Abstract
IL-17 has been implicated in the pathogenesis of multiple sclerosis (MS). Here, we show that blockade of IL-17A, but not IL-17F, attenuated experimental autoimmune encephalomyelitis (EAE). We further show that IL-17A levels were elevated in the CSF of relapsing-remitting MS (RRMS) patients and that they correlated with the CSF/serum albumin quotient (Qalb), a measure of blood-brain barrier (BBB) dysfunction. We then demonstrated that the combination of IL-17A and IL-6 reduced the expression of tight junction (TJ)-associated genes and disrupted monolayer integrity in the BBB cell line hCMEC/D3. However, unlike IL-17A, IL-6 in the CSF from RRMS patients did not correlate with Qalb. These data highlight the potential importance of targeting IL-17A in preserving BBB integrity in RRMS.
Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Aged
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Animals
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Blood-Brain Barrier*
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Cells, Cultured
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Encephalomyelitis, Autoimmune, Experimental / physiopathology*
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Encephalomyelitis, Autoimmune, Experimental / therapy
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Endothelial Cells / drug effects
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Endothelial Cells / metabolism
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Female
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Humans
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Immunization, Passive
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Interleukin-17 / antagonists & inhibitors
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Interleukin-17 / cerebrospinal fluid
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Interleukin-17 / physiology*
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Interleukin-6 / pharmacology
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Mice
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Mice, Inbred C57BL
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Middle Aged
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Multiple Sclerosis, Relapsing-Remitting / cerebrospinal fluid
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Multiple Sclerosis, Relapsing-Remitting / physiopathology*
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Receptors, Interleukin-6 / physiology
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Recombinant Proteins / pharmacology
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Young Adult
Substances
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IL17A protein, human
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IL17F protein, human
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IL6 protein, human
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Il17a protein, mouse
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Interleukin-17
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Interleukin-6
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Receptors, Interleukin-6
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Recombinant Proteins