Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity

Science. 1995 Jun 2;268(5215):1347-9. doi: 10.1126/science.7539157.

Abstract

Fas (also known as Apo1 and CD95) is a cell surface receptor involved in apoptotic cell death. Fas expression and function were analyzed in three children (including two siblings) with a lymphoproliferative syndrome, two of whom also had autoimmune disorders. A large deletion in the gene encoding Fas and no detectable cell surface expression characterized the most affected patient. Clinical manifestations in the two related patients were less severe: Fas-mediated apoptosis was impaired and a deletion within the intracytoplasmic domain was detected. These findings illustrate the crucial regulatory role of Fas and may provide a molecular basis for some autoimmune diseases in humans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Antigens, Surface / chemistry
  • Antigens, Surface / genetics*
  • Antigens, Surface / physiology
  • Apoptosis
  • Autoimmune Diseases / genetics*
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / pathology
  • Base Sequence
  • Child
  • Female
  • Frameshift Mutation*
  • Humans
  • Infant
  • Lymphoproliferative Disorders / genetics*
  • Lymphoproliferative Disorders / immunology
  • Lymphoproliferative Disorders / pathology
  • Male
  • Molecular Sequence Data
  • Sequence Deletion
  • Syndrome
  • Thrombocytopenia / genetics
  • Thrombocytopenia / immunology
  • Thrombocytopenia / pathology
  • fas Receptor

Substances

  • Antigens, Surface
  • fas Receptor