TY - JOUR
T1 - Replacement therapy in Mucopolysaccharidosis type VI
T2 - Advantages of early onset of therapy
AU - Auclair, Dyane
AU - Hopwood, John J.
AU - Brooks, Douglas A.
AU - Lemontt, Jeffrey F.
AU - Crawley, Allison C.
N1 - Funding Information:
The authors gratefully acknowledge the animal care staff at the Institute of Medical and Veterinary Science for the daily care of the cat colony. We also thank Dr. Stuart Swiedler and Ms. Teresa Johnk from BioMarin Pharmaceutical Inc. for their regular support and input, Dr. Stephen Kania from the Department of Comparative Medicine, University of Tennessee, Knoxville, TN regarding complement assays, Ms. Chris Boulter regarding tissue distribution assay and Ms. Margaret McClaren for assistance with histology. BioMarin Pharmaceutical Inc. and the National Health and Medical Research Council of Australia supported this work. The original cats heterogenous for MPS-VI (National Institute of Health DK 25759) given by Prof. Mark Haskins from the University of Pennsylvania is gratefully acknowledged.
PY - 2003/3/1
Y1 - 2003/3/1
N2 - This study evaluates the immunological response following weekly 2h infusions of recombinant human N-acetylgalactosamine 4-sulfatase (rh4S) in Mucopolysaccharidosis VI (MPS VI) cats. The results of three trials (Trial "A": 9 month duration with onset at 3-5 months of age, n=5; and Trials "B" and "C": 6 month duration starting at birth, n=9) were compared. No detrimental effects were noted throughout Trials B and C. Temporary hypersensitivity reactions (e.g., vomiting, diarrhoea) occurred in four cats in Trial A and were alleviated by increasing the dose of antihistamine premedication and the duration of infusion. All cats in Trial A developed antibodies to rh4S (range of final titres: 1041-134,931). All cats treated from birth showed negligible titres (range: <50-598). In vitro inhibition of rh4S activity (up to 47%) was demonstrated with plasma from four cats with elevated titres. Significant reduction of urinary glycosaminoglycan concentration in all cats indicated the ability of rh4S to metabolize stored substrates regardless of the presence of circulating antibodies. Similarly, lysosomal storage in reticuloendothelial cells and fibroblasts of kidney interstistium, dura and skin was reduced in all cats irrespective of their antibody titre although cats with elevated titre had less beneficial effect on cardiovascular tissues (aorta smooth muscle cells, heart valve fibroblasts). Overall improvement in the disease condition (at physical, neurological, and skeletal levels) was most pronounced for cats treated from birth compared with cats treated at a later age.
AB - This study evaluates the immunological response following weekly 2h infusions of recombinant human N-acetylgalactosamine 4-sulfatase (rh4S) in Mucopolysaccharidosis VI (MPS VI) cats. The results of three trials (Trial "A": 9 month duration with onset at 3-5 months of age, n=5; and Trials "B" and "C": 6 month duration starting at birth, n=9) were compared. No detrimental effects were noted throughout Trials B and C. Temporary hypersensitivity reactions (e.g., vomiting, diarrhoea) occurred in four cats in Trial A and were alleviated by increasing the dose of antihistamine premedication and the duration of infusion. All cats in Trial A developed antibodies to rh4S (range of final titres: 1041-134,931). All cats treated from birth showed negligible titres (range: <50-598). In vitro inhibition of rh4S activity (up to 47%) was demonstrated with plasma from four cats with elevated titres. Significant reduction of urinary glycosaminoglycan concentration in all cats indicated the ability of rh4S to metabolize stored substrates regardless of the presence of circulating antibodies. Similarly, lysosomal storage in reticuloendothelial cells and fibroblasts of kidney interstistium, dura and skin was reduced in all cats irrespective of their antibody titre although cats with elevated titre had less beneficial effect on cardiovascular tissues (aorta smooth muscle cells, heart valve fibroblasts). Overall improvement in the disease condition (at physical, neurological, and skeletal levels) was most pronounced for cats treated from birth compared with cats treated at a later age.
KW - Enzyme replacement therapy
KW - Immune response
KW - Lysosomal storage diseases
KW - MPS VI
KW - N-Acetylgalactosamine 4-sulfatase
UR - https://www.scopus.com/pages/publications/0037343066
U2 - 10.1016/S1096-7192(03)00007-6
DO - 10.1016/S1096-7192(03)00007-6
M3 - Article
C2 - 12649061
AN - SCOPUS:0037343066
SN - 1096-7192
VL - 78
SP - 163
EP - 174
JO - Molecular Genetics and Metabolism
JF - Molecular Genetics and Metabolism
IS - 3
ER -