| Literature DB >> 23620524 |
Federica Deodato1, Virginia Maria Ginocchio2, Alfredo Onofri3, Giorgia Grutter4, Alessandro Germani3, Carlo Dionisi-Vici2.
Abstract
Infantile Pompe disease, resulting from deficiency of lysosomal acid α-glucosidase, requires enzyme replacement therapy with recombinant human acid α-glucosidase. Most patients develop antirecombinant human acid α-glucosidase antibodies, leading to reduced response to enzyme therapy in a subgroup of them. Aiming to improve treatment response, several immune tolerance induction strategies have been explored. We describe a patient with life-threatening infusion-associated reactions presenting anti-recombinant human acid α-glucosidase antibodies. He was successfully treated with an immune tolerance induction protocol, consisting of plasma exchange combined with a single dose of rituximab. Immediate reduction of antibody titer was obtained and enzyme therapy was resumed without infusion-associated reactions. Twenty-two months later, immunoglobulin G titer remained below 1:100. In conclusion, we applied a short-course immune tolerance induction strategy in a patient with severe infusion-associated reactions and anti-recombinant human acid α-glucosidase antibodies, leading to early and persisting reduction of antibody titer, in the absence of significant adverse events.Entities:
Keywords: Pompe; anti-recombinant human acid α-glucosidase antibodies; immune modulation; lysosomal; rituximab
Mesh:
Substances:
Year: 2013 PMID: 23620524 DOI: 10.1177/0883073813485819
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987