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Erschienen in: Drugs 18/2007

01.12.2007 | Review Article

Treatment of Lysosomal Storage Disorders

Progress with Enzyme Replacement Therapy

verfasst von: Marianne Rohrbach, Dr Joe T. R. Clarke

Erschienen in: Drugs | Ausgabe 18/2007

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Abstract

Enzyme replacement therapy (ERT) as treatment for lysosomal storage diseases (LSDs) was suggested as long ago as 1966 by De Duve and Wattiaux. However, it took >35 years to demonstrate the safety and effectiveness of ERT for type 1 Gaucher’s disease. An important breakthrough was certainly the enactment of legislation in the US, designed to encourage commercialisation of products developed in academic institutions for pharmaceutical companies to invest in treatments for rare diseases. The principles elaborated in the development of the treatment of Gaucher’s disease were subsequently applied to the development of ERT of other LSDs. The safety and effectiveness of ERT for Fabry’s disease, mucopolysaccharidoses (MPS) I, MPS II and MPS VI, as well as for Pompe’s disease have been demonstrated in well designed clinical trials, and the treatments are now commercially available throughout the world. Several questions remain to be answered. The long-term effectiveness of most of the treatments has not yet been established. What is reversible by ERT and what may not be reversible but is preventable, is not yet clear. The pathology in some tissues, such as the brain, is inaccessible to ERT, indicating that some manifestations of the LSD will not respond to the treatment. The extent of this problem is still unclear. The cost of ERT is very high, creating problems for third-party payers, which has strained reimbursement schemes based on the demonstration of acceptable cost effectiveness. ERT of LSDs represents the most important advance in the treatment of this class of diseases. The information that is currently being collected as part of large-scale observational studies will help to establish the full potential of the treatment.
Literatur
1.
Zurück zum Zitat Futerman AH, van Meer G. The cell biology of lysosomal storage disorders. Nat Rev Mol Cell Biol 2004 Jul; 5(7): 554–65PubMedCrossRef Futerman AH, van Meer G. The cell biology of lysosomal storage disorders. Nat Rev Mol Cell Biol 2004 Jul; 5(7): 554–65PubMedCrossRef
2.
Zurück zum Zitat Elleder M. Glucosylceramide transfer from lysosomes: the missing link in molecular pathology of glucosylceramidase deficiency: a hypothesis based on existing data. J Inherit Metab Dis 2006 Dec; 29(6): 707–15PubMedCrossRef Elleder M. Glucosylceramide transfer from lysosomes: the missing link in molecular pathology of glucosylceramidase deficiency: a hypothesis based on existing data. J Inherit Metab Dis 2006 Dec; 29(6): 707–15PubMedCrossRef
4.
Zurück zum Zitat Bright NA, Reaves BJ, Mullock BM, et al. Dense core lysosomes can fuse with late endosomes and are re-formed from the resultant hybrid organelles. J Cell Sci 1997 Sep; 110 (Pt 17): 2027–40PubMed Bright NA, Reaves BJ, Mullock BM, et al. Dense core lysosomes can fuse with late endosomes and are re-formed from the resultant hybrid organelles. J Cell Sci 1997 Sep; 110 (Pt 17): 2027–40PubMed
5.
Zurück zum Zitat Stinchcombe JC, Page LJ, Griffiths GM. Secretory lysosome biogenesis in cytotoxic T lymphocytes from normal and Chediak Higashi syndrome patients. Traffic 2000 May; 1(5): 435–44PubMedCrossRef Stinchcombe JC, Page LJ, Griffiths GM. Secretory lysosome biogenesis in cytotoxic T lymphocytes from normal and Chediak Higashi syndrome patients. Traffic 2000 May; 1(5): 435–44PubMedCrossRef
6.
Zurück zum Zitat Gu F, Gruenberg J. Biogenesis of transport intermediates in the endocytic pathway. FEBS Lett 1999 Jun 4; 452 (1-2): 61–6PubMedCrossRef Gu F, Gruenberg J. Biogenesis of transport intermediates in the endocytic pathway. FEBS Lett 1999 Jun 4; 452 (1-2): 61–6PubMedCrossRef
7.
Zurück zum Zitat Sabatini DD, Adesnik MB. The biogenesis of membranes and organelles. In: Scriver CR, Beaudet AL, Sly WS, et al., editors. The metabolic and molecular bases of inherited disease. 8th ed. New York: McGraw-Hill, 2001: 433–517 Sabatini DD, Adesnik MB. The biogenesis of membranes and organelles. In: Scriver CR, Beaudet AL, Sly WS, et al., editors. The metabolic and molecular bases of inherited disease. 8th ed. New York: McGraw-Hill, 2001: 433–517
8.
Zurück zum Zitat Kornfeld S. Lysosomal enzyme targeting. Biochem Soc Trans 1990 Jun; 18(3): 367–74PubMed Kornfeld S. Lysosomal enzyme targeting. Biochem Soc Trans 1990 Jun; 18(3): 367–74PubMed
9.
Zurück zum Zitat Ghosh P, Dahms NM, Kornfeld S. Mannose 6-phosphate receptors: new twists in the tale. Nat Rev Mol Cell Biol 2003 Mar; 4(3): 202–12PubMedCrossRef Ghosh P, Dahms NM, Kornfeld S. Mannose 6-phosphate receptors: new twists in the tale. Nat Rev Mol Cell Biol 2003 Mar; 4(3): 202–12PubMedCrossRef
10.
