Literature DB >> 25052852

A chaperone enhances blood α-glucosidase activity in Pompe disease patients treated with enzyme replacement therapy.

Giancarlo Parenti1, Simona Fecarotta2, Giancarlo la Marca3, Barbara Rossi4, Serena Ascione2, Maria Alice Donati5, Lucia Ovidia Morandi6, Sabrina Ravaglia7, Anna Pichiecchio7, Daniela Ombrone3, Michele Sacchini5, Maria Barbara Pasanisi6, Paola De Filippi8, Cesare Danesino8, Roberto Della Casa2, Alfonso Romano2, Carmine Mollica9, Margherita Rosa2, Teresa Agovino2, Edoardo Nusco4, Caterina Porto1, Generoso Andria2.   

Abstract

Enzyme replacement therapy is currently the only approved treatment for Pompe disease, due to acid α-glucosidase deficiency. Clinical efficacy of this approach is variable, and more effective therapies are needed. We showed in preclinical studies that chaperones stabilize the recombinant enzyme used for enzyme replacement therapy. Here, we evaluated the effects of a combination of enzyme therapy and a chaperone on α-glucosidase activity in Pompe disease patients. α-Glucosidase activity was analyzed by tandem-mass spectrometry in dried blood spots from patients treated with enzyme replacement therapy, either alone or in combination with the chaperone N-butyldeoxynojirimycin given at the time of the enzyme infusion. Thirteen patients with different presentations (3 infantile-onset, 10 late-onset) were enrolled. In 11 patients, the combination treatment resulted in α-glucosidase activities greater than 1.85-fold the activities with enzyme replacement therapy alone. In the whole patient population, α-glucosidase activity was significantly increased at 12 hours (2.19-fold, P = 0.002), 24 hours (6.07-fold, P = 0.001), and 36 hours (3.95-fold, P = 0.003). The areas under the curve were also significantly increased (6.78-fold, P = 0.002). These results suggest improved stability of recombinant α-glucosidase in blood in the presence of the chaperone.

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Year:  2014        PMID: 25052852      PMCID: PMC4429731          DOI: 10.1038/mt.2014.138

Source DB:  PubMed          Journal:  Mol Ther        ISSN: 1525-0016            Impact factor:   11.454


  38 in total

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3.  Liquid chromatographic assay for a glucose tetrasaccharide, a putative biomarker for the diagnosis of Pompe disease.

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Journal:  Anal Biochem       Date:  2000-12-01       Impact factor: 3.365

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9.  Targeted disruption of the acid alpha-glucosidase gene in mice causes an illness with critical features of both infantile and adult human glycogen storage disease type II.

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Authors:  Giancarlo Parenti; Alfredo Zuppaldi; M Gabriela Pittis; M Rosaria Tuzzi; Ida Annunziata; Germana Meroni; Caterina Porto; Francesca Donaudy; Barbara Rossi; Massimiliano Rossi; Mirella Filocamo; Alice Donati; Bruno Bembi; Andrea Ballabio; Generoso Andria
Journal:  Mol Ther       Date:  2007-01-09       Impact factor: 11.454

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  29 in total

Review 1.  Genetic neuromuscular disorders: living the era of a therapeutic revolution. Part 2: diseases of motor neuron and skeletal muscle.

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Journal:  Neurol Sci       Date:  2019-02-25       Impact factor: 3.307

Review 2.  Challenges in treating Pompe disease: an industry perspective.

Authors:  Hung V Do; Richie Khanna; Russell Gotschall
Journal:  Ann Transl Med       Date:  2019-07

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Authors:  Lara Kohler; Rosa Puertollano; Nina Raben
Journal:  Neurotherapeutics       Date:  2018-10       Impact factor: 7.620

Review 4.  Small molecules as therapeutic agents for inborn errors of metabolism.

Authors:  Leslie Matalonga; Laura Gort; Antonia Ribes
Journal:  J Inherit Metab Dis       Date:  2016-12-13       Impact factor: 4.982

5.  Rescue of Pompe disease in mice by AAV-mediated liver delivery of secretable acid α-glucosidase.

Authors:  Francesco Puzzo; Pasqualina Colella; Maria G Biferi; Deeksha Bali; Nicole K Paulk; Patrice Vidal; Fanny Collaud; Marcelo Simon-Sola; Severine Charles; Romain Hardet; Christian Leborgne; Amine Meliani; Mathilde Cohen-Tannoudji; Stephanie Astord; Bernard Gjata; Pauline Sellier; Laetitia van Wittenberghe; Alban Vignaud; Florence Boisgerault; Martine Barkats; Pascal Laforet; Mark A Kay; Dwight D Koeberl; Giuseppe Ronzitti; Federico Mingozzi
Journal:  Sci Transl Med       Date:  2017-11-29       Impact factor: 17.956

6.  Improved efficacy of a next-generation ERT in murine Pompe disease.

Authors:  Su Xu; Yi Lun; Michelle Frascella; Anadina Garcia; Rebecca Soska; Anju Nair; Abdul S Ponery; Adriane Schilling; Jessie Feng; Steven Tuske; Maria Cecilia Della Valle; José A Martina; Evelyn Ralston; Russell Gotschall; Kenneth J Valenzano; Rosa Puertollano; Hung V Do; Nina Raben; Richie Khanna
Journal:  JCI Insight       Date:  2019-03-07

7.  Correcting Neuromuscular Deficits With Gene Therapy in Pompe Disease.

Authors:  Adrian G Todd; Jessica A McElroy; Robert W Grange; David D Fuller; Glenn A Walter; Barry J Byrne; Darin J Falk
Journal:  Ann Neurol       Date:  2015-06-30       Impact factor: 10.422

8.  In Vitro Enzyme Measurement to Test Pharmacological Chaperone Responsiveness in Fabry and Pompe Disease.

Authors:  Jan Lukas; Anne-Marie Knospe; Susanne Seemann; Valentina Citro; Maria V Cubellis; Arndt Rolfs
Journal:  J Vis Exp       Date:  2017-12-20       Impact factor: 1.355

Review 9.  Progress and challenges of gene therapy for Pompe disease.

Authors:  Giuseppe Ronzitti; Fanny Collaud; Pascal Laforet; Federico Mingozzi
Journal:  Ann Transl Med       Date:  2019-07

Review 10.  [Innovative therapeutic approaches for hereditary neuromuscular diseases].

Authors:  J Kirschner; B Schoser
Journal:  Nervenarzt       Date:  2018-10       Impact factor: 1.214

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