<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Grygorczuk S</submitter><funding>Uniwersytet Medyczny w Bialymstoku</funding><pagination>126</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5483307</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Host factors determining the clinical presentation of tick-borne encephalitis (TBE) are not fully elucidated. The peripheral inflammatory response to TBE virus is hypothesized to facilitate its entry into central nervous system by disrupting the blood-brain barrier with the involvement of a signaling route including Toll-like receptor 3 (TLR3) and pro-inflammatory cytokines macrophage migration inhibitory factor (MIF), tumor necrosis factor-α (TNFα), and interleukin-1 beta (IL-1β).&lt;h4>Methods&lt;/h4>Concentrations of MIF, TNFα, and IL-1β were measured with commercial ELISA in serum and cerebrospinal fluid (CSF) from 36 hospitalized TBE patients, 7 patients with non-TBE meningitis, and 6 controls. The CSF albumin quotient (AQ) was used as a marker of blood-brain barrier perm</pubmed_abstract><journal>Journal of neuroinflammation</journal><pubmed_title>The increased concentration of macrophage migration inhibitory factor in serum and cerebrospinal fluid of patients with tick-borne encephalitis.</pubmed_title><pmcid>PMC5483307</pmcid><funding_grant_id>143-45624L</funding_grant_id><funding_grant_id>134-45728L</funding_grant_id><pubmed_authors>Moniuszko A</pubmed_authors><pubmed_authors>Czupryna P</pubmed_authors><pubmed_authors>Parczewski M</pubmed_authors><pubmed_authors>Swierzbinska R</pubmed_authors><pubmed_authors>Dunaj J</pubmed_authors><pubmed_authors>Kondrusik M</pubmed_authors><pubmed_authors>Grygorczuk S</pubmed_authors><pubmed_authors>Pancewicz S</pubmed_authors></additional><is_claimable>false</is_claimable><name>The increased concentration of macrophage migration inhibitory factor in serum and cerebrospinal fluid of patients with tick-borne encephalitis.</name><description>&lt;h4>Background&lt;/h4>Host factors determining the clinical presentation of tick-borne encephalitis (TBE) are not fully elucidated. The peripheral inflammatory response to TBE virus is hypothesized to facilitate its entry into central nervous system by disrupting the blood-brain barrier with the involvement of a signaling route including Toll-like receptor 3 (TLR3) and pro-inflammatory cytokines macrophage migration inhibitory factor (MIF), tumor necrosis factor-α (TNFα), and interleukin-1 beta (IL-1β).&lt;h4>Methods&lt;/h4>Concentrations of MIF, TNFα, and IL-1β were measured with commercial ELISA in serum and cerebrospinal fluid (CSF) from 36 hospitalized TBE patients, 7 patients with non-TBE meningitis, and 6 controls. The CSF albumin quotient (AQ) was used as a marker of blood-brain barrier perm</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jun</publication><modification>2025-04-22T11:39:29.682Z</modification><creation>2019-03-27T02:48:26Z</creation></dates><accession>S-EPMC5483307</accession><cross_references><pubmed>28646884</pubmed><doi>10.1186/s12974-017-0898-2</doi></cross_references></HashMap>