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Novel cerebrospinal fluid and serum autoantibody targets for clinically isolated syndrome
Authors:Myrthe Rouwette  Klaartje Somers  Cindy Govarts  Peter P De Deyn  Raymond Hupperts  Bart Van Wijmeersch  Brigit A De Jong  Marcel M Verbeek  Vincent Van Pesch  Christian Sindic  Luisa M Villar  José C Álvarez‐Cermeño  Piet Stinissen  Veerle Somers
Institution:1. Hasselt University, Biomedical Research Institute (BIOMED) and transnationale Universiteit Limburg, School of Life Sciences, , Diepenbeek, Belgium;2. Department of Neurology, Middelheim Hospital, , Antwerp, Belgium;3. Laboratory of Neurochemistry and Behaviour, Department of Biomedical Sciences, Institute Born Bunge, University of Antwerp, , Antwerp, Belgium;4. Department of Neurology, University Medical Center Groningen, , Groningen, The Netherlands;5. School of Mental Health and Neuroscience, Maastricht University Medical Center, , Maastricht, the Netherlands;6. Department of Neurology, Orbis Medical Center, , Sittard, The Netherlands;7. Multiple Sclerosis and Rehabilitation Center, , Overpelt, Belgium;8. MS Centre Nijmegen (MSCN) and Department of Neurology, Radboud University Medical Centre, , Nijmegen, The Netherlands;9. Departments of Neurology and Laboratory Medicine, Radboud University Medical Center, , Nijmegen, The Netherlands;10. Department of Neurology, Cliniques Universitaires St‐Luc, Université Catholique de Louvain, , Brussels, Belgium;11. Departments of Neurology and Immunology, Ramón y Cajal Hospital, , Madrid, Spain
Abstract:Limited information is available on the identity of antigens targeted by antibodies present in cerebrospinal fluid (CSF) of patients with clinically isolated syndrome (CIS). The aim of this study was to identify novel antigens for CIS and investigate their prognostic potential to predict conversion to multiple sclerosis (MS). We applied serological antigen selection (SAS) to identify antigens interacting with antibodies present in the pooled CSF from four CIS patients, who developed MS. Antibody reactivity towards CIS antigens identified by SAS was tested in CSF and serum from patients with CIS (= 123/= 108), MS (= 65/= 44), and other (inflammatory) neurological diseases (= 75/= 38) as well as in healthy control sera (= 44). Using SAS, a panel of six novel CIS candidate antigens was identified. CSF antibody reactivity was detected in both CIS and relapsing‐remitting (RR) MS. Serum reactivity was significantly increased in CIS and RR‐MS as compared with controls (= 0.03). For two antigens, the frequency of antibody‐positive patients was higher in CIS patients who converted to MS as compared with CIS patients without conversion. We identified novel CIS antigens to which antibody reactivity was primarily detected in CIS and RR‐MS as compared to controls. Possible prognostic potential could be demonstrated for two antigens.
Keywords:autoantibody  biomarker  clinically isolated syndrome  multiple sclerosis  serological antigen selection
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