengel; Martin Offringa; Anne O'Meara; Rossella Parini; Attilio Rovelli; Karl-Walter Sykora; Vassili Valayannopoulos; Ashok Vellodi; Robert F Wynn; Frits A Wijburg
Journal:  Orphanet J Rare Dis       Date:  2011-08-10       Impact factor: 4.123

9.  Pegademase bovine (PEG-ADA) for the treatment of infants and children with severe combined immunodeficiency (SCID).

Authors:  Claire Booth; H Bobby Gaspar
Journal:  Biologics       Date:  2009-07-13
  9 in total
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1.  Hematopoietic cell transplantation for a child with OSTM1 osteopetrosis.

Authors:  Kathleen M Overholt; Melissa J Rose; Sarita Joshi; Gail E Herman; Rajinder Bajwa; Rolla Abu-Arja; Hemalatha G Rangarajan; Edwin M Horwitz
Journal:  Blood Adv       Date:  2016-12-30

2.  Novel Genetic Mutations in the First Swedish Patient with Purine Nucleoside Phosphorylase Deficiency and Clinical Outcome After Hematopoietic Stem Cell Transplantation with HLA-Matched Unrelated Donor.

Authors:  Nicholas Brodszki; Maria Svensson; André B P van Kuilenburg; Judith Meijer; Lida Zoetekouw; Lennart Truedsson; Jacek Toporski
Journal:  JIMD Rep       Date:  2015-05-13

3.  Upfront Enzyme Replacement via Erythrocyte Transfusions for PNP Deficiency.

Authors:  Anna Eichinger; Horst von Bernuth; Michael H Albert; Fabian Hauck; Cinzia Dedieu; Sebastian A Schroeder; Giancarlo la Marca
Journal:  J Clin Immunol       Date:  2021-02-27       Impact factor: 8.317

4.  The Broad Clinical Spectrum and Transplant Results of PNP Deficiency.

Authors:  Polina Stepensky; Irina Zaidman; Yael Dinur Schejter; Ehud Even-Or; Bella Shadur; Adeeb NaserEddin
Journal:  J Clin Immunol       Date:  2019-11-09       Impact factor: 8.542

  4 in total

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