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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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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. |
format | Online Article Text |
id | pubmed-9910615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
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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