Zurück zum Zitat Reitman ML, Lang L, Kornfeld S. UDP-N-acetylglucosamine: lysosomal enzyme N-acetylglucosamine-1-phosphotransferase. Methods Enzymol 1984; 107: 163–72PubMedCrossRef Reitman ML, Lang L, Kornfeld S. UDP-N-acetylglucosamine: lysosomal enzyme N-acetylglucosamine-1-phosphotransferase. Methods Enzymol 1984; 107: 163–72PubMedCrossRef
11.
Zurück zum Zitat Waheed A, Hasilik A, von Figura K. Processing of the phosphorylated recognition marker in lysosomal enzymes: characterization and partial purification of a microsomal alpha-N-acetylglucosaminyl phosphodiesterase. J Biol Chem 1981 Jun 10; 256(11): 5717–21PubMed Waheed A, Hasilik A, von Figura K. Processing of the phosphorylated recognition marker in lysosomal enzymes: characterization and partial purification of a microsomal alpha-N-acetylglucosaminyl phosphodiesterase. J Biol Chem 1981 Jun 10; 256(11): 5717–21PubMed
12.
Zurück zum Zitat Neufeld EF, Muenzer J. The mucopolysaccharidoses. In: Scriver CR, Beaudet AL, Sly WS, et al., editors. The metabolic and molecular bases of inherited disease. 8th ed. New York: McGraw-Hill, 2001: 3421–52 Neufeld EF, Muenzer J. The mucopolysaccharidoses. In: Scriver CR, Beaudet AL, Sly WS, et al., editors. The metabolic and molecular bases of inherited disease. 8th ed. New York: McGraw-Hill, 2001: 3421–52
13.
Zurück zum Zitat Desnick RJ. Enzyme therapy in genetic diseases: II. New York: Alan R. Liss, 1980 Desnick RJ. Enzyme therapy in genetic diseases: II. New York: Alan R. Liss, 1980
14.
Zurück zum Zitat Desnick RJ, Bernlohr RW, Krivit W. Enzyme therapy in genetic diseases, birth defects. New York: The National Foundation, 1973 Desnick RJ, Bernlohr RW, Krivit W. Enzyme therapy in genetic diseases, birth defects. New York: The National Foundation, 1973
15.
Zurück zum Zitat Brady RO, Murray GJ, Barton NW. Modifying exogenous glucocerebrosidase for effective replacement therapy in Gaucher disease. J Inherit Metab Dis 1994; 17(4): 510–9PubMedCrossRef Brady RO, Murray GJ, Barton NW. Modifying exogenous glucocerebrosidase for effective replacement therapy in Gaucher disease. J Inherit Metab Dis 1994; 17(4): 510–9PubMedCrossRef
16.
Zurück zum Zitat Brady RO, Kanfer JN, Shapiro D. Metabolism of glucocerebrosides. II. Evidence of an enzymatic deficiency in Gaucher’s disease. Biochem Biophys Res Commun 1965 Jan 18; 18: 221–5 Brady RO, Kanfer JN, Shapiro D. Metabolism of glucocerebrosides. II. Evidence of an enzymatic deficiency in Gaucher’s disease. Biochem Biophys Res Commun 1965 Jan 18; 18: 221–5
17.
Zurück zum Zitat Di Rocco M, Allegri AE, Grossi S, et al. Gaucher disease phenotype. J Pediatr 2004 Dec; 145(6): 860PubMed Di Rocco M, Allegri AE, Grossi S, et al. Gaucher disease phenotype. J Pediatr 2004 Dec; 145(6): 860PubMed
18.
Zurück zum Zitat Zimran A, Gelbart T, Westwood B, et al. High frequency of the Gaucher disease mutation at nucleotide 1226 among Ashkenazi Jews. Am J Hum Genet 1991; 49: 855–9PubMed Zimran A, Gelbart T, Westwood B, et al. High frequency of the Gaucher disease mutation at nucleotide 1226 among Ashkenazi Jews. Am J Hum Genet 1991; 49: 855–9PubMed
19.
Zurück zum Zitat Brady RO, Kanfer JN, Bradley RM, et al. Demonstration of a deficiency of glucocerebroside-cleaving enzyme in Gaucher’s disease. J Clin Invest 1966 Jul; 45(7): 1112–5PubMedCrossRef Brady RO, Kanfer JN, Bradley RM, et al. Demonstration of a deficiency of glucocerebroside-cleaving enzyme in Gaucher’s disease. J Clin Invest 1966 Jul; 45(7): 1112–5PubMedCrossRef
20.
Zurück zum Zitat Brady RO, Tallman JF, Johnson WG, et al. Replacement therapy for inherited enzyme deficiency: use of purified ceramide-trihexosidase in Fabry’s disease. N Engl J Med 1973 Jul 5; 289(1): 9–14PubMedCrossRef Brady RO, Tallman JF, Johnson WG, et al. Replacement therapy for inherited enzyme deficiency: use of purified ceramide-trihexosidase in Fabry’s disease. N Engl J Med 1973 Jul 5; 289(1): 9–14PubMedCrossRef
21.
Zurück zum Zitat Barton NW, Brady RO, Dambrosia JM, et al. Replacement therapy for inherited enzyme deficiency: macrophage-targeted glucocerebrosidase for Gaucher’s disease. N Engl J Med 1991 May 23; 324(21): 1464–70PubMedCrossRef Barton NW, Brady RO, Dambrosia JM, et al. Replacement therapy for inherited enzyme deficiency: macrophage-targeted glucocerebrosidase for Gaucher’s disease. N Engl J Med 1991 May 23; 324(21): 1464–70PubMedCrossRef
22.
