HLA A*, B*-BF* and C4 A*, B* allele associations, with special reference to BF*S07, in the Tunisian population

J Immunogenet. 1983 Jun;10(3):205-8. doi: 10.1111/j.1744-313x.1983.tb00796.x.

Abstract

The HLA A*2, Bw*50-BF*S07-C4 A*2, B*1 linkage group was transmitted unambiguously in four unrelated Tunisian families. In one of these, another allele association, also carrying BF*S07, HLA A*9, Bw*50-BF*S07-C4 A*1, B*1, was encountered. The previously reported linkage disequilibrium between BF*S07 and HLA Bw*50, a subtypic specificity of HLA Bw*21, is confirmed in our study. The C4 A*2, B*1 haplotype, rare in the other populations until now studied, seems more frequent in Tunisia since it has been also found linked to HLA A*11, B*27 and BF*S in one of these families. Other allele associations were unambiguously demonstrated with predominantly the C4 A*3, B*1 haplotype, particularly a rare HLA A*3, B*18-BF*F1-C4 A*3, B*1 linkage group. A silent gene at the C4 A locus was found linked to HLA B*8.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Complement C4 / genetics*
  • Complement Factor B / genetics*
  • Enzyme Precursors / genetics*
  • Female
  • Genetic Linkage
  • HLA Antigens / genetics*
  • HLA-A Antigens
  • HLA-B Antigens
  • Humans
  • Male
  • Pedigree
  • Tunisia

Substances

  • Complement C4
  • Enzyme Precursors
  • HLA Antigens
  • HLA-A Antigens
  • HLA-B Antigens
  • Complement Factor B