A deletion in the gene encoding the CD45 antigen in a patient with SCID

J Immunol. 2001 Jan 15;166(2):1308-13. doi: 10.4049/jimmunol.166.2.1308.

Abstract

SCID is a heterogeneous group of hereditary diseases. Mutations in the common gamma-chain (gamma(c)) of cytokine receptors, including those for IL-2, IL-4, IL-7, IL-9, and IL-15, are responsible for an X-linked form of the disease, while mutations of several other genes, including Janus-associated kinase-3, may cause autosomal recessive forms of SCID. We investigated the first SCID patient to be described with minimal cell surface expression of the leukocyte common (CD45) Ag. CD45 is an abundant transmembrane tyrosine phosphatase, expressed on all leukocytes, and is required for efficient lymphocyte signaling. CD45-deficient mice are severely immunodeficient and have very few peripheral T lymphocytes. We report here that a homozygous 6-bp deletion in the gene encoding CD45 (PTPRC, gene map locus 1q31-32), which results in a loss of glutamic acid 339 and tyrosine 340 in the first fibronectin type III module of the extracellular domain of CD45, is associated with failure of surface expression of CD45 and SCID. Molecular modeling suggests that tyrosine 340 is crucial for the structural integrity of CD45 protein. This is the second description of a clinically relevant CD45 mutation, provides direct evidence for the importance of CD45 in immune function in humans, and suggests that abnormalities in CD45 expression are a possible cause of SCID in humans.

Publication types

  • Case Reports

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • CHO Cells
  • Cell Line
  • Cell Membrane / genetics
  • Cell Membrane / immunology
  • Cell Membrane / metabolism
  • Cricetinae
  • Female
  • Fibronectins / genetics
  • Glutamic Acid / genetics
  • Humans
  • Infant
  • Leukocyte Common Antigens / biosynthesis
  • Leukocyte Common Antigens / chemistry
  • Leukocyte Common Antigens / genetics*
  • Mice
  • Molecular Sequence Data
  • Polymorphism, Genetic
  • Protein Structure, Tertiary / genetics
  • Sequence Deletion / immunology*
  • Severe Combined Immunodeficiency / diagnosis
  • Severe Combined Immunodeficiency / ethnology
  • Severe Combined Immunodeficiency / genetics*
  • Severe Combined Immunodeficiency / immunology*
  • Transfection
  • Tumor Cells, Cultured
  • Tyrosine / chemistry
  • Tyrosine / genetics

Substances

  • Fibronectins
  • Glutamic Acid
  • Tyrosine
  • Leukocyte Common Antigens