| Literature DB >> 25842186 |
Phillip A Doerfler1, Sushrusha Nayak2, Roland W Herzog3, Laurence Morel4, Barry J Byrne5.
Abstract
Antibodies formed against the therapeutic protein are a life-threatening complication that arises during enzyme replacement therapy for Pompe disease (acid α-glucosidase deficiency; GAA). To provide an effective alternative to current practices, we investigated the capacity of anti-B-cell activating factor (BAFF) as a novel drug candidate to prevent antibody formation in a Pompe disease mouse model. A BAFF-neutralizing antibody was administered prophylactically and with maintenance doses in association with enzyme replacement therapy using recombinant human GAA in Gaa(-/-) mice. BAFF blockade delayed antibody production and increased GAA activity within tissues with protection from anaphylaxis. Anti-BAFF also resolved antibody formation during an immune response and precluded the maturation of antibody secreting cells from entering the bone marrow compartment. This treatment modality may therefore be a viable alternative for the clinical management of antibody formation for Pompe disease and has potential use against antibody formation in other protein replacement therapies.Entities:
Keywords: Acid alpha-glucosidase; BAFF; BLyS; Enzyme replacement therapy; Pompe disease
Mesh:
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Year: 2015 PMID: 25842186 PMCID: PMC4464966 DOI: 10.1016/j.clim.2015.03.022
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969