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Anti-topoisomerase II alpha autoantibodies in systemic sclerosis-association with pulmonary hypertension and HLA-B35.

Abstract
We have previously detected autoantibodies against topoisomerase II alpha (anti-topo II alpha) in sera from patients with idiopathic pulmonary fibrosis. To determine whether anti-topo II alpha is also present in systemic sclerosis (SSc) patients with pulmonary involvement, we screened sera from 92 patients and 34 healthy controls. Presence of anti-topo II alpha was investigated with respect to clinical and serological features, including the frequencies of HLA class I and II alleles. Anti-topo II alpha was detected in 20/92 (21.7%) patients. No association was found with either anti-topoisomerase I (Scl-70 or anti-topo I) or anti-centromere antibodies. However, anti-topo II alpha was associated with the presence of pulmonary hypertension (PHT) (as opposed to pulmonary fibrosis), and with a decrease of carbon monoxide diffusing capacity. Anti-topo II alpha was strongly associated with the presence of the class I antigen HLA-B35. No significant association was found with HLA class II antigens. HLA-B35 also turned out to be associated with the presence of PHT. These results indicate that in SSc patients, the presence of anti-topo II alpha is associated with PHT, and that the simultaneous presence of HLA-B35 seems to add to the risk of developing PHT.
AuthorsB Grigolo, I Mazzetti, R Meliconi, S Bazzi, R Scorza, M Candela, A Gabrielli, A Facchini
JournalClinical and experimental immunology (Clin Exp Immunol) Vol. 121 Issue 3 Pg. 539-43 (Sep 2000) ISSN: 0009-9104 [Print] England
PMID10971522 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Autoantibodies
  • HLA-B35 Antigen
  • DNA Topoisomerases, Type II
Topics
  • Adult
  • Alleles
  • Autoantibodies (blood)
  • Case-Control Studies
  • DNA Topoisomerases, Type II (immunology)
  • Female
  • HLA-B35 Antigen (genetics)
  • Humans
  • Hypertension, Pulmonary (etiology, genetics, immunology)
  • Male
  • Middle Aged
  • Risk Factors
  • Scleroderma, Systemic (complications, genetics, immunology)

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