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Transcriptomics and proteomics reveal a cooperation between interferon and T-helper 17 cells in neuromyelitis optica

Type I interferon (IFN-I) and T helper 17 (TH17) drive pathology in neuromyelitis optica spectrum disorder (NMOSD) and in TH17-induced experimental autoimmune encephalomyelitis (TH17-EAE). This is paradoxical because the prevalent theory is that IFN-I inhibits TH17 function. Here we report that a ca...

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Autores principales: Agasing, Agnieshka M., Wu, Qi, Khatri, Bhuwan, Borisow, Nadja, Ruprecht, Klemens, Brandt, Alexander Ulrich, Gawde, Saurabh, Kumar, Gaurav, Quinn, James L., Ko, Rose M., Mao-Draayer, Yang, Lessard, Christopher J., Paul, Friedemann, Axtell, Robert C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275086/
https://www.ncbi.nlm.nih.gov/pubmed/32503977
http://dx.doi.org/10.1038/s41467-020-16625-7
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author Agasing, Agnieshka M.
Wu, Qi
Khatri, Bhuwan
Borisow, Nadja
Ruprecht, Klemens
Brandt, Alexander Ulrich
Gawde, Saurabh
Kumar, Gaurav
Quinn, James L.
Ko, Rose M.
Mao-Draayer, Yang
Lessard, Christopher J.
Paul, Friedemann
Axtell, Robert C.
author_facet Agasing, Agnieshka M.
Wu, Qi
Khatri, Bhuwan
Borisow, Nadja
Ruprecht, Klemens
Brandt, Alexander Ulrich
Gawde, Saurabh
Kumar, Gaurav
Quinn, James L.
Ko, Rose M.
Mao-Draayer, Yang
Lessard, Christopher J.
Paul, Friedemann
Axtell, Robert C.
author_sort Agasing, Agnieshka M.
collection PubMed
description Type I interferon (IFN-I) and T helper 17 (TH17) drive pathology in neuromyelitis optica spectrum disorder (NMOSD) and in TH17-induced experimental autoimmune encephalomyelitis (TH17-EAE). This is paradoxical because the prevalent theory is that IFN-I inhibits TH17 function. Here we report that a cascade involving IFN-I, IL-6 and B cells promotes TH17-mediated neuro-autoimmunity. In NMOSD, elevated IFN-I signatures, IL-6 and IL-17 are associated with severe disability. Furthermore, IL-6 and IL-17 levels are lower in patients on anti-CD20 therapy. In mice, IFN-I elevates IL-6 and exacerbates TH17-EAE. Strikingly, IL-6 blockade attenuates disease only in mice treated with IFN-I. By contrast, B-cell-deficiency attenuates TH17-EAE in the presence or absence of IFN-I treatment. Finally, IFN-I stimulates B cells to produce IL-6 to drive pathogenic TH17 differentiation in vitro. Our data thus provide an explanation for the paradox surrounding IFN-I and TH17 in neuro-autoimmunity, and may have utility in predicting therapeutic response in NMOSD.
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spelling pubmed-72750862020-06-16 Transcriptomics and proteomics reveal a cooperation between interferon and T-helper 17 cells in neuromyelitis optica Agasing, Agnieshka M. Wu, Qi Khatri, Bhuwan Borisow, Nadja Ruprecht, Klemens Brandt, Alexander Ulrich Gawde, Saurabh Kumar, Gaurav Quinn, James L. Ko, Rose M. Mao-Draayer, Yang Lessard, Christopher J. Paul, Friedemann Axtell, Robert C. Nat Commun Article Type I interferon (IFN-I) and T helper 17 (TH17) drive pathology in neuromyelitis optica spectrum disorder (NMOSD) and in TH17-induced experimental autoimmune encephalomyelitis (TH17-EAE). This is paradoxical because the prevalent theory is that IFN-I inhibits TH17 function. Here we report that a cascade involving IFN-I, IL-6 and B cells promotes TH17-mediated neuro-autoimmunity. In NMOSD, elevated IFN-I signatures, IL-6 and IL-17 are associated with severe disability. Furthermore, IL-6 and IL-17 levels are lower in patients on anti-CD20 therapy. In mice, IFN-I elevates IL-6 and exacerbates TH17-EAE. Strikingly, IL-6 blockade attenuates disease only in mice treated with IFN-I. By contrast, B-cell-deficiency attenuates TH17-EAE in the presence or absence of IFN-I treatment. Finally, IFN-I stimulates B cells to produce IL-6 to drive pathogenic TH17 differentiation in vitro. Our data thus provide an explanation for the paradox surrounding IFN-I and TH17 in neuro-autoimmunity, and may have utility in predicting therapeutic response in NMOSD. Nature Publishing Group UK 2020-06-05 /pmc/articles/PMC7275086/ /pubmed/32503977 http://dx.doi.org/10.1038/s41467-020-16625-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Agasing, Agnieshka M.
Wu, Qi
Khatri, Bhuwan
Borisow, Nadja
Ruprecht, Klemens
Brandt, Alexander Ulrich
Gawde, Saurabh
Kumar, Gaurav
Quinn, James L.
Ko, Rose M.
Mao-Draayer, Yang
Lessard, Christopher J.
Paul, Friedemann
Axtell, Robert C.
Transcriptomics and proteomics reveal a cooperation between interferon and T-helper 17 cells in neuromyelitis optica
title Transcriptomics and proteomics reveal a cooperation between interferon and T-helper 17 cells in neuromyelitis optica
title_full Transcriptomics and proteomics reveal a cooperation between interferon and T-helper 17 cells in neuromyelitis optica
title_fullStr Transcriptomics and proteomics reveal a cooperation between interferon and T-helper 17 cells in neuromyelitis optica
title_full_unstemmed Transcriptomics and proteomics reveal a cooperation between interferon and T-helper 17 cells in neuromyelitis optica
title_short Transcriptomics and proteomics reveal a cooperation between interferon and T-helper 17 cells in neuromyelitis optica
title_sort transcriptomics and proteomics reveal a cooperation between interferon and t-helper 17 cells in neuromyelitis optica
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275086/
https://www.ncbi.nlm.nih.gov/pubmed/32503977
http://dx.doi.org/10.1038/s41467-020-16625-7
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