Toward reducing immunogenicity of enzyme replacement therapy: altering the specificity of human β-glucuronidase to compensate for α-iduronidase deficiency-Reference-Cited by-同舟云学术

Toward reducing immunogenicity of enzyme replacement therapy: altering the specificity of human β-glucuronidase to compensate for α-iduronidase deficiency

Published:2015-08-28 Issue:11 Volume:28 Page:519-530
ISSN:1741-0126
Container-title:Protein Engineering Design and Selection
language:en
Short-container-title:Protein Engineering, Design and Selection

Author:

Chuang Huai-Yao,Suen Ching-Shu,Hwang Ming-Jing,Roffler Steve R.

Funder

Ministry of Science and Technology, Taipei, Taiwan

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Biochemistry,Bioengineering,Biotechnology

Link

http://academic.oup.com/peds/article-pdf/28/11/519/17494969/gzv041.pdf

Reference55 articles.

1. Persistence of high sustained antibodies to enzyme replacement therapy despite extensive immunomodulatory therapy in an infant with Pompe disease: Need for agents to target antibody-secreting plasma cells

2. Algorithm for the Early Diagnosis and Treatment of Patients with Cross Reactive Immunologic Material-Negative Classic Infantile Pompe Disease: A Step towards Improving the Efficacy of ERT

3. Therapeutic enzyme deimmunization by combinatorial T-cell epitope removal using neutral drift

4. Signal for Attachment of a Phospholipid Membrane Anchor in Decay Accelerating Factor

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