Interleukin-17 mRNA expression in blood and CSF mononuclear cells is augmented in multiple sclerosis

Darius Matusevičius(Karolinska University Hospital), Pia Kivisäkk(Karolinska University Hospital), Bing He(Karolinska University Hospital), Nikolaos Kostulas(Karolinska University Hospital), Volkan Özenci(Karolinska University Hospital), S. Fredrikson(Karolinska University Hospital), Hans Link(Karolinska University Hospital)
Multiple Sclerosis Journal
April 1, 1999
Cited by 740

Abstract

Myelin-directed autoimmunity is considered to play a key role in the pathogenesis of multiple sclerosis (MS). Increased production of both pro- and anti-inflammatory cytokines is a common finding in MS. Interleukin-17 (IL-17) is a recently described cytokine produced in humans almost exclusively by activated memory T cells, which can induce the production of proinflammatory cytokines and chemokines from parenchymal cells and macrophages. In situ hybridisation with synthetic oligonucleotide probes was adopted to detect and enumerate IL-17 mRNA expressing mononuclear cells (MNC) in blood and cerebrospinal fluid (CSF) from patients with MS and control individuals. Numbers of IL-17 mRNA expressing blood MNC were higher in patients with MS and acute aseptic meningoencephalitis (AM) compared to healthy individuals. Higher numbers of IL-17 mRNA expressing blood MNC were detected in MS patients examined during clinical exacerbation compared to remission. Patients with MS had higher numbers of IL-17 mRNA expressing MNC in CSF compared to blood. This increase in numbers of IL-17 mRNA expressing MNC in CSF was not observed in patients with AM. Our results thus demonstrate increased numbers of IL-17 mRNA expressing MNC in MS with higher numbers in CSF than blood, and with the highest numbers in blood during clinical exacerbations.


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