Long-term intra-articular administration of recombinant human N-acetylgalactosamine-4-sulfatase in feline mucopolysaccharidosis VI

被引:24
作者
Auclair, Dyane
Hopwood, John J.
Lemontt, Jeffrey F.
Chen, Lin
Byers, Sharon
机构
[1] Children Youth & Womens Hlth Serv, Dept Med Genet, Matrix Biol Unit, Adelaide, SA 5006, Australia
[2] Children Youth & Womens Hlth Serv, Dept Med Genet, Lysosomal Dis Res Unit, Adelaide, SA 5006, Australia
[3] BioMarin Pharmaceut Inc, Novato, CA 94949 USA
[4] Univ Adelaide, Dept Paediat, Adelaide, SA 5005, Australia
基金
英国医学研究理事会;
关键词
joint disease; intra-articular injection; enzyme replacement therapy; mucopolysacchariclosis type VI cartilage; synovium;
D O I
10.1016/j.ymgme.2007.04.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Degenerative joint disease (DJD) is one aspect of mucopolysaccharidosis VI (MPS VI) pathology that has proven resistant to systemic enzyme replacement therapy (ERT). In this study the effect of repeated intra-articular injections (IA INJ) of recombinant human acetylgalactosamine-4-sulfatase (rh4S) on DJD was examined. Four NIPS VI cats received i.v. ERT weekly from birth plus IA INJ (0 or 500 mu g of rh4S per joint; monthly or every three months) while three NIPS VI cats received IA INJ only. After 10 months, shoulders, elbows and knees were compared. Taken individually, an improvement in joint appearance was observed between the joints that received rh4S monthly or every three months compared with the contralateral joints treated with buffer or at lower frequency. Within articular cartilage of joints treated more frequently, the depth of clearance of lysosomal storage tended to be greater and uronic acid content was reduced reflecting the removal of glycosaminoglycans. Synovium in treated joints also showed less storage. No abnormal clinical signs were observed after the IA INJ and negligible antibody titres were measured throughout the study. No clear benefit was observed by combining IA INJ with weekly ERT and the most significant improvement in joint appearance resulted from increased IA INJ frequency. These data support the view that intra-articular therapy may be a good option for preventing the development of the severe articular pathology in MPS VI. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:352 / 361
页数:10
相关论文
共 31 条
[1]   Intra-articular enzyme administration for joint disease in feline mucopolysaccharidosis VI: Enzyme dose and interval [J].
Auclair, D ;
Hein, LK ;
Hopwood, JJ ;
Byers, S .
PEDIATRIC RESEARCH, 2006, 59 (04) :538-543
[2]   Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapy [J].
Auclair, D ;
Hopwood, JJ ;
Brooks, DA ;
Lemontt, JF ;
Crawley, AC .
MOLECULAR GENETICS AND METABOLISM, 2003, 78 (03) :163-174
[3]   NEW METHOD FOR QUANTITATIVE-DETERMINATION OF URONIC ACIDS [J].
BLUMENKR.N ;
ASBOEHAN.G .
ANALYTICAL BIOCHEMISTRY, 1973, 54 (02) :484-489
[4]  
BRETON L, 1983, J AM ANIM HOSP ASSOC, V19, P891
[5]   Effect of enzyme replacement therapy on bone formation in a feline model of mucopolysaccharidosis type VI [J].
Byers, S ;
Nuttall, JD ;
Crawley, AC ;
Hopwood, JJ ;
Smith, K ;
Fazzalari, NL .
BONE, 1997, 21 (05) :425-431
[6]   Enzyme replacement therapy in a feline model of MPS VI: Modification of enzyme structure and dose frequency [J].
Byers, S ;
Crawley, AC ;
Brumfield, LK ;
Nuttall, JD ;
Hopwood, JJ .
PEDIATRIC RESEARCH, 2000, 47 (06) :743-749
[7]  
COWELL KR, 1976, J AM VET MED ASSOC, V169, P334
[8]   Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypes [J].
Crawley, AC ;
Yogalingam, G ;
Muller, VJ ;
Hopwood, JJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (01) :109-119
[9]   Enzyme replacement therapy from birth in a feline model of mucopolysaccharidosis type VI [J].
Crawley, AC ;
Niedzielski, KH ;
Isaac, EL ;
Davey, RCA ;
Byers, S ;
Hopwood, JJ .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (04) :651-662
[10]   Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome [J].
Crawley, AC ;
Brooks, DA ;
Muller, VJ ;
Petersen, BA ;
Isaac, EL ;
Bielicki, J ;
King, BM ;
Boulter, CD ;
Moore, AJ ;
Fazzalari, NL ;
Anson, DS ;
Byers, S ;
Hopwood, JJ .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (08) :1864-1873