The Interaction of Innate and Adaptive Immunity and Stabilization of Mast Cell Activation in Management of Infusion Related Reactions in Patients with Fabry Disease

Fabry disease (FD) is an X-linked lysosomal disorder caused by mutations in <i>GLA</i> gene resulting in lack of or faulty α-galactosidase A (α-GalA) enzyme. Enzyme replacement therapy (ERT) with recombinant human α-GalA enzyme (agalsidase) is the standard treatment option for FD. Infusi...

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Bibliographic Details
Main Authors: Renuka P. Limgala, Jaqueline Fikry, Vasudha Veligatla, Ozlem Goker-Alpan
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/19/7213