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Circulating immune complexome analysis identified anti-tubulin-α-1c as an inflammation associated autoantibody with promising diagnostic value for Behcet’s Disease
- Source :
- PLoS ONE, Vol 13, Iss 6, p e0199047 (2018), PLoS ONE
- Publication Year :
- 2018
- Publisher :
- Public Library of Science (PLoS), 2018.
-
Abstract
- Background Behcet's disease (BD) is a chronic, multisystem-involved vasculitis and its pathogenesis remains elusive. No specific serological markers for BD diagnosis have been established. Identification of novel diagnostic biomarkers will be helpful in timely diagnostic and treatment for Behcet's disease. Objective To screen novel autoantigens or autoantibodies with potential diagnostic value in circulating immune complexes (CICs) from BD patients. Methods A proteomic strategy for immune complexome analysis was developed, in which CICs were separated from serum sample of 10 BD patients and 10 healthy controls and then subjected to Orbitrap mass spectrometry for autoantigen profiling. Anti-tubulin-α-1c antibody levels were further determined by enzyme-linked immunosorbent assay (ELISA) in sera of patients with BD, systemic lupus erythematosus (SLE), recurrent aphthous ulcers (RAU), ANCA associated systemic vasculitis (AASV), Takayasu's arteritis (TA) and 59 healthy controls. Result A total of 17 potential antigens were identified in CICs from BD patients, but not in HC. The autoantibody to one of the identified antigens, tubulin-α-1c, was significantly increased in BD patients compared with that in healthy and disease controls. The sensitivity and specificity of tubulin-α-1c antibody in the diagnosis of BD in this study were 61.36% and 88.4%, respectively. Further analysis demonstrated that anti-tubulin-α-1c was associated with complications of deep venous thrombosis and erythema nodosum in BD. The levels of anti-tubulin-α-1c were also significantly correlated with the BD inflammation and disease activity markers ESR, CRP and BVAS. Conclusion Anti-tubulin-α-1c antibody is a promising biomarker in diagnosis and severity evaluation of BD and in indicating the risk of deep venous thrombosis and erythema nodosum. The immune complexome analysis by proteomic CIC autoantigen screening is a feasible way of identifying novel biomarkers in BD.
- Subjects :
- Proteomics
0301 basic medicine
Physiology
lcsh:Medicine
Behcet's disease
Biochemistry
0302 clinical medicine
Tubulin
Immune Physiology
Medicine and Health Sciences
Enzyme-Linked Immunoassays
lcsh:Science
Erythema nodosum
Immune System Proteins
Multidisciplinary
Behcet Syndrome
Biomarker (medicine)
Vasculitis
Research Article
Systemic vasculitis
Inflammatory Diseases
Immunology
Research and Analysis Methods
Systemic Lupus Erythematosus
Antibodies
Autoimmune Diseases
03 medical and health sciences
Rheumatology
Antigen
Diagnostic Medicine
Tubulins
medicine
Humans
Arteritis
Immunoassays
Autoantibodies
Inflammation
030203 arthritis & rheumatology
Lupus Erythematosus
business.industry
lcsh:R
Autoantibody
Biology and Life Sciences
Proteins
medicine.disease
Cytoskeletal Proteins
030104 developmental biology
Immunologic Techniques
Blood Vessels
Clinical Immunology
lcsh:Q
Clinical Medicine
business
Biomarkers
Subjects
Details
- ISSN :
- 19326203
- Volume :
- 13
- Database :
- OpenAIRE
- Journal :
- PLOS ONE
- Accession number :
- edsair.doi.dedup.....390b0b99b9d5fe7a21ebb32a96ca414b