Literature DB >> 22371174

Hematopoietic stem cell transplantation improves the high incidence of neutralizing allo-antibodies observed in Hurler's syndrome after pharmacological enzyme replacement therapy.

Muhammad Ameer Saif1, Brian W Bigger, Karen E Brookes, Jean Mercer, Karen L Tylee, Heather J Church, Denise K Bonney, Simon Jones, J Ed Wraith, Robert F Wynn.   

Abstract

BACKGROUND: Mucopolysaccharidosis type I is caused by deficiency of α-L-iduronidase. Currently available treatment options include an allogeneic hematopoietic stem cell transplant and enzyme replacement therapy. Exogenous enzyme therapy appears promising but the benefits may be attenuated, at least in some patients, by the development of an immune response to the delivered enzyme. The incidence and impact of alloimmune responses in these patients remain unknown. DESIGN AND METHODS: We developed an immunoglobulin G enzyme-linked immunosorbent assay as well as in vitro catalytic enzyme inhibition and cellular uptake inhibition assays and quantified enzyme inhibition by allo-antibodies. We determined the impact of these antibodies in eight patients who received enzyme therapy before and during hematopoietic stem cell transplantation. In addition, 20 patients who had previously received an allogeneic stem cell transplant were tested to evaluate this treatment as an immune tolerance induction mechanism.
RESULTS: High titer immune responses were seen in 87.5% (7/8) patients following exposure to α-L-iduronidase. These patients exhibited catalytic enzyme inhibition (5/8), uptake inhibition of catalytically active enzyme (6/8) or both (4/8). High antibody titers generally preceded elevation of previously described biomarkers of disease progression. The median time to development of immune tolerance was 101 days (range, 26-137) after transplantation. All 20 patients, including those with mixed chimerism (22%), tested 1 year after transplantation were tolerized despite normal enzyme levels.
CONCLUSIONS: We found a high incidence of neutralizing antibodies in patients with mucopolysaccharidosis type I treated with enzyme replacement therapy. We also found that allogeneic hematopoietic stem cell transplantation was an effective and rapid immune tolerance induction strategy.

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Year:  2012        PMID: 22371174      PMCID: PMC3436232          DOI: 10.3324/haematol.2011.058644

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  36 in total

1.  High antibody titer in an adult with Pompe disease affects treatment with alglucosidase alfa.

Authors:  Juna M de Vries; Nadine A M E van der Beek; Marian A Kroos; Lale Ozkan; Pieter A van Doorn; Susan M Richards; Crystal C C Sung; Jan-Dietert C Brugma; Adrienne A M Zandbergen; Ans T van der Ploeg; Arnold J J Reuser
Journal:  Mol Genet Metab       Date:  2010-08-14       Impact factor: 4.797

2.  Cross-reactive immunologic material status affects treatment outcomes in Pompe disease infants.

Authors:  Priya S Kishnani; Paula C Goldenberg; Stephanie L DeArmey; James Heller; Danny Benjamin; Sarah Young; Deeksha Bali; Sue Ann Smith; Jennifer S Li; Hanna Mandel; Dwight Koeberl; Amy Rosenberg; Y-T Chen
Journal:  Mol Genet Metab       Date:  2010-01       Impact factor: 4.797

3.  Use of enzyme replacement therapy (Laronidase) before hematopoietic stem cell transplantation for mucopolysaccharidosis I: experience in 18 patients.

Authors:  Robert F Wynn; Jean Mercer; Joanne Page; Trevor F Carr; Simon Jones; J Edmond Wraith
Journal:  J Pediatr       Date:  2009-01       Impact factor: 4.406

4.  Evaluation of heparin cofactor II-thrombin complex as a biomarker on blood spots from mucopolysaccharidosis I, IIIA and IIIB mice.

Authors:  Kia Langford-Smith; Malani Arasaradnam; J Ed Wraith; Rob Wynn; Brian W Bigger
Journal:  Mol Genet Metab       Date:  2009-10-23       Impact factor: 4.797

5.  Partial phenotypic correction and immune tolerance induction to enzyme replacement therapy after hematopoietic stem cell gene transfer of alpha-glucosidase in Pompe disease.

Authors:  Gaëlle Douillard-Guilloux; Emmanuel Richard; Lionel Batista; Catherine Caillaud
Journal:  J Gene Med       Date:  2009-04       Impact factor: 4.565

Review 6.  Hematopoietic cell transplantation for autoimmune disease: updates from Europe and the United States.

Authors:  Keith M Sullivan; Paolo Muraro; Alan Tyndall
Journal:  Biol Blood Marrow Transplant       Date:  2009-11-04       Impact factor: 5.742

7.  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
Journal:  J Pediatr       Date:  2009-04       Impact factor: 4.406

8.  Immune tolerance improves the efficacy of enzyme replacement therapy in canine mucopolysaccharidosis I.

Authors:  Patricia Dickson; Maryn Peinovich; Michael McEntee; Thomas Lester; Steven Le; Aimee Krieger; Hayden Manuel; Catherine Jabagat; Merry Passage; Emil D Kakkis
Journal:  J Clin Invest       Date:  2008-08       Impact factor: 14.808

9.  Immune response hinders therapy for lysosomal storage diseases.

Authors:  Katherine P Ponder
Journal:  J Clin Invest       Date:  2008-08       Impact factor: 14.808

10.  Heparin cofactor II-thrombin complex and dermatan sulphate:chondroitin sulphate ratio are biomarkers of short- and long-term treatment effects in mucopolysaccharide diseases.