Zurück zum Zitat Grabowski GA, Barton NW, Pastores G, et al. Enzyme therapy in type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources. Ann Intern Med 1995 Jan 1; 122(1): 33–9PubMed Grabowski GA, Barton NW, Pastores G, et al. Enzyme therapy in type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources. Ann Intern Med 1995 Jan 1; 122(1): 33–9PubMed
23.
Zurück zum Zitat Weinreb NJ, Charrow J, Andersson HC, et al. Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry. Am J Med 2002 Aug 1; 113(2): 112–9PubMedCrossRef Weinreb NJ, Charrow J, Andersson HC, et al. Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry. Am J Med 2002 Aug 1; 113(2): 112–9PubMedCrossRef
24.
Zurück zum Zitat Grabowski GA. Gaucher disease: lessons from a decade of therapy. J Pediatr 2004 May; 144 (5 Suppl.): S15–9PubMedCrossRef Grabowski GA. Gaucher disease: lessons from a decade of therapy. J Pediatr 2004 May; 144 (5 Suppl.): S15–9PubMedCrossRef
25.
Zurück zum Zitat Kaplan P, Mazur A, Manor O, et al. Acceleration of retarded growth in children with Gaucher disease after treatment with alglucerase. J Pediatr 1996 Jul; 129(1): 149–53PubMedCrossRef Kaplan P, Mazur A, Manor O, et al. Acceleration of retarded growth in children with Gaucher disease after treatment with alglucerase. J Pediatr 1996 Jul; 129(1): 149–53PubMedCrossRef
26.
Zurück zum Zitat Kauli R, Zaizov R, Lazar L, et al. Delayed growth and puberty in patients with Gaucher disease type 1: natural history and effect of splenectomy and/or enzyme replacement therapy. Isr Med Assoc J 2000 Feb; 2(2): 158–63PubMed Kauli R, Zaizov R, Lazar L, et al. Delayed growth and puberty in patients with Gaucher disease type 1: natural history and effect of splenectomy and/or enzyme replacement therapy. Isr Med Assoc J 2000 Feb; 2(2): 158–63PubMed
27.
Zurück zum Zitat Starzyk K, Richards S, Yee J, et al. The long-term international safety experience of imiglucerase therapy for Gaucher disease. Mol Genet Metab 2007 Feb; 90(2): 157–63PubMedCrossRef Starzyk K, Richards S, Yee J, et al. The long-term international safety experience of imiglucerase therapy for Gaucher disease. Mol Genet Metab 2007 Feb; 90(2): 157–63PubMedCrossRef
28.
Zurück zum Zitat Beutler E. Lysosomal storage diseases: natural history and ethical and economic aspects. Mol Genet Metab 2006 Jul; 88(3): 208–15PubMedCrossRef Beutler E. Lysosomal storage diseases: natural history and ethical and economic aspects. Mol Genet Metab 2006 Jul; 88(3): 208–15PubMedCrossRef
29.
Zurück zum Zitat Clarke JT. Is the current approach to reviewing new drugs condemning the victims of rare diseases to death? A call for a national orphan drug review policy. CMAJ 2006 Jan 17; 174(2): 189–90PubMedCrossRef Clarke JT. Is the current approach to reviewing new drugs condemning the victims of rare diseases to death? A call for a national orphan drug review policy. CMAJ 2006 Jan 17; 174(2): 189–90PubMedCrossRef
30.
Zurück zum Zitat Schiffmann R, Heyes MP, Aerts JM, et al. Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher’s disease. Ann Neurol 1997 Oct; 42(4): 613–21PubMedCrossRef Schiffmann R, Heyes MP, Aerts JM, et al. Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher’s disease. Ann Neurol 1997 Oct; 42(4): 613–21PubMedCrossRef
31.
Zurück zum Zitat Altarescu G, Hill S, Wiggs E, et al. The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher’s disease. J Pediatr 2001 Apr; 138(4): 539–47PubMedCrossRef Altarescu G, Hill S, Wiggs E, et al. The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher’s disease. J Pediatr 2001 Apr; 138(4): 539–47PubMedCrossRef
32.
Zurück zum Zitat Cox T, Lachmann R, Hollak C, et al. Novel oral treatment of Gaucher’s disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis. Lancet 2000 Apr 29; 355(9214): 1481–5PubMedCrossRef Cox T, Lachmann R, Hollak C, et al. Novel oral treatment of Gaucher’s disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis. Lancet 2000 Apr 29; 355(9214): 1481–5PubMedCrossRef
33.
Zurück zum Zitat Prows CA, Sanchez N, Daugherty C, et al. Gaucher disease: enzyme therapy in the acute neuronopathic variant. Am J Med Genet 1997 Jul 11; 71(1): 16–21PubMedCrossRef Prows CA, Sanchez N, Daugherty C, et al. Gaucher disease: enzyme therapy in the acute neuronopathic variant. Am J Med Genet 1997 Jul 11; 71(1): 16–21PubMedCrossRef
34.
Zurück zum Zitat Zimran A, Hollak CE, Abrahamov A, et al. Home treatment with intravenous enzyme replacement therapy for Gaucher disease: an international collaborative study of 33 patients. Blood 1993 Aug 15; 82(4): 1107–9PubMed Zimran A, Hollak CE, Abrahamov A, et al. Home treatment with intravenous enzyme replacement therapy for Gaucher disease: an international collaborative study of 33 patients. Blood 1993 Aug 15; 82(4): 1107–9PubMed
35.
