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Urokinase, CX3CL1, CCL2, TRAIL and IL-18 induced by interferon-β treatment
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- Zhukovsky, Christina (author)
- Uppsala universitet,Landtblom: Neurovetenskap
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- Herman, Stephanie (author)
- Uppsala universitet,Klinisk kemi
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- Wiberg, Anna (author)
- Uppsala universitet,Klinisk immunologi
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- 2021-02-24
- 2021
- English.
- In: Acta Neurologica Scandinavica. - : John Wiley & Sons. - 0001-6314 .- 1600-0404. ; 143:6, s. 602-607
- Journal article (peer-reviewed)
Abstract
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- ObjectiveTo identify serum proteins associated with MS and affected by interferon beta treatment.MethodsPlasma samples from 29 untreated relapsing-remitting MS patients and 15 healthy controls were investigated with a multiplexed panel containing 92 proteins related to inflammation. Follow-up samples were available from 13 patients at 1 and 3 months after initiation of treatment with interferon beta-1a.ResultsTen proteins were differentially expressed in MS patients. Five of these were altered by treatment with IFN-β 1a: uPA, CX3CL1, CCL2, TRAIL and IL18.ConclusionCCL2 and TRAIL were confirmed to be modulated with interferon beta treatment in MS. As novel findings, we now report that uPA and CX3CL1 were differentially expressed in MS and increased after IFN-beta-1a treatment. Conflicting results have been reported on how interferon beta affects IL-18.
Subject headings
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Neurologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Neurology (hsv//eng)
Keyword
- interferon beta
- multiple sclerosis
- TRAIL
- urokinase
Publication and Content Type
- ref (subject category)
- art (subject category)
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