http://purl.uniprot.org/citations/23599932 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/23599932 | http://www.w3.org/2000/01/rdf-schema#comment | "ObjectiveTo investigate the expression of CD161 (KLRB1) and CCR6 on human γδ T cells in blood and cerebrospinal fluid (CSF) of patients with a clinically isolated syndrome (CIS) and multiple sclerosis (MS) in relapse.DesignFlow cytometry analysis of CD161 and CCR6 expression and intracellular cytokine staining for interleukin 17 and interferon-γ on human γδ T cells in blood and CSF samples.SettingDepartment of Neurology, Klinikum rechts der Isar, Technische Universität München, a tertiary referral center.PatientsTwenty-six patients with CIS/MS in active relapse, 10 patients with other autoimmune disorders, 12 patients with neuroinfectious diseases, and 15 patients with noninflammatory neurological diseases.Main outcome measuresFrequencies of CD161high and CCR6+ γδ T cells in blood and CSF samples of patients with CIS/MS in relapse and control patients.Resultsγδ T cells were increased in both blood and CSF of patients with CIS/MS in relapse as compared with controls with noninflammatory disease. The fraction of CD161high CCR6+ γδ T cells was significantly higher in the CSF of patients with CIS/MS in relapse than of those with systemic autoimmune disorders or controls with noninflammatory disease. The CD161high CCR6+ double-positive γδ T-cell population was further enriched in the CSF in relation to blood in patients with CIS/MS in relapse but not in patients with infectious disease or the other control groups. The CD161high CCR6+ γδ T-cell population was characterized by its capacity to produce interleukin 17.ConclusionInterleukin 17–producing CD161high CCR6+ γδ T cells might contribute to the compartmentalized inflammatory process in the central nervous system of patients with MS."xsd:string |
http://purl.uniprot.org/citations/23599932 | http://purl.org/dc/terms/identifier | "doi:10.1001/2013.jamaneurol.409"xsd:string |
http://purl.uniprot.org/citations/23599932 | http://purl.uniprot.org/core/author | "Hemmer B."xsd:string |
http://purl.uniprot.org/citations/23599932 | http://purl.uniprot.org/core/author | "Korn T."xsd:string |
http://purl.uniprot.org/citations/23599932 | http://purl.uniprot.org/core/author | "Rothhammer V."xsd:string |
http://purl.uniprot.org/citations/23599932 | http://purl.uniprot.org/core/author | "Schirmer L."xsd:string |
http://purl.uniprot.org/citations/23599932 | http://purl.uniprot.org/core/date | "2013"xsd:gYear |
http://purl.uniprot.org/citations/23599932 | http://purl.uniprot.org/core/name | "JAMA Neurol"xsd:string |
http://purl.uniprot.org/citations/23599932 | http://purl.uniprot.org/core/pages | "345-351"xsd:string |
http://purl.uniprot.org/citations/23599932 | http://purl.uniprot.org/core/title | "Enriched CD161high CCR6+ gammadelta T cells in the cerebrospinal fluid of patients with multiple sclerosis."xsd:string |
http://purl.uniprot.org/citations/23599932 | http://purl.uniprot.org/core/volume | "70"xsd:string |
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