Literature DB >> 27362911

Pompe disease in adulthood: effects of antibody formation on enzyme replacement therapy.

Juna M de Vries1,2, Esther Kuperus1,2, Marianne Hoogeveen-Westerveld1,3, Marian A Kroos1,3, Stephan C A Wens1,2, Merel Stok1,3,4, Nadine A M E van der Beek1,2, Michelle E Kruijshaar1,4, Dimitris Rizopoulos5, Pieter A van Doorn1,2, Ans T van der Ploeg1,4, W W M Pim Pijnappel1,3,4.   

Abstract

PURPOSE: To determine the effect of antibodies against recombinant human acid α-glucosidase (rhGAA) on treatment efficacy and safety, and to test whether the GAA genotype is involved in antibody formation.
METHODS: We used enzyme-linked immunosorbent assay (ELISA) to determine anti-rhGAA antibody titers at baseline and at 6, 12, and 36 months of rhGAA treatment. We measured the capacity of antibodies to neutralize rhGAA enzymatic activity or cellular uptake and the effects on infusion-associated reactions (IARs), muscle strength, and pulmonary function.
RESULTS: Of 73 patients, 45 developed antibodies. Maximal titers were high (≥1:31,250) in 22% of patients, intermediate (1:1,250-1:31,250) in 40%, and none or low (0-1:1,250) in 38%. The common IVS1/delex18 GAA genotype was absent only in the high-titer group. The height of the titer positively correlated with the occurrence and number of IARs (P ≤ 0.001). On the group level, antibody titers did not correlate with treatment efficacy. Eight patients (11%) developed very high maximal titers (≥156,250), but only one patient showed high sustained neutralizing antibodies that probably interfered with treatment efficacy.
CONCLUSIONS: In adults with Pompe disease, antibody formation does not interfere with rhGAA efficacy in the majority of patients, is associated with IARs, and may be attenuated by the IVS1/delex18 GAA genotype.Genet Med 19 1, 90-97.

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Year:  2016        PMID: 27362911     DOI: 10.1038/gim.2016.70

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  35 in total

1.  Broad spectrum of Pompe disease in patients with the same c.-32-13T->G haplotype.

Authors:  M A Kroos; R J Pomponio; M L Hagemans; J L M Keulemans; M Phipps; M DeRiso; R E Palmer; M G E M Ausems; N A M E Van der Beek; O P Van Diggelen; D J J Halley; A T Van der Ploeg; A J J Reuser
Journal:  Neurology       Date:  2007-01-09       Impact factor: 9.910

2.  Long-term observational, non-randomized study of enzyme replacement therapy in late-onset glycogenosis type II.

Authors:  Bruno Bembi; Federica Edith Pisa; Marco Confalonieri; Giovanni Ciana; Agata Fiumara; Rossella Parini; Miriam Rigoldi; Arrigo Moglia; Alfredo Costa; Annalisa Carlucci; Cesare Danesino; Maria Gabriela Pittis; Andrea Dardis; Sabrina Ravaglia
Journal:  J Inherit Metab Dis       Date:  2010-09-14       Impact factor: 4.982

3.  Anti-α-galactosidase A antibody response to agalsidase beta treatment: data from the Fabry Registry.

Authors:  William R Wilcox; Gabor E Linthorst; Dominique P Germain; Ulla Feldt-Rasmussen; Stephen Waldek; Susan M Richards; Dana Beitner-Johnson; Marta Cizmarik; J Alexander Cole; Wytske Kingma; David G Warnock
Journal:  Mol Genet Metab       Date:  2011-12-14       Impact factor: 4.797

4.  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

5.  B-Cell depletion and immunomodulation before initiation of enzyme replacement therapy blocks the immune response to acid alpha-glucosidase in infantile-onset Pompe disease.

Authors:  Melissa E Elder; Sushrusha Nayak; Shelley W Collins; Lee Ann Lawson; Jeffry S Kelley; Roland W Herzog; Renee F Modica; Judy Lew; Robert M Lawrence; Barry J Byrne
Journal:  J Pediatr       Date:  2013-04-16       Impact factor: 4.406

Review 6.  Pompe's disease.

Authors:  Ans T van der Ploeg; Arnold J J Reuser
Journal:  Lancet       Date:  2008-10-11       Impact factor: 79.321

7.  Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I.

Authors:  Lorne A Clarke; J Edmond Wraith; Michael Beck; Edwin H Kolodny; Gregory M Pastores; Joseph Muenzer; David M Rapoport; Kenneth I Berger; Marisa Sidman; Emil D Kakkis; Gerald F Cox
Journal:  Pediatrics       Date:  2009-01       Impact factor: 7.124

8.  The impact of antibodies on clinical outcomes in diseases treated with therapeutic protein: lessons learned from infantile Pompe disease.

