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Immunoproteomic identification of anti-C9 autoimmune antibody in patients with seronegative obstetric antiphospholipid syndrome. | LitMetric

AI Article Synopsis

  • The study explored the presence of unknown molecules related to seronegative obstetric antiphospholipid syndrome (APS) by analyzing blood samples from patients who meet the clinical criteria for APS but not the serological criteria.
  • Researchers collected plasma from different groups, including those with and without thrombotic predisposition, and utilized techniques like two-dimensional immunoblotting and mass spectrometry to identify specific proteins associated with the condition.
  • The findings indicated a connection between seronegative APS and autoantibodies that target specific epitopes of the complement molecule C9, revealing potential biomarkers for the disease.

Article Abstract

Immunoproteomic analysis was performed to identify unknown, pathology-related molecules in patients with seronegative (SN) obstetric antiphospholipid syndrome (APS) who clinically satisfied the diagnostic criteria for APS, but not the serological criteria. We collected peripheral blood from 13 SN-APS outpatients with known thrombotic predisposition, 13 with no known thrombotic predisposition, and four multiparous women with no history of miscarriage (control). Plasma proteins from volunteers were purified and used as plasma protein antigens. Two-dimensional immunoblotting was performed using pooled control or SN-APS serum samples as the primary antibodies. Mass spectrometry of reactive spots specific to SN-APS serum led to the identification of complement molecule C9. Western blotting using commercial purified alkylated C9 was performed to detect autoantibodies. Examination of individual patient serum identified reactivity in one patient with, and in two patients without known thrombotic predisposition. This study suggests that SN-APS pathologies were associated with autoantibodies that react to specific C9 epitopes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5997311PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0198472PLOS

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