Zurück zum Zitat Cox TM, Aerts JM, Andria G, et al. The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: a position statement. J Inherit Metab Dis 2003; 26(6): 513–26PubMedCrossRef Cox TM, Aerts JM, Andria G, et al. The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: a position statement. J Inherit Metab Dis 2003; 26(6): 513–26PubMedCrossRef
36.
Zurück zum Zitat Weinreb NJ, Barranger JA, Charrow J, et al. Guidance on the use of miglustat for treating patients with type 1 Gaucher disease. Am J Hematol 2005 Nov; 80(3): 223–9PubMedCrossRef Weinreb NJ, Barranger JA, Charrow J, et al. Guidance on the use of miglustat for treating patients with type 1 Gaucher disease. Am J Hematol 2005 Nov; 80(3): 223–9PubMedCrossRef
37.
Zurück zum Zitat Branton M, Schiffmann R, Kopp JB. Natural history and treatment of renal involvement in Fabry disease. J Am Soc Nephrol 2002 Jun; 13 Suppl. 2: S139–43PubMed Branton M, Schiffmann R, Kopp JB. Natural history and treatment of renal involvement in Fabry disease. J Am Soc Nephrol 2002 Jun; 13 Suppl. 2: S139–43PubMed
38.
Zurück zum Zitat Kampmann C, Baehner F, Ries M, et al. Cardiac involvement in Anderson-Fabry disease. J Am Soc Nephrol 2002 Jun; 13 Suppl. 2: S147–9PubMed Kampmann C, Baehner F, Ries M, et al. Cardiac involvement in Anderson-Fabry disease. J Am Soc Nephrol 2002 Jun; 13 Suppl. 2: S147–9PubMed
39.
Zurück zum Zitat Goldman ME, Cantor R, Schwartz MF, et al. Echocardiographic abnormalities and disease severity in Fabry’s disease. J Am Coll Cardiol 1986 May; 7(5): 1157–61PubMedCrossRef Goldman ME, Cantor R, Schwartz MF, et al. Echocardiographic abnormalities and disease severity in Fabry’s disease. J Am Coll Cardiol 1986 May; 7(5): 1157–61PubMedCrossRef
40.
Zurück zum Zitat Linhart A, Palecek T, Bultas J, et al. New insights in cardiac structural changes in patients with Fabry’s disease. Am Heart J 2000 Jun; 139(6): 1101–8PubMedCrossRef Linhart A, Palecek T, Bultas J, et al. New insights in cardiac structural changes in patients with Fabry’s disease. Am Heart J 2000 Jun; 139(6): 1101–8PubMedCrossRef
41.
Zurück zum Zitat Mitsias P, Levine SR. Cerebrovascular complications of Fabry’s disease. Ann Neurol 1996 Jul; 40(1): 8–17PubMedCrossRef Mitsias P, Levine SR. Cerebrovascular complications of Fabry’s disease. Ann Neurol 1996 Jul; 40(1): 8–17PubMedCrossRef
42.
Zurück zum Zitat Mendez MF, Stanley TM, Medel NM, et al. The vascular dementia of Fabry’s disease. Dement Geriatr Cogn Disord 1997 Jul–Aug; 8(4): 252–7PubMedCrossRef Mendez MF, Stanley TM, Medel NM, et al. The vascular dementia of Fabry’s disease. Dement Geriatr Cogn Disord 1997 Jul–Aug; 8(4): 252–7PubMedCrossRef
43.
Zurück zum Zitat Schiffmann R, Kopp JB, Austin HA, et al. Enzyme replacement therapy in Fabry disease: a randomized controlled trial. JAMA 2001 Jun 6; 285(21): 2743–9PubMedCrossRef Schiffmann R, Kopp JB, Austin HA, et al. Enzyme replacement therapy in Fabry disease: a randomized controlled trial. JAMA 2001 Jun 6; 285(21): 2743–9PubMedCrossRef
44.
Zurück zum Zitat Sirrs SM, Clarke JTR. Agalsidase alpha therapy for Fabry disease. Expert Rev Endocrinol Metab 2007; 2(2): 147–54CrossRef Sirrs SM, Clarke JTR. Agalsidase alpha therapy for Fabry disease. Expert Rev Endocrinol Metab 2007; 2(2): 147–54CrossRef
45.
Zurück zum Zitat Eng CM, Banikazemi M, Gordon RE, et al. A phase 1/2 clinical trial of enzyme replacement in fabry disease: pharmacokinetic, substrate clearance, and safety studies. Am J Hum Genet 2001 Mar; 68(3): 711–22PubMedCrossRef Eng CM, Banikazemi M, Gordon RE, et al. A phase 1/2 clinical trial of enzyme replacement in fabry disease: pharmacokinetic, substrate clearance, and safety studies. Am J Hum Genet 2001 Mar; 68(3): 711–22PubMedCrossRef
46.
Zurück zum Zitat Eng CM, Guffon N, Wilcox WR, et al. Safety and efficacy of recombinant human alpha-galactosidase A: replacement therapy in Fabry’s disease. N Engl J Med 2001 Jul 5; 345(1): 9–16PubMedCrossRef Eng CM, Guffon N, Wilcox WR, et al. Safety and efficacy of recombinant human alpha-galactosidase A: replacement therapy in Fabry’s disease. N Engl J Med 2001 Jul 5; 345(1): 9–16PubMedCrossRef
47.
