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Enhanced pathogenicity of Th17 cells due to natalizumab treatment: Implications for MS disease rebound

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 gr...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910615/
https://www.ncbi.nlm.nih.gov/pubmed/36574650
http://dx.doi.org/10.1073/pnas.2209944120
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author 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
author_facet 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
author_sort Janoschka, Claudia
collection PubMed
description 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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spelling pubmed-99106152023-02-10 Enhanced pathogenicity of Th17 cells due to natalizumab treatment: Implications for MS disease rebound 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 Proc Natl Acad Sci U S A Biological Sciences 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. National Academy of Sciences 2022-12-27 2023-01-03 /pmc/articles/PMC9910615/ /pubmed/36574650 http://dx.doi.org/10.1073/pnas.2209944120 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
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
Enhanced pathogenicity of Th17 cells due to natalizumab treatment: Implications for MS disease rebound
title Enhanced pathogenicity of Th17 cells due to natalizumab treatment: Implications for MS disease rebound
title_full Enhanced pathogenicity of Th17 cells due to natalizumab treatment: Implications for MS disease rebound
title_fullStr Enhanced pathogenicity of Th17 cells due to natalizumab treatment: Implications for MS disease rebound
title_full_unstemmed Enhanced pathogenicity of Th17 cells due to natalizumab treatment: Implications for MS disease rebound
title_short Enhanced pathogenicity of Th17 cells due to natalizumab treatment: Implications for MS disease rebound
title_sort enhanced pathogenicity of th17 cells due to natalizumab treatment: implications for ms disease rebound
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910615/
https://www.ncbi.nlm.nih.gov/pubmed/36574650
http://dx.doi.org/10.1073/pnas.2209944120
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