Thrombophilia Associated with Anti-DFS70 Autoantibodies

PLoS One. 2015 Sep 23;10(9):e0138671. doi: 10.1371/journal.pone.0138671. eCollection 2015.

Abstract

Context: Anti-DFS70 antibodies are the most frequent antinuclear antibodies (ANA) found in healthy individuals. We assessed the clinical significance of the presence of anti-DFS70 antibodies.

Methods: We defined a group of patients (n = 421) with anti-DFS70 antibodies and a group of patients (n = 63) with a history of idiopathic arterial and/or venous thrombotic disease and/or obstetric complication (i.e. ≥ 3 miscarriages, fetal death or premature birth with eclampsia). Anti-DFS70 antibodies prevalence was also assessed in a cohort of 300 healthy blood donors.

Results: The prevalence of thrombotic disease and/or obstetric complication in the 421 patients with anti-DFS70 antibodies was 13.1% (n = 55) and the prevalence of connective tissue disease was 19% (n = 80). Among the 63 patients with a history of thrombosis and/or obstetric complications, 7 (11.1%) had anti-DFS70 antibodies and among the latter, 5 had no common thrombophilic factor. In contrast, the prevalence of anti-DFS70 antibodies was of 3.0% (9 out of 300) in healthy donors. Finally, the Activated Partial Thromboplastin Time (aPTT) ratio of patients with a history of thrombosis and anti-DFS70 antibodies was lower than the aPTT ratio of other patients, suggesting that thrombotic patients with anti-DFS70 antibodies may have a hypercoagulable state.

Conclusion: We described here for the first time an immune procoagulant state involving anti-DFS70 antibodies.

MeSH terms

  • Adaptor Proteins, Signal Transducing / immunology*
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Autoantibodies / blood*
  • Autoantibodies / immunology
  • Cohort Studies
  • Connective Tissue Diseases / epidemiology
  • Connective Tissue Diseases / pathology
  • Female
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • Male
  • Middle Aged
  • Partial Thromboplastin Time
  • Prevalence
  • Thrombophilia / epidemiology
  • Thrombophilia / pathology*
  • Thrombosis / pathology
  • Transcription Factors / immunology*
  • Young Adult

Substances

  • Adaptor Proteins, Signal Transducing
  • Autoantibodies
  • PSIP1 protein, human
  • Transcription Factors

Grants and funding

The authors have no support or funding to report.