Zurück zum Zitat Thurberg BL, Randolph Byers H, Granter SR, et al. Monitoring the 3-year efficacy of enzyme replacement therapy in fabry disease by repeated skin biopsies. J Invest Dermatol 2004 Apr; 122(4): 900–8PubMedCrossRef Thurberg BL, Randolph Byers H, Granter SR, et al. Monitoring the 3-year efficacy of enzyme replacement therapy in fabry disease by repeated skin biopsies. J Invest Dermatol 2004 Apr; 122(4): 900–8PubMedCrossRef
48.
Zurück zum Zitat Wilcox WR, Banikazemi M, Guffon N, et al. Long-term safety and efficacy of enzyme replacement therapy for Fabry disease. Am J Hum Genet 2004 Jul; 75(1): 65–74PubMedCrossRef Wilcox WR, Banikazemi M, Guffon N, et al. Long-term safety and efficacy of enzyme replacement therapy for Fabry disease. Am J Hum Genet 2004 Jul; 75(1): 65–74PubMedCrossRef
49.
Zurück zum Zitat Banikazemi M, Bultas J, Waldek S, et al. Agalsidase-beta therapy for advanced Fabry disease: a randomized trial. Ann Intern Med 2007 Jan 16; 146(2): 77–86PubMed Banikazemi M, Bultas J, Waldek S, et al. Agalsidase-beta therapy for advanced Fabry disease: a randomized trial. Ann Intern Med 2007 Jan 16; 146(2): 77–86PubMed
50.
Zurück zum Zitat Thurberg BL, Rennke H, Colvin RB, et al. Globotriaosylceramide accumulation in the Fabry kidney is cleared from multiple cell types after enzyme replacement therapy. Kidney Int 2002 Dec; 62(6): 1933–46PubMedCrossRef Thurberg BL, Rennke H, Colvin RB, et al. Globotriaosylceramide accumulation in the Fabry kidney is cleared from multiple cell types after enzyme replacement therapy. Kidney Int 2002 Dec; 62(6): 1933–46PubMedCrossRef
51.
Zurück zum Zitat Gupta S, Ries M, Kotsopoulos S, et al. The relationship of vascular glycolipid storage to clinical manifestations of Fabry disease: a cross-sectional study of a large cohort of clinically affected heterozygous women. Medicine (Baltimore) 2005 Sep; 84(5): 261–8CrossRef Gupta S, Ries M, Kotsopoulos S, et al. The relationship of vascular glycolipid storage to clinical manifestations of Fabry disease: a cross-sectional study of a large cohort of clinically affected heterozygous women. Medicine (Baltimore) 2005 Sep; 84(5): 261–8CrossRef
52.
Zurück zum Zitat Vedder AC, Linthorst GE, van Breemen MJ, et al. The Dutch Fabry cohort: diversity of clinical manifestations and Gb3 levels. J Inherit Metab Dis 2007 Feb; 30(1): 68–78PubMedCrossRef Vedder AC, Linthorst GE, van Breemen MJ, et al. The Dutch Fabry cohort: diversity of clinical manifestations and Gb3 levels. J Inherit Metab Dis 2007 Feb; 30(1): 68–78PubMedCrossRef
53.
Zurück zum Zitat Clarke JT. Narrative review: Fabry disease. Ann Intern Med 2007 Mar 20; 146(6): 425–33PubMed Clarke JT. Narrative review: Fabry disease. Ann Intern Med 2007 Mar 20; 146(6): 425–33PubMed
54.
Zurück zum Zitat Linthorst GE, Hollak CE, Donker-Koopman WE, et al. Enzyme therapy for Fabry disease: neutralizing antibodies toward agalsidase alpha and beta. Kidney Int 2004 Oct; 66(4): 1589–95PubMedCrossRef Linthorst GE, Hollak CE, Donker-Koopman WE, et al. Enzyme therapy for Fabry disease: neutralizing antibodies toward agalsidase alpha and beta. Kidney Int 2004 Oct; 66(4): 1589–95PubMedCrossRef
55.
Zurück zum Zitat Elleder M, Poupetova H, Kozich V. Fetal pathology in Fabry’s disease and mucopolysaccharidosis type I [in Czech]. Cesk Patol 1998 Jan; 34(1): 7–12PubMed Elleder M, Poupetova H, Kozich V. Fetal pathology in Fabry’s disease and mucopolysaccharidosis type I [in Czech]. Cesk Patol 1998 Jan; 34(1): 7–12PubMed
56.
Zurück zum Zitat Desnick RJ, Brady R, Barranger J, et al. Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy. Ann Intern Med 2003 Feb 18; 138(4): 338–46PubMed Desnick RJ, Brady R, Barranger J, et al. Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy. Ann Intern Med 2003 Feb 18; 138(4): 338–46PubMed
57.
Zurück zum Zitat Lowry RB, Applegarth DA, Toone JR, et al. An update on the frequency of mucopolysaccharide syndromes in British Columbia. Hum Genet 1990 Aug; 85(3): 389–90PubMedCrossRef Lowry RB, Applegarth DA, Toone JR, et al. An update on the frequency of mucopolysaccharide syndromes in British Columbia. Hum Genet 1990 Aug; 85(3): 389–90PubMedCrossRef
58.
