Immunoproteomic identification of anti-C9 autoimmune antibody in patients with seronegative obstetric antiphospholipid syndrome
Autor: | Hideo Orimo, Akira Katayama, Toshiyuki Takeshita, Yoshimitsu Kuwabara, Sachiko Kurihara |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
Adult
Male Proteomics 0301 basic medicine lcsh:Medicine Mass Spectrometry Epitope Serology Epitopes 03 medical and health sciences 0302 clinical medicine Antigen Antiphospholipid syndrome Humans Medicine Electrophoresis Gel Two-Dimensional lcsh:Science Autoantibodies 030203 arthritis & rheumatology Multidisciplinary biology business.industry lcsh:R Autoantibody Antiphospholipid Syndrome Complement C9 medicine.disease Blood proteins Primary and secondary antibodies Complement system 030104 developmental biology Immunology biology.protein Female lcsh:Q business Biomarkers |
Zdroj: | PLoS ONE, Vol 13, Iss 6, p e0198472 (2018) |
ISSN: | 1932-6203 |
Popis: | 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. |
Databáze: | OpenAIRE |
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