Determination of Gaucher's disease phenotypes with monoclonal antibody

Clin Chim Acta. 1983 Jul 15;131(3):283-7. doi: 10.1016/0009-8981(83)90097-9.

Abstract

Discrimination between the three clinical subtypes of Gaucher's disease based on the molecular forms of beta-glucocerebrosidase detected by monoclonal antibody is described. In normal fibroblast extracts, cross-reacting material (CRM) to human placental glucocerebrosidase is detected at Mr approximately equal to 63 000, 61 000 and 56 000. In Type 1 Gaucher's disease, the major fibroblast CRM has a Mr approximately equal to 56 000,, with less CRM seen at 61 000 and 56 000. Type 3 fibroblast extracts have a single CRM form at Mr approximately equal to 63 000. No CRM is found in Type 2 Gaucher's disease fibroblasts with monoclonal antiglucocerebrosidase antibody 8E4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal
  • Fibroblasts / enzymology
  • Gaucher Disease / diagnosis*
  • Gaucher Disease / genetics
  • Glucosidases / isolation & purification*
  • Glucosylceramidase / immunology
  • Glucosylceramidase / isolation & purification*
  • Humans
  • Immunochemistry
  • Phenotype

Substances

  • Antibodies, Monoclonal
  • Glucosidases
  • Glucosylceramidase