IL-6 in the Cerebrospinal Fluid Signals Disease Activity in Multiple Sclerosis.

MS diagnosis MS prognosis cerebrospinal fluid cytokines interleukin-6 multiple sclerosis progressive relapsing–remitting

Journal

Frontiers in cellular neuroscience
ISSN: 1662-5102
Titre abrégé: Front Cell Neurosci
Pays: Switzerland
ID NLM: 101477935

Informations de publication

Date de publication:
2020
Historique:
received: 17 02 2020
accepted: 14 04 2020
entrez: 14 7 2020
pubmed: 14 7 2020
medline: 14 7 2020
Statut: epublish

Résumé

Specific proinflammatory and anti-inflammatory molecules could represent useful cerebrospinal fluid (CSF) biomarkers to predict the clinical course of multiple sclerosis (MS). The proinflammatory molecule interleukin (IL)-6 has been investigated in the pathophysiology of MS and has been associated in previous smaller studies to increased disability and disease activity. Here, we wanted to further address IL-6 as a possible CSF biomarker of MS by investigating its detectability in a large cohort of 534 MS patients and in 103 individuals with other non-inflammatory neurological diseases. In these newly diagnosed patients, we also explored correlations between IL-6 detectability, MS phenotypes, and disease characteristics. We found that IL-6 was more frequently detectable in the CSF of MS patients compared with their control counterparts as significant differences emerged between patients with Clinically isolated syndrome (CIS), Relapsing-remitting (RR), and secondary progressive and primary progressive MS compared to non-inflammatory controls. IL-6 was equally present in the CSF of all MS phenotypes. In RR MS patients, IL-6 detectability was found to signal clinically and/or radiologically defined disease activity, among all other clinical characteristics. Our results add further evidence that CSF proinflammatory cytokines could be useful for the identification of those MS patients who are prone to increased disease activity. In particular, IL-6 could represent an interesting prognostic biomarker of MS, as also demonstrated in other diseases where CSF IL-6 was found to identify patients with worse disease severity.

Identifiants

pubmed: 32655367
doi: 10.3389/fncel.2020.00120
pmc: PMC7324533
doi:

Types de publication

Journal Article

Langues

eng

Pagination

120

Informations de copyright

Copyright © 2020 Stampanoni Bassi, Iezzi, Drulovic, Pekmezovic, Gilio, Furlan, Finardi, Marfia, Sica, Centonze and Buttari.

Références

Nat Rev Neurol. 2012 Nov 5;8(11):647-56
pubmed: 23007702
J Neurol. 2018 Nov;265(11):2540-2547
pubmed: 30167879
Brain. 2008 Jan;131(Pt 1):288-303
pubmed: 18056737
Lancet Neurol. 2018 Feb;17(2):162-173
pubmed: 29275977
J Immunol. 1991 Jul 1;147(1):117-23
pubmed: 2051017
Int J Clin Exp Med. 2015 Sep 15;8(9):16658-63
pubmed: 26629199
Neurology. 1983 Nov;33(11):1444-52
pubmed: 6685237
J Neurosci. 2009 Mar 18;29(11):3442-52
pubmed: 19295150
Nature. 2006 May 11;441(7090):231-4
pubmed: 16648837
Ann Neurol. 2012 Jan;71(1):76-83
pubmed: 22275254
J Neurol Sci. 1997 Feb 27;146(1):59-65
pubmed: 9077497
J Neuroimmunol. 2017 Apr 15;305:175-181
pubmed: 28100408
Nature. 2006 May 11;441(7090):235-8
pubmed: 16648838
Immunity. 2006 Feb;24(2):179-89
pubmed: 16473830
J Neurosci. 1995 Nov;15(11):7095-104
pubmed: 7472464
Front Aging Neurosci. 2018 Aug 08;10:238
pubmed: 30135651
Biochem J. 1990 Feb 1;265(3):621-36
pubmed: 1689567
PLoS One. 2013 Apr 18;8(4):e61835
pubmed: 23637915
J Syst Integr Neurosci. 2017 May;3(3):
pubmed: 28966794
Int Rev Immunol. 1998;16(3-4):249-84
pubmed: 9505191
Mult Scler. 2016 Oct;22(11):1405-1412
pubmed: 26733422
J Neuroinflammation. 2014 Feb 18;11:32
pubmed: 24548694
Mult Scler. 2015 Oct;21(11):1443-52
pubmed: 25583841
J Neuroimmunol. 1991 Apr;32(1):67-74
pubmed: 2002092
Eur J Neurol. 2002 Jul;9(4):413-8
pubmed: 12099927
Med Sci Monit. 2000 Nov-Dec;6(6):1104-8
pubmed: 11208463
Mult Scler. 2018 Apr;24(4):432-439
pubmed: 29512406
J Neuroinflammation. 2016 Nov 24;13(1):297
pubmed: 27881137
Exp Gerontol. 2011 Feb-Mar;46(2-3):199-206
pubmed: 20869430
Mult Scler Relat Disord. 2017 May;14:12-15
pubmed: 28619424
Cytokine. 2016 Jan;77:227-37
pubmed: 26463515
Eur J Immunol. 2010 Jul;40(7):1830-5
pubmed: 20583029

Auteurs

Mario Stampanoni Bassi (M)

Unit of Neurology and Neurorehabilitation, IRCCS Neuromed, Pozzilli, Italy.

Ennio Iezzi (E)

Unit of Neurology and Neurorehabilitation, IRCCS Neuromed, Pozzilli, Italy.

Jelena Drulovic (J)

Clinic of Neurology, Clinical Center of Serbia, Belgrade, Serbia.
Faculty of Medicine, University of Belgrade, Belgrade, Serbia.

Tatjana Pekmezovic (T)

Faculty of Medicine, Institute of Epidemiology, University of Belgrade, Belgrade, Serbia.

Luana Gilio (L)

Unit of Neurology and Neurorehabilitation, IRCCS Neuromed, Pozzilli, Italy.

Roberto Furlan (R)

Clinical Neuroimmunology Unit, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.

Annamaria Finardi (A)

Clinical Neuroimmunology Unit, Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.

Girolama Alessandra Marfia (GA)

Unit of Neurology and Neurorehabilitation, IRCCS Neuromed, Pozzilli, Italy.
Multiple Sclerosis Clinical and Research Unit, Department of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.

Francesco Sica (F)

Unit of Neurology and Neurorehabilitation, IRCCS Neuromed, Pozzilli, Italy.

Diego Centonze (D)

Unit of Neurology and Neurorehabilitation, IRCCS Neuromed, Pozzilli, Italy.
Synaptic Immunopathology Lab, Department of Systems Medicine, Tor Vergata University, Rome, Italy.

Fabio Buttari (F)

Unit of Neurology and Neurorehabilitation, IRCCS Neuromed, Pozzilli, Italy.

Classifications MeSH