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Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients

Hegen, Harald and Adrianto, Indra and Lessard, Christopher J. and Millonig, Alban and Bertolotto, Antonio and Comabella, Manuel and Giovannoni, Gavin and Guger, Michael and Hoelzl, Martina and Khalil, Michael and Fazekas, Franz and Killestein, Joep and Lindberg, Raija L.P. and Malucchi, Simona and Mehling, Matthias and Montalban, Xavier and Rudzki, Dagmar and Schautzer, Franz and Sellebjerg, Finn and Sorensen, Per Soelberg and Deisenhammer, Florian and Steinman, Lawrence and Axtell, Robert C.. (2016) Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients. Neurol Neuroimmunol Neuroinflamm, 3 (2). e202.

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Official URL: https://edoc.unibas.ch/62323/

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Abstract

OBJECTIVE: To evaluate serum cytokine profiles for their utility to determine the heterogeneous responses to interferon (IFN)-beta treatment in patients with multiple sclerosis (MS). METHODS: Patients with relapsing-remitting MS (RRMS) or clinically isolated syndrome receiving de novo IFN-beta treatment were included in this prospective, observational study. Number of relapses and changes in disability were assessed 2 years prior to and 2 years after initiation of treatment. Sera were collected at baseline and after 3 months on therapy. Cytokine levels in sera were assessed by Luminex multiplex assays. Baseline cytokine profiles were grouped by hierarchical clustering analysis. Demographic features, changes in cytokines, and clinical outcome were then assessed in the clustered patient groups. RESULTS: A total of 157 patients were included in the study and clustered into 6 distinct subsets by baseline cytokine profiles. These subsets differed significantly in their clinical and biological response to IFN-beta therapy. Two subsets were associated with patients who responded poorly to therapy. Two other subsets, associated with a good response to therapy, showed a significant reduction in relapse rates and no worsening of disability. Each subset also had differential changes in cytokine levels after 3 months of IFN-beta treatment. CONCLUSIONS: There is heterogeneity in the immunologic pathways of the RRMS population, which correlates with IFN-beta response.
Faculties and Departments:03 Faculty of Medicine > Departement Biomedizin > Department of Biomedicine, University Hospital Basel > Clinical Neuroimmunology (Derfuss/Lindberg)
03 Faculty of Medicine > Departement Biomedizin > Department of Biomedicine, University Hospital Basel > Translational Neuroimmunology (Mehling)
UniBasel Contributors:Lindberg Gasser, Raija L.P. and Mehling, Matthias
Item Type:Article, refereed
Article Subtype:Research Article
Publisher:Wolters Kluwer Health, Inc.
e-ISSN:2332-7812
Note:Publication type according to Uni Basel Research Database: Journal article
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Last Modified:11 Sep 2018 18:20
Deposited On:24 Apr 2018 15:51

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