Zurück zum Zitat Meikle PJ, Hopwood JJ, Clague AE, et al. Prevalence of lysosomal storage disorders. JAMA 1999 Jan 20; 281(3): 249–54PubMedCrossRef Meikle PJ, Hopwood JJ, Clague AE, et al. Prevalence of lysosomal storage disorders. JAMA 1999 Jan 20; 281(3): 249–54PubMedCrossRef
59.
Zurück zum Zitat Nelson J. Incidence of the mucopolysaccharidoses in Northern Ireland. Hum Genet 1997 Dec; 101(3): 355–8PubMedCrossRef Nelson J. Incidence of the mucopolysaccharidoses in Northern Ireland. Hum Genet 1997 Dec; 101(3): 355–8PubMedCrossRef
60.
Zurück zum Zitat Poorthuis BJ, Wevers RA, Kleijer WJ, et al. The frequency of lysosomal storage diseases in The Netherlands. Hum Genet 1999 Jul–Aug; 105(1–2): 151–6PubMed Poorthuis BJ, Wevers RA, Kleijer WJ, et al. The frequency of lysosomal storage diseases in The Netherlands. Hum Genet 1999 Jul–Aug; 105(1–2): 151–6PubMed
61.
Zurück zum Zitat Scott HS, Bunge S, Gal A, et al. Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications. Hum Mutat 1995; 6(4): 288–302PubMedCrossRef Scott HS, Bunge S, Gal A, et al. Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications. Hum Mutat 1995; 6(4): 288–302PubMedCrossRef
62.
Zurück zum Zitat Whitley CB, Belani KG, Chang PN, et al. Long-term outcome of Hurler syndrome following bone marrow transplantation. Am J Med Genet 1993 Apr 15; 46(2): 209–18PubMedCrossRef Whitley CB, Belani KG, Chang PN, et al. Long-term outcome of Hurler syndrome following bone marrow transplantation. Am J Med Genet 1993 Apr 15; 46(2): 209–18PubMedCrossRef
63.
Zurück zum Zitat Vellodi A, Young EP, Cooper A, et al. Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres. Arch Dis Child 1997 Feb; 76(2): 92–9PubMedCrossRef Vellodi A, Young EP, Cooper A, et al. Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres. Arch Dis Child 1997 Feb; 76(2): 92–9PubMedCrossRef
64.
Zurück zum Zitat Peters C, Shapiro EG, Anderson J, et al. Hurler syndrome: II. Outcome of HLA-genotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty-four children. The Storage Disease Collaborative Study Group. Blood 1998 Apr 1; 91(7): 2601–8 Peters C, Shapiro EG, Anderson J, et al. Hurler syndrome: II. Outcome of HLA-genotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty-four children. The Storage Disease Collaborative Study Group. Blood 1998 Apr 1; 91(7): 2601–8
65.
Zurück zum Zitat Guffon N, Souillet G, Maire I, et al. Follow-up of nine patients with Hurler syndrome after bone marrow transplantation. J Pediatr 1998 Jul; 133(1): 119–25PubMedCrossRef Guffon N, Souillet G, Maire I, et al. Follow-up of nine patients with Hurler syndrome after bone marrow transplantation. J Pediatr 1998 Jul; 133(1): 119–25PubMedCrossRef
66.
Zurück zum Zitat Kakkis ED, Muenzer J, Tiller GE, et al. Enzyme-replacement therapy in mucopolysaccharidosis I. N Engl J Med 2001 Jan 18; 344(3): 182–8PubMedCrossRef Kakkis ED, Muenzer J, Tiller GE, et al. Enzyme-replacement therapy in mucopolysaccharidosis I. N Engl J Med 2001 Jan 18; 344(3): 182–8PubMedCrossRef
67.
Zurück zum Zitat Wraith JE, Clarke LA, Beck M, et al. Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human alpha-L-iduronidase (laronidase). J Pediatr 2004 May; 144(5): 581–8PubMedCrossRef Wraith JE, Clarke LA, Beck M, et al. Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human alpha-L-iduronidase (laronidase). J Pediatr 2004 May; 144(5): 581–8PubMedCrossRef
68.
Zurück zum Zitat Muenzer J, Wraith JE, Beck M, et al. A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome). Genet Med 2006 Aug; 8(8): 465–73PubMedCrossRef Muenzer J, Wraith JE, Beck M, et al. A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome). Genet Med 2006 Aug; 8(8): 465–73PubMedCrossRef
69.
Zurück zum Zitat Muenzer J, Gucsavas-Calikoglu M, McCandless SE, et al. A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome). Mol Genet Metab 2007 Mar; 90(3): 329–37PubMedCrossRef Muenzer J, Gucsavas-Calikoglu M, McCandless SE, et al. A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome). Mol Genet Metab 2007 Mar; 90(3): 329–37PubMedCrossRef
70.
Zurück zum Zitat Harmatz P, Whitley CB, Waber L, et al. Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). J Pediatr 2004 May; 144(5): 574–80PubMedCrossRef Harmatz P, Whitley CB, Waber L, et al. Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). J Pediatr 2004 May; 144(5): 574–80PubMedCrossRef
71.
Zurück zum Zitat Harmatz P, Giugliani R, Schwartz I, et al. Enzyme replacement therapy for mucopolysaccharidosis VI: a phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, openlabel extension study. J Pediatr 2006 Apr; 148(4): 533–9PubMedCrossRef Harmatz P, Giugliani R, Schwartz I, et al. Enzyme replacement therapy for mucopolysaccharidosis VI: a phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, openlabel extension study. J Pediatr 2006 Apr; 148(4): 533–9PubMedCrossRef
72.
