1. CD19+ B-cells in autoantibody-negative limbic encephalitis.
- Author
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Hansen N, Önder D, Schwing K, Widman G, Leelaarporn P, Prusseit I, Surges R, Becker AJ, Witt JA, Helmstaedter C, and Elger CE
- Subjects
- Adult, Biomarkers cerebrospinal fluid, Blood-Brain Barrier diagnostic imaging, Blood-Brain Barrier metabolism, Blood-Brain Barrier physiopathology, Electroencephalography methods, Epilepsy, Temporal Lobe diagnostic imaging, Epilepsy, Temporal Lobe physiopathology, Female, Humans, Limbic Encephalitis diagnostic imaging, Limbic Encephalitis physiopathology, Magnetic Resonance Imaging methods, Male, Middle Aged, Neuropsychological Tests, Pilot Projects, Retrospective Studies, Antigens, CD19 cerebrospinal fluid, Autoantibodies cerebrospinal fluid, B-Lymphocytes metabolism, Epilepsy, Temporal Lobe cerebrospinal fluid, Limbic Encephalitis cerebrospinal fluid
- Abstract
Purpose: Flow cytometry helps to elucidate the cellular immune repertoire's mechanisms in patients with temporal lobe epilepsy (TLE) due to limbic encephalitis (LE) subcategories and carries potential significance for subtype-specific treatment., Methods: We enrolled 62 patients with TLE due to LE associated with no autoantibodies (n = 40), neural autoantibodies (n = 22), as well as autoantibodies against intracellular antigens (n = 15/22). All patients underwent neuropsychological testing, brain magnetic resonance imaging (MRI), electroencephalography (EEG) recordings, and peripheral blood (PB) and cerebrospinal fluid (CSF) investigations including flow cytometry., Results: CD19+ B-cells were increased in the PB and CSF of patients with antibody-negative LE compared with those associated with antibodies against intracellular antigens (Kruskal-Wallis one way analysis of variance (ANOVA) on ranks with Dunn's test, p < 0.05). There were no differences in CD138+ B-cells, CD4+ T-cells, human leukocyte antigen - DR isotype (HLA-DR+) CD4+ T-cells, CD8+ T-cells, and HLA-DR+ CD8+ T-cells in the CSF between groups with LE. The blood-brain barrier is more often impaired in patients with antibody-negative LE than in LE with antibodies against intracellular antigens (chi-square test, p < 0.05). In addition, we detected no correlations between immune cell subsets and clinical or paraclinical parameters in patients with antibody-negative and intracellular antibody-positive LE., Conclusions: The increase of CD19+ B-cells in the CSF and frequent signs of dysfunctional blood-brain barrier in patients with antibody-negative rather than intracellular antibody-positive LE suggest that CD19+ B-cells play a role in antibody-negative encephalitis although their pathogenic role in the central nervous system (CNS) immunity because of missing correlations between immune cells and clinical and paraclinical parameters remains unknown. Further studies are required to evaluate the usefulness of these B-cells as a biomarker for the stratification of treatment strategies., Competing Interests: Declaration of competing interest NH, DÖ, GW, KS, JAW, PL, IP, and AJB have no potential conflict of interest to declare. CEE has received speaker and consultant fees from ESAI, Cyberonics, Desitin, Novartis, Union Chimique Belge, and Medtronic. RS reports speaker or consultant fees from Bial, Desitin, Eisai, Liva Nova, Novartis, and UCB, Pharma. CH has received fees as a speaker and consultant from Desitin, Esai, UCB, GW, and Precisis., (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Published
- 2020
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