Authors:  Kia Jane Langford-Smith; Jean Mercer; June Petty; Karen Tylee; Heather Church; Jane Roberts; Gill Moss; Simon Jones; Rob Wynn; J Ed Wraith; Brian W Bigger
Journal:  J Inherit Metab Dis       Date:  2010-12-18       Impact factor: 4.982

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  20 in total

Review 1.  Hematopoietic Stem Cell Transplantation for Mucopolysaccharidoses: Past, Present, and Future.

Authors:  Madeleine Taylor; Shaukat Khan; Molly Stapleton; Jianmin Wang; Jing Chen; Robert Wynn; Hiromasa Yabe; Yasutsugu Chinen; Jaap Jan Boelens; Robert W Mason; Francyne Kubaski; Dafne D G Horovitz; Anneliese L Barth; Marta Serafini; Maria Ester Bernardo; Hironori Kobayashi; Kenji E Orii; Yasuyuki Suzuki; Tadao Orii; Shunji Tomatsu
Journal:  Biol Blood Marrow Transplant       Date:  2019-02-14       Impact factor: 5.742

2.  Plasma and urinary levels of dermatan sulfate and heparan sulfate derived disaccharides after long-term enzyme replacement therapy (ERT) in MPS I: correlation with the timing of ERT and with total urinary excretion of glycosaminoglycans.

Authors:  Minke H de Ru; Linda van der Tol; Naomi van Vlies; Brian W Bigger; Carla E M Hollak; Lodewijk Ijlst; Wim Kulik; Henk van Lenthe; Muhammad A Saif; Tom Wagemans; Willem M van der Wal; Ronald J Wanders; Frits A Wijburg
Journal:  J Inherit Metab Dis       Date:  2012-09-19       Impact factor: 4.982

3.  Management of mucopolysaccharidosis type IH (Hurler's syndrome) presenting in infancy with severe dilated cardiomyopathy: a single institution's experience.

Authors:  Daniel H Wiseman; Jean Mercer; Karen Tylee; Nilima Malaiya; Denise K Bonney; Simon A Jones; J Edmond Wraith; Robert F Wynn
Journal:  J Inherit Metab Dis       Date:  2012-06-21       Impact factor: 4.982

4.  Hematopoietic stem cell and gene therapy corrects primary neuropathology and behavior in mucopolysaccharidosis IIIA mice.

Authors:  Alexander Langford-Smith; Fiona L Wilkinson; Kia J Langford-Smith; Rebecca J Holley; Ana Sergijenko; Steven J Howe; William R Bennett; Simon A Jones; Je Wraith; Catherine Lr Merry; Robert F Wynn; Brian W Bigger
Journal:  Mol Ther       Date:  2012-05-01       Impact factor: 11.454

Review 5.  The impact of the immune system on the safety and efficiency of enzyme replacement therapy in lysosomal storage disorders.

Authors:  A Broomfield; S A Jones; S M Hughes; B W Bigger
Journal:  J Inherit Metab Dis       Date:  2016-02-16       Impact factor: 4.982

6.  Hematopoietic Stem Cell Transplantation for Patients with Mucopolysaccharidosis II.

Authors:  Francyne Kubaski; Hiromasa Yabe; Yasuyuki Suzuki; Toshiyuki Seto; Takashi Hamazaki; Robert W Mason; Li Xie; Tor Gunnar Hugo Onsten; Sandra Leistner-Segal; Roberto Giugliani; Vũ Chí Dũng; Can Thi Bich Ngoc; Seiji Yamaguchi; Adriana M Montaño; Kenji E Orii; Toshiyuki Fukao; Haruo Shintaku; Tadao Orii; Shunji Tomatsu
Journal:  Biol Blood Marrow Transplant       Date:  2017-07-01       Impact factor: 5.742

7.  Enzyme replacement therapy prior to haematopoietic stem cell transplantation in Mucopolysaccharidosis Type I: 10 year combined experience of 2 centres.

Authors:  Arunabha Ghosh; Weston Miller; Paul J Orchard; Simon A Jones; Jean Mercer; Heather J Church; Karen Tylee; Troy Lund; Brian W Bigger; Jakub Tolar; Robert F Wynn
Journal:  Mol Genet Metab       Date:  2016-01-27       Impact factor: 4.797

Review 8.  Therapeutic Options for Mucopolysaccharidoses: Current and Emerging Treatments.

Authors:  Kazuki Sawamoto; Molly Stapleton; Carlos J Alméciga-Díaz; Angela J Espejo-Mojica; Juan Camilo Losada; Diego A Suarez; Shunji Tomatsu
Journal:  Drugs       Date:  2019-07       Impact factor: 11.431

9.  Sleep disordered breathing in mucopolysaccharidosis I: a multivariate analysis of patient, therapeutic and metabolic correlators modifying long term clinical outcome.

Authors:  Abhijit Ricky Pal; Eveline J Langereis; Muhammad A Saif; Jean Mercer; Heather J Church; Karen L Tylee; Robert F Wynn; Frits A Wijburg; Simon A Jones; Iain A Bruce; Brian W Bigger
Journal:  Orphanet J Rare Dis       Date:  2015-04-10       Impact factor: 4.123

10.  Myeloid/Microglial driven autologous hematopoietic stem cell gene therapy corrects a neuronopathic lysosomal disease.

Authors:  Ana Sergijenko; Alexander Langford-Smith; Ai Y Liao; Claire E Pickford; John McDermott; Gabriel Nowinski; Kia J Langford-Smith; Catherine L R Merry; Simon A Jones; J Edmond Wraith; Robert F Wynn; Fiona L Wilkinson; Brian W Bigger
Journal:  Mol Ther       Date:  2013-06-07       Impact factor: 11.454

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