AbstractImmune responses to enzyme replacement therapy (ERT) have been reported and can result in a hypersensitivity/anaphylactic reaction during or immediately after enzyme infusion. We have investigated the infusion of the lysosomal enzyme N-acetylgalactosamine 4-sulphatase (4-sulphatase) into immunized, high titre rats as a model of immune response to ERT. To simulate ERT, high and low titre rats were infused with different doses of radiolabelled recombinant human 4-sulphatase (3H-rh4S). There was evidence of altered targeting, inactivation and degradation of 4-sulphatase in high titre (titre 1 024 000) compared to low titre (titre 64) rats. There was more 4-sulphatase enzyme activity detected in 5 mg/kg high titre rats when compared to ...
The US Food and Drug Administration (FDA) and National Organization for Rare Disease (NORD) convened...
Enzyme replacement therapy (ERT) is the current standard of care for Mucopolysaccharidosis type VI (...
A deficiency of arylsulfatase A (ASA) causes metachromatic leukodystrophy (MLD), a lysosomal storage...
Immune responses to enzyme replacement therapy (ERT) have been reported and can result in a hypersen...
AbstractEnzyme replacement therapy (ERT) can potentially result in an immunological response to the ...
Enzyme replacement therapy (ERT) can potentially result in an immunological response to the introduc...
Enzyme replacement therapy (ERT) has been developed and trialed for the treatment of human lysosomal...
The mucopolysaccharidoses (MPS) are a group of multiple pathology disorders which are part of a larg...
The lysosomal storage disorders (LSD) are a group of severe multiple pathology disorders characteriz...
Lysosomal storage diseases (LSDs) are rare genetic metabolic disorders that cause the accumulation o...
Immune response to replacement therapy has been reported for a range of therapeutic strategies being...
Enzyme replacement therapy (ERT) is a treatment option for several lysosomal disorders including the...
Lysosomal storage disorders are collectively important because they cause significant morbidity and ...
Mucopolysaccharidosis IVA (MPS IVA) is an autosomal recessive disorder caused by a deficiency of N-a...
AbstractEnzyme replacement therapy (ERT) has proven to be an effective therapy for some lysosomal st...
The US Food and Drug Administration (FDA) and National Organization for Rare Disease (NORD) convened...
Enzyme replacement therapy (ERT) is the current standard of care for Mucopolysaccharidosis type VI (...
A deficiency of arylsulfatase A (ASA) causes metachromatic leukodystrophy (MLD), a lysosomal storage...
Immune responses to enzyme replacement therapy (ERT) have been reported and can result in a hypersen...
AbstractEnzyme replacement therapy (ERT) can potentially result in an immunological response to the ...
Enzyme replacement therapy (ERT) can potentially result in an immunological response to the introduc...
Enzyme replacement therapy (ERT) has been developed and trialed for the treatment of human lysosomal...
The mucopolysaccharidoses (MPS) are a group of multiple pathology disorders which are part of a larg...
The lysosomal storage disorders (LSD) are a group of severe multiple pathology disorders characteriz...
Lysosomal storage diseases (LSDs) are rare genetic metabolic disorders that cause the accumulation o...
Immune response to replacement therapy has been reported for a range of therapeutic strategies being...
Enzyme replacement therapy (ERT) is a treatment option for several lysosomal disorders including the...
Lysosomal storage disorders are collectively important because they cause significant morbidity and ...
Mucopolysaccharidosis IVA (MPS IVA) is an autosomal recessive disorder caused by a deficiency of N-a...
AbstractEnzyme replacement therapy (ERT) has proven to be an effective therapy for some lysosomal st...
The US Food and Drug Administration (FDA) and National Organization for Rare Disease (NORD) convened...
Enzyme replacement therapy (ERT) is the current standard of care for Mucopolysaccharidosis type VI (...
A deficiency of arylsulfatase A (ASA) causes metachromatic leukodystrophy (MLD), a lysosomal storage...