Genetic studies in Sjögren's syndrome and systemic lupus erythematosus

J Autoimmun. 1989 Aug;2(4):403-13. doi: 10.1016/0896-8411(89)90169-8.

Abstract

HLA associations with Sjögren's syndrome (SS), previously defined by serologic HLA typing, are reviewed. Because the SS-A/Ro and SS-B/La autoantibody responses in SS and systemic lupus erythematosus (SLE) show even stronger correlations with HLA alleles, HLA-DR and DQ alleles were examined using restriction fragment length polymorphisms (RFLP) in white and black patients with SS and/or SS having anti-Ro and anti-La antibodies. The strongest associations across ethnic lines were with HLA-DR3, DQw2 and DQw1.2 (DQw6), especially the DQw1.2 (DQw6)/Dqw2 heterozygous state. HLA-DQw3 was relatively decreased. These data suggest that HLA-DQ is most likely responsible for these abnormal autoantibody responses. In addition, multiplex family studies of Ro antibodies demonstrates the requirement for both HLA and non-MHC effects.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Antibodies / genetics
  • Antibodies, Antinuclear / genetics
  • Autoantibodies / genetics
  • Autoimmune Diseases / genetics*
  • Disease Susceptibility
  • Female
  • HLA-D Antigens / genetics
  • Humans
  • Lupus Erythematosus, Systemic / genetics*
  • Male
  • Polymorphism, Restriction Fragment Length
  • Racial Groups
  • Sjogren's Syndrome / genetics*

Substances

  • Antibodies
  • Antibodies, Antinuclear
  • Autoantibodies
  • HLA-D Antigens
  • SS-A antibodies