Authors:  Suhrad G Banugaria; Sean N Prater; Yiu-Ki Ng; Joyce A Kobori; Richard S Finkel; Roger L Ladda; Yuan-Tsong Chen; Amy S Rosenberg; Priya S Kishnani
Journal:  Genet Med       Date:  2011-08       Impact factor: 8.822

9.  Enzyme therapy and immune response in relation to CRIM status: the Dutch experience in classic infantile Pompe disease.

Authors:  Carin M van Gelder; Marianne Hoogeveen-Westerveld; Marian A Kroos; Iris Plug; Ans T van der Ploeg; Arnold J J Reuser
Journal:  J Inherit Metab Dis       Date:  2014-04-09       Impact factor: 4.982

10.  Mucopolysaccharidosis type VI phenotypes-genotypes and antibody response to galsulfase.

Authors:  Marion M Brands; Marianne Hoogeveen-Westerveld; Marian A Kroos; Willemieke Nobel; George J Ruijter; Lale Özkan; Iris Plug; Daniel Grinberg; Lluïsa Vilageliu; Dicky J Halley; Ans T van der Ploeg; Arnold J Reuser
Journal:  Orphanet J Rare Dis       Date:  2013-04-04       Impact factor: 4.123

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  16 in total

Review 1.  Challenges in treating Pompe disease: an industry perspective.

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

Review 2.  Immunological challenges and approaches to immunomodulation in Pompe disease: a literature review.

Authors:  Ankit K Desai; Cindy Li; Amy S Rosenberg; Priya S Kishnani
Journal:  Ann Transl Med       Date:  2019-07

3.  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

Review 4.  Engineered skeletal muscles for disease modeling and drug discovery.

Authors:  Jason Wang; Alastair Khodabukus; Lingjun Rao; Keith Vandusen; Nadia Abutaleb; Nenad Bursac
Journal:  Biomaterials       Date:  2019-08-08       Impact factor: 12.479

5.  Response to de Vries et al.

Authors:  Mrudu Herbert; Zoheb B Kazi; Susan Richards; Amy S Rosenberg; Priya S Kishnani
Journal:  Genet Med       Date:  2017-05-11       Impact factor: 8.822

6.  Response to Herbert et al.

Authors:  Juna M de Vries; Esther Kuperus; Marianne Hoogeveen-Westerveld; Marian A Kroos; Stephan C A Wens; Merel Stok; Nadine A M E van der Beek; Michelle E Kruijshaar; Dimitris Rizopoulos; Pieter A van Doorn; Ans T van der Ploeg; W W M Pim Pijnappel
Journal:  Genet Med       Date:  2017-06-29       Impact factor: 8.822

7.  The ACE I/D polymorphism does not explain heterogeneity of natural course and response to enzyme replacement therapy in Pompe disease.

Authors:  Esther Kuperus; Jan C van der Meijden; Stijn L M In 't Groen; Marian A Kroos; Marianne Hoogeveen-Westerveld; Dimitris Rizopoulos; Monica Yasmin Nino Martinez; Michelle E Kruijshaar; Pieter A van Doorn; Nadine A M E van der Beek; Ans T van der Ploeg; W W M Pim Pijnappel
Journal:  PLoS One       Date:  2018-12-07       Impact factor: 3.240

8.  Effects of immunomodulation in classic infantile Pompe patients with high antibody titers.

Authors:  E Poelman; M Hoogeveen-Westerveld; J M P van den Hout; R G M Bredius; A C Lankester; G J A Driessen; S S M Kamphuis; W W M Pijnappel; A T van der Ploeg
Journal:  Orphanet J Rare Dis       Date:  2019-03-22       Impact factor: 4.123

9.  Long-Term Observation of the Safety and Effectiveness of Enzyme Replacement Therapy in Japanese Patients with Pompe Disease: Results From the Post-marketing Surveillance.

Authors:  Hitoshi Nagura; Jiro Hokugo; Kazuo Ueda
Journal:  Neurol Ther       Date:  2019-09-26

10.  Long-term follow-up of 17 patients with childhood Pompe disease treated with enzyme replacement therapy.

Authors:  Jan C van der Meijden; Michelle E Kruijshaar; Laurike Harlaar; Dimitris Rizopoulos; Nadine A M E van der Beek; Ans T van der Ploeg
Journal:  J Inherit Metab Dis       Date:  2018-03-19       Impact factor: 4.982

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