Morquio's disease type A: absence of material cross reacting with antibodies against N-acetylgalactosamine-6-sulfate sulfatase
- PMID: 6156114
- DOI: 10.1007/BF00279054
Morquio's disease type A: absence of material cross reacting with antibodies against N-acetylgalactosamine-6-sulfate sulfatase
Abstract
An antiserum was raised in guinea pigs against purified normal human N-acetylgalactosamine-6-sulfate sulfatase, the enzyme affecting in Morquio's disease type A. The antiserum precipitated most of N-acetylgalactosamine-6-sulfate sulfatase from a concentrate of normal human urine. The antigen-antibody complex was enzymatically active. Urine concentrates from five patients with Morquio's disease type A did not contain material competing with the normal enzyme for binding to soluble or Sepharose-bound antibodies. No precipitin arc was obtained on immunodiffusion of antiserum and urine from the single patient investigated by this method. From the sensitivity of the indirect immunoassay it was concluded that the urine of the five patients contained less than 5% of the normal amount of cross-reacting material.
Similar articles
-
A sensitive procedure for the diagnosis of N-acetyl-galactosamine-6-sulfate sulfatase deficiency in classical Morquio's disease.Clin Chim Acta. 1978 Aug 15;88(1):111-9. doi: 10.1016/0009-8981(78)90157-2. Clin Chim Acta. 1978. PMID: 98244
-
Activities of N-acetylgalactosamine-6-sulfate sulfatase in liver from two sisters with morquio syndrome.Tohoku J Exp Med. 1980 May;131(1):53-7. doi: 10.1620/tjem.131.53. Tohoku J Exp Med. 1980. PMID: 6773185
-
N-acetylgalactosamine-6-sulfate sulfatase in man. Absence of the enzyme in Morquio disease.J Clin Invest. 1976 Apr;57(4):1036-40. doi: 10.1172/JCI108345. J Clin Invest. 1976. PMID: 820716 Free PMC article.
-
Morquio's syndrome. A case report and review of clinical findings.N Y State Dent J. 1998 Oct;64(8):48-50. N Y State Dent J. 1998. PMID: 9828617 Review.
-
[Morquio disease (Mucopolysaccharidosis type IV-A): clinical aspects, diagnosis and new treatment with enzyme replacement therapy].Arch Argent Pediatr. 2015 Aug;113(4):359-64. doi: 10.5546/aap.2015.359. Arch Argent Pediatr. 2015. PMID: 26172013 Review. Spanish.
Cited by
-
Review: the immunochemical analysis of enzyme from mucopolysaccharidoses patients.J Inherit Metab Dis. 1993;16(1):3-15. doi: 10.1007/BF00711309. J Inherit Metab Dis. 1993. PMID: 8487500 Review.
-
Hunter syndrome: presence of material cross-reacting with antibodies against iduronate sulfatase.Hum Genet. 1987 Mar;75(3):234-8. doi: 10.1007/BF00281065. Hum Genet. 1987. PMID: 3104200