Zurück zum Zitat Krivit W, Pierpont ME, Ayaz K, et al. Bone-marrow transplantation in the Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI): biochemical and clinical status 24 months after transplantation. N Engl J Med 1984 Dec 20; 311(25): 1606–11PubMedCrossRef Krivit W, Pierpont ME, Ayaz K, et al. Bone-marrow transplantation in the Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI): biochemical and clinical status 24 months after transplantation. N Engl J Med 1984 Dec 20; 311(25): 1606–11PubMedCrossRef
73.
Zurück zum Zitat Hirschhorn R, Reuser AJJ. Glycogen storage disease type II: acid alpha-glucosidase (acid maltase) deficiency. In: Scriver CR, Beaudet AL, Sly WS, et al., editors. The metabolic and molecular bases of inherited disease. 8th ed. New York: Mc-Graw-Hill, 2001: 3389–420 Hirschhorn R, Reuser AJJ. Glycogen storage disease type II: acid alpha-glucosidase (acid maltase) deficiency. In: Scriver CR, Beaudet AL, Sly WS, et al., editors. The metabolic and molecular bases of inherited disease. 8th ed. New York: Mc-Graw-Hill, 2001: 3389–420
74.
Zurück zum Zitat Kishnani PS, Howell RR. Pompe disease in infants and children. J Pediatr 2004 May; 144 (5 Suppl.): S35–43PubMedCrossRef Kishnani PS, Howell RR. Pompe disease in infants and children. J Pediatr 2004 May; 144 (5 Suppl.): S35–43PubMedCrossRef
75.
Zurück zum Zitat Gambetti P, DiMauro S, Baker L. Nervous system in Pompe’s disease: ultrastructure and biochemistry. J Neuropathol Exp Neurol 1971 Jul; 30(3): 412–30PubMedCrossRef Gambetti P, DiMauro S, Baker L. Nervous system in Pompe’s disease: ultrastructure and biochemistry. J Neuropathol Exp Neurol 1971 Jul; 30(3): 412–30PubMedCrossRef
76.
Zurück zum Zitat Sakurai I, Tosaka A, Mori Y, et al. Glycogenosis type II (Pompe): the fourth autopsy case in Japan. Acta Pathol Jpn 1974 Nov; 24(6): 829–46PubMed Sakurai I, Tosaka A, Mori Y, et al. Glycogenosis type II (Pompe): the fourth autopsy case in Japan. Acta Pathol Jpn 1974 Nov; 24(6): 829–46PubMed
77.
Zurück zum Zitat Kishnani PS, Hwu WL, Mandel H, et al. A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease. J Pediatr 2006 May; 148(5): 671–6PubMedCrossRef Kishnani PS, Hwu WL, Mandel H, et al. A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease. J Pediatr 2006 May; 148(5): 671–6PubMedCrossRef
78.
Zurück zum Zitat Van den Hout HM, Hop W, van Diggelen OP, et al. The natural course of infantile Pompe’s disease: 20 original cases compared with 133 cases from the literature. Pediatrics 2003 Aug; 112(2): 332–40PubMedCrossRef Van den Hout HM, Hop W, van Diggelen OP, et al. The natural course of infantile Pompe’s disease: 20 original cases compared with 133 cases from the literature. Pediatrics 2003 Aug; 112(2): 332–40PubMedCrossRef
79.
Zurück zum Zitat Jongen SP, Gerwig GJ, Leeflang BR, et al. N-glycans of recombinant human acid alpha-glucosidase expressed in the milk of transgenic rabbits. Glycobiology 2007 Jun; 17(6): 600–19PubMedCrossRef Jongen SP, Gerwig GJ, Leeflang BR, et al. N-glycans of recombinant human acid alpha-glucosidase expressed in the milk of transgenic rabbits. Glycobiology 2007 Jun; 17(6): 600–19PubMedCrossRef
80.
Zurück zum Zitat Bijvoet AG, Van Hirtum H, Kroos MA, et al. Human acid alpha-glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type II. Hum Mol Genet 1999 Nov; 8(12): 2145–53PubMedCrossRef Bijvoet AG, Van Hirtum H, Kroos MA, et al. Human acid alpha-glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type II. Hum Mol Genet 1999 Nov; 8(12): 2145–53PubMedCrossRef
81.
Zurück zum Zitat Van den Hout H, Reuser AJ, Vulto AG, et al. Recombinant human alpha-glucosidase from rabbit milk in Pompe patients. Lancet 2000 Jul 29; 356(9227): 397–8PubMedCrossRef Van den Hout H, Reuser AJ, Vulto AG, et al. Recombinant human alpha-glucosidase from rabbit milk in Pompe patients. Lancet 2000 Jul 29; 356(9227): 397–8PubMedCrossRef
82.
Zurück zum Zitat Van den Hout JM, Reuser AJ, de Klerk JB, et al. Enzyme therapy for pompe disease with recombinant human alpha-glucosidase from rabbit milk. J Inherit Metab Dis 2001 Apr; 24(2): 266–74PubMedCrossRef Van den Hout JM, Reuser AJ, de Klerk JB, et al. Enzyme therapy for pompe disease with recombinant human alpha-glucosidase from rabbit milk. J Inherit Metab Dis 2001 Apr; 24(2): 266–74PubMedCrossRef
83.
