A C77G point mutation in CD45 exon 4, which is associated with the development of multiple sclerosis and increased susceptibility to HIV-1 infection, is undetectable in Japanese population

Eur J Neurol. 2003 Nov;10(6):737-9. doi: 10.1046/j.1468-1331.2003.00679.x.

Abstract

HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP) is one outcome of Human T-cell lymphotropic virus type 1 (HTLV-1) infection. It remains unknown why the majority of infected people remain healthy whereas only approximately 2-3% develop disease. Recently, heterozygous state of CD45 exon 4 mutation (C77C wild type and C77G mutant) was reported to be associated with development of multiple sclerosis in German patients and increased susceptibility to HIV-1 infection in the United Kingdom. To investigate whether this mutation is associated with the development of HAM/TSP, we studied a group of 164 HAM/TSP patients and 108 asymptomatic HTLV-1 carriers in Kagoshima (HTLV-1 endemic area in Southern Japan) by using PCR-RFLP and subsequent direct sequencing analysis. All 272 subjects showed homozygosity in the CD45 exon 4, suggesting that this mutation is absent or very rare in Japanese population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier State
  • Exons / genetics
  • Gene Frequency
  • HIV Infections / genetics*
  • HIV Infections / immunology*
  • Human T-lymphotropic virus 1
  • Humans
  • Japan / epidemiology
  • Leukocyte Common Antigens / genetics*
  • Multiple Sclerosis / genetics*
  • Paraparesis, Tropical Spastic / physiopathology
  • Point Mutation / genetics*
  • Point Mutation / physiology*
  • Polymorphism, Restriction Fragment Length
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Leukocyte Common Antigens
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1