Clinical relevance and HLA association of autoantibodies against the nucleolus organizer region (NOR-90)

J Rheumatol. 1995 Jan;22(1):67-72.

Abstract

Objective: NOR-90 autoantibodies directed against the nucleolus organizer region (NOR) have been described as rare scleroderma associated antibodies. We studied the clinical features of patients with NOR-90 antibodies as well as their HLA phenotype.

Methods: NOR-90 antibodies were detected by indirect immunofluorescence assay using HEp-2 cells, by chromosome spreads as a substrate and in addition by Western blot analysis with HeLa-S3 nucleolar extract. HLA antigens of the NOR-90 antibody positive patients were typed with the standard NIH complement dependent microcytotoxicity test.

Results: Nine sera selected by means of the indirect immunofluorescence revealed a typical double band pattern of about 90 kDa identical with the pattern of 2 NOR-90 reference sera by Western blot analysis. Only one patient positive for NOR-90 antibodies suffered from systemic sclerosis (limited cutaneous scleroderma). The other patients with NOR-90 antibodies showed no signs of systemic sclerosis. All patients with NOR-90 antibodies were women and 8 of 9 patients (89 versus 13% of healthy controls, Pcorr < 0.001) were positive for the HLA-DR1 allele.

Conclusion: In contrast to the first report on NOR-90 antibodies we demonstrated no association of these antibodies with systemic sclerosis; however, we found strong evidence for an immunogenetic background of NOR-90 antibody formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antibodies, Antinuclear / blood*
  • Antibody Specificity
  • Blotting, Western
  • DNA-Binding Proteins / immunology*
  • Female
  • Fluorescent Antibody Technique
  • Humans
  • Middle Aged
  • Nucleolus Organizer Region / immunology*
  • Pol1 Transcription Initiation Complex Proteins*
  • Rheumatic Diseases / immunology
  • Scleroderma, Systemic / blood
  • Scleroderma, Systemic / immunology*
  • Transcription Factors / immunology*

Substances

  • Antibodies, Antinuclear
  • DNA-Binding Proteins
  • Pol1 Transcription Initiation Complex Proteins
  • Transcription Factors
  • transcription factor UBF