Zurück zum Zitat Van den Hout JM, Kamphoven JH, Winkel LP, et al. Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk. Pediatrics 2004 May; 113(5): e448–57PubMedCrossRef Van den Hout JM, Kamphoven JH, Winkel LP, et al. Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk. Pediatrics 2004 May; 113(5): e448–57PubMedCrossRef
84.
Zurück zum Zitat Klinge L, Straub V, Neudorf U, et al. Safety and efficacy of recombinant acid alpha-glucosidase (rhGAA) in patients with classical infantile Pompe disease: results of a phase II clinical trial. Neuromuscul Disord 2005 Jan; 15(1): 24–31PubMedCrossRef Klinge L, Straub V, Neudorf U, et al. Safety and efficacy of recombinant acid alpha-glucosidase (rhGAA) in patients with classical infantile Pompe disease: results of a phase II clinical trial. Neuromuscul Disord 2005 Jan; 15(1): 24–31PubMedCrossRef
85.
Zurück zum Zitat Kishnani PS, Nicolino M, Voit T, et al. Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe disease. J Pediatr 2006 Jul; 149(1): 89–97PubMedCrossRef Kishnani PS, Nicolino M, Voit T, et al. Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe disease. J Pediatr 2006 Jul; 149(1): 89–97PubMedCrossRef
86.
Zurück zum Zitat Amalfitano A, Bengur AR, Morse RP, et al. Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trial. Genet Med 2001 Mar–Apr; 3(2): 132–8PubMed Amalfitano A, Bengur AR, Morse RP, et al. Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trial. Genet Med 2001 Mar–Apr; 3(2): 132–8PubMed
87.
Zurück zum Zitat Kishnani PS, Corzo D, Nicolino M, et al. Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe disease. Neurology 2007 Jan 9; 68(2): 99–109PubMedCrossRef Kishnani PS, Corzo D, Nicolino M, et al. Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe disease. Neurology 2007 Jan 9; 68(2): 99–109PubMedCrossRef
88.
Zurück zum Zitat Schiffmann R, Murray GJ, Treco D, et al. Infusion of alpha-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease. Proc Natl Acad Sci U S A 2000 Jan 4; 97(1): 365–70PubMedCrossRef Schiffmann R, Murray GJ, Treco D, et al. Infusion of alpha-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease. Proc Natl Acad Sci U S A 2000 Jan 4; 97(1): 365–70PubMedCrossRef
89.
Zurück zum Zitat Kakkis ED, Schuchman E, He X, et al. Enzyme replacement therapy in feline mucopolysaccharidosis I. Mol Genet Metab 2001 Mar; 72(3): 199–208PubMedCrossRef Kakkis ED, Schuchman E, He X, et al. Enzyme replacement therapy in feline mucopolysaccharidosis I. Mol Genet Metab 2001 Mar; 72(3): 199–208PubMedCrossRef
90.
Zurück zum Zitat Lachmann RH, te Vruchte D, Lloyd-Evans ER, et al. Treatment with miglustat reverses the lipid-trafficking defect in Niemann-Pick disease type C. Neurobiol Dis 2004 Aug; 16(3): 654–8PubMedCrossRef Lachmann RH, te Vruchte D, Lloyd-Evans ER, et al. Treatment with miglustat reverses the lipid-trafficking defect in Niemann-Pick disease type C. Neurobiol Dis 2004 Aug; 16(3): 654–8PubMedCrossRef
91.
Zurück zum Zitat Russell C, Hendson G, Jevon G, et al. Murine MPS I: insights into the pathogenesis of Hurler syndrome. Clin Genet 1998 May; 53(5): 349–61PubMedCrossRef Russell C, Hendson G, Jevon G, et al. Murine MPS I: insights into the pathogenesis of Hurler syndrome. Clin Genet 1998 May; 53(5): 349–61PubMedCrossRef
92.
Zurück zum Zitat Jeyakumar M, Thomas R, Elliot-Smith E, et al. Central nervous system inflammation is a hallmark of pathogenesis in mouse models of GM1 and GM2 gangliosidosis. Brain 2003 Apr; 126 (Pt 4): 974–87PubMedCrossRef Jeyakumar M, Thomas R, Elliot-Smith E, et al. Central nervous system inflammation is a hallmark of pathogenesis in mouse models of GM1 and GM2 gangliosidosis. Brain 2003 Apr; 126 (Pt 4): 974–87PubMedCrossRef
93.
Zurück zum Zitat Wada R, Tifft CJ, Proia RL. Microglial activation precedes acute neurodegeneration in Sandhoff disease and is suppressed by bone marrow transplantation. Proc Natl Acad Sci U S A 2000 Sep 26; 97(20): 10954–9PubMedCrossRef Wada R, Tifft CJ, Proia RL. Microglial activation precedes acute neurodegeneration in Sandhoff disease and is suppressed by bone marrow transplantation. Proc Natl Acad Sci U S A 2000 Sep 26; 97(20): 10954–9PubMedCrossRef
Metadaten
Titel
Treatment of Lysosomal Storage Disorders
Progress with Enzyme Replacement Therapy
verfasst von
Marianne Rohrbach
Dr Joe T. R. Clarke
Publikationsdatum
01.12.2007
Verlag
Springer International Publishing
Erschienen in
Drugs / Ausgabe 18/2007
Print ISSN: 0012-6667
Elektronische ISSN: 1179-1950
DOI
https://doi.org/10.2165/00003495-200767180-00005

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