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Janoschka, Claudia; Lindner, Maren; Koppers, Nils; Starost, Laura; Liebmann, Marie; Eschborn, Melanie; Schneider-Hohendorf, Tilman; Windener, Farina; Schafflick, David; Fleck, Ann-Katrin; Koch, Kathrin; Deffner, Marie; Schwarze, Anna-Sophie; Schulte-Mecklenbeck, Andreas; Metz, Imke; Meuth, Sven G; Gross, Catharina C; Meyer Zu Hörste, Gerd; Schwab, Nicholas; Kuhlmann, Tanja; Wiendl, Heinz; Stoll, Monika; Klotz, Luisa
Proceedings of the National Academy of Sciences - PNAS, 01/2023, Letnik: 120, Številka: 1Journal Article
After natalizumab (NAT) cessation, some multiple sclerosis (MS) patients experience a severe disease rebound. The rebound pathophysiology is still unclear; however, it has been linked to interleukin-17-producing T-helper (Th17) cells. We demonstrate that during NAT treatment, MCAM+CCR6+Th17 cells gradually acquire a pathogenic profile, including proinflammatory cytokine production, pathogenic transcriptional signatures, brain endothelial barrier impairment, and oligodendrocyte damage via induction of apoptotic pathways. This is accompanied by an increase in Th17 cell frequencies in the cerebrospinal fluid of NAT-treated patients. Notably, Th17 cells derived from NAT-treated patients, who later developed a disease rebound upon treatment cessation, displayed a distinct transcriptional pathogenicity profile associated with altered migratory properties. Accordingly, increased brain infiltration of patient Th17 cells was illustrated in a humanized mouse model and brain histology from a rebound patient. Therefore, peripheral blood-accumulated MCAM+CCR6+Th17 cells might be involved in rebound pathophysiology, and monitoring of changes in Th17 cell pathogenicity in patients before/during NAT treatment cessation might enable rebound risk assessment in the future.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Vir: Osebne bibliografije
in: SICRIS
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