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Published in: Journal of Inherited Metabolic Disease 1/2011

Open Access 01-02-2011 | Letter to the Editors

Letter concerning “Enzyme replacement therapy in a patient with Fabry disease and the development of IgE antibodies against agalsidase beta but not agalsidase alpha”, by Tanaka et al.

Authors: Gabor E. Linthorst, Johannes M. F. G. Aerts

Published in: Journal of Inherited Metabolic Disease | Issue 1/2011

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Excerpt

Dear editor, …
Literature
go back to reference Linthorst GE, Hollak CEM, Donker-Koopman WE, Strijland A, Aerts JMFG (2004) Enzyme therapy for Fabry disease: Neutralizing antibodies toward agalsidase alpha and beta. Kidney International 66(4):1589–1595CrossRefPubMed Linthorst GE, Hollak CEM, Donker-Koopman WE, Strijland A, Aerts JMFG (2004) Enzyme therapy for Fabry disease: Neutralizing antibodies toward agalsidase alpha and beta. Kidney International 66(4):1589–1595CrossRefPubMed
go back to reference Linthorst GE, Vedder AC, Ormel EE, Aerts JM, Hollak CE (2006) Home treatment for Fabry disease: practice guidelines based on 3 years experience in The Netherlands. Nephrology, Dialysis, Transplantation 21(2):355–360CrossRefPubMed Linthorst GE, Vedder AC, Ormel EE, Aerts JM, Hollak CE (2006) Home treatment for Fabry disease: practice guidelines based on 3 years experience in The Netherlands. Nephrology, Dialysis, Transplantation 21(2):355–360CrossRefPubMed
go back to reference Ohashi T, Sakuma M, Kitagawa T, Suzuki K, Ishige N, Eto Y (2007) Influence of antibody formation on reduction of globotriaosylceramide (GL-3) in urine from Fabry patients during agalsidase beta therapy. MolGenetMetab 92(3):271–273 Ohashi T, Sakuma M, Kitagawa T, Suzuki K, Ishige N, Eto Y (2007) Influence of antibody formation on reduction of globotriaosylceramide (GL-3) in urine from Fabry patients during agalsidase beta therapy. MolGenetMetab 92(3):271–273
go back to reference Schellekens H (2008) The immunogenicity of therapeutic proteins and the Fabry antibody standardization initiative. Clinical therapeutics 30(Suppl B):S50–S51CrossRefPubMed Schellekens H (2008) The immunogenicity of therapeutic proteins and the Fabry antibody standardization initiative. Clinical therapeutics 30(Suppl B):S50–S51CrossRefPubMed
go back to reference Tanaka A, Takeda T, Hoshina T, Fukai K, Yamano T (2010) Enzyme replacement therapy in a patient with Fabry disease and the development of IgE antibodies against agalsidase beta but not agalsidase alpha. J Inherit Metab Dis [Epub ahead of print] Tanaka A, Takeda T, Hoshina T, Fukai K, Yamano T (2010) Enzyme replacement therapy in a patient with Fabry disease and the development of IgE antibodies against agalsidase beta but not agalsidase alpha. J Inherit Metab Dis [Epub ahead of print]
go back to reference Whitfield PD, Calvin J, Hogg S et al (2005) Monitoring enzyme replacement therapy in Fabry disease–role of urine globotriaosylceramide. J nherit Metab Dis 28(1):21–33 Whitfield PD, Calvin J, Hogg S et al (2005) Monitoring enzyme replacement therapy in Fabry disease–role of urine globotriaosylceramide. J nherit Metab Dis 28(1):21–33
Metadata
Title
Letter concerning “Enzyme replacement therapy in a patient with Fabry disease and the development of IgE antibodies against agalsidase beta but not agalsidase alpha”, by Tanaka et al.
Authors
Gabor E. Linthorst
Johannes M. F. G. Aerts
Publication date
01-02-2011
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 1/2011
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-010-9219-y

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