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CD8(+) T-cell pathogenicity in Rasmussen encephalitis elucidated by large-scale T-cell receptor sequencing
Rasmussen encephalitis (RE) is a rare paediatric epilepsy with uni-hemispheric inflammation and progressive neurological deficits. To elucidate RE immunopathology, we applied T-cell receptor (TCR) sequencing to blood (n=23), cerebrospinal fluid (n=2) and brain biopsies (n=5) of RE patients, and paed...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822013/ https://www.ncbi.nlm.nih.gov/pubmed/27040081 http://dx.doi.org/10.1038/ncomms11153 |
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author | Schneider-Hohendorf, Tilman Mohan, Hema Bien, Christian G. Breuer, Johanna Becker, Albert Görlich, Dennis Kuhlmann, Tanja Widman, Guido Herich, Sebastian Elpers, Christiane Melzer, Nico Dornmair, Klaus Kurlemann, Gerhard Wiendl, Heinz Schwab, Nicholas |
author_facet | Schneider-Hohendorf, Tilman Mohan, Hema Bien, Christian G. Breuer, Johanna Becker, Albert Görlich, Dennis Kuhlmann, Tanja Widman, Guido Herich, Sebastian Elpers, Christiane Melzer, Nico Dornmair, Klaus Kurlemann, Gerhard Wiendl, Heinz Schwab, Nicholas |
author_sort | Schneider-Hohendorf, Tilman |
collection | PubMed |
description | Rasmussen encephalitis (RE) is a rare paediatric epilepsy with uni-hemispheric inflammation and progressive neurological deficits. To elucidate RE immunopathology, we applied T-cell receptor (TCR) sequencing to blood (n=23), cerebrospinal fluid (n=2) and brain biopsies (n=5) of RE patients, and paediatric controls. RE patients present with peripheral CD8(+) T-cell expansion and its strength correlates with disease severity. In addition, RE is the only paediatric epilepsy with prominent T-cell expansions in the CNS. Consistently, common clones are shared between RE patients, who also share MHC-I alleles. Public RE clones share Vβ genes and length of the CDR3. Rituximab/natalizumab/basiliximab treatment does not change TCR diversity, stem cell transplantation replaces the TCR repertoire with minimal overlap between donor and recipient, as observed in individual cases. Our study supports the hypothesis of an antigen-specific attack of peripherally expanded CD8(+) lymphocytes against CNS structures in RE, which might be ameliorated by restricting access to the CNS. |
format | Online Article Text |
id | pubmed-4822013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48220132016-04-17 CD8(+) T-cell pathogenicity in Rasmussen encephalitis elucidated by large-scale T-cell receptor sequencing Schneider-Hohendorf, Tilman Mohan, Hema Bien, Christian G. Breuer, Johanna Becker, Albert Görlich, Dennis Kuhlmann, Tanja Widman, Guido Herich, Sebastian Elpers, Christiane Melzer, Nico Dornmair, Klaus Kurlemann, Gerhard Wiendl, Heinz Schwab, Nicholas Nat Commun Article Rasmussen encephalitis (RE) is a rare paediatric epilepsy with uni-hemispheric inflammation and progressive neurological deficits. To elucidate RE immunopathology, we applied T-cell receptor (TCR) sequencing to blood (n=23), cerebrospinal fluid (n=2) and brain biopsies (n=5) of RE patients, and paediatric controls. RE patients present with peripheral CD8(+) T-cell expansion and its strength correlates with disease severity. In addition, RE is the only paediatric epilepsy with prominent T-cell expansions in the CNS. Consistently, common clones are shared between RE patients, who also share MHC-I alleles. Public RE clones share Vβ genes and length of the CDR3. Rituximab/natalizumab/basiliximab treatment does not change TCR diversity, stem cell transplantation replaces the TCR repertoire with minimal overlap between donor and recipient, as observed in individual cases. Our study supports the hypothesis of an antigen-specific attack of peripherally expanded CD8(+) lymphocytes against CNS structures in RE, which might be ameliorated by restricting access to the CNS. Nature Publishing Group 2016-04-04 /pmc/articles/PMC4822013/ /pubmed/27040081 http://dx.doi.org/10.1038/ncomms11153 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Schneider-Hohendorf, Tilman Mohan, Hema Bien, Christian G. Breuer, Johanna Becker, Albert Görlich, Dennis Kuhlmann, Tanja Widman, Guido Herich, Sebastian Elpers, Christiane Melzer, Nico Dornmair, Klaus Kurlemann, Gerhard Wiendl, Heinz Schwab, Nicholas CD8(+) T-cell pathogenicity in Rasmussen encephalitis elucidated by large-scale T-cell receptor sequencing |
title | CD8(+) T-cell pathogenicity in Rasmussen encephalitis elucidated by large-scale T-cell receptor sequencing |
title_full | CD8(+) T-cell pathogenicity in Rasmussen encephalitis elucidated by large-scale T-cell receptor sequencing |
title_fullStr | CD8(+) T-cell pathogenicity in Rasmussen encephalitis elucidated by large-scale T-cell receptor sequencing |
title_full_unstemmed | CD8(+) T-cell pathogenicity in Rasmussen encephalitis elucidated by large-scale T-cell receptor sequencing |
title_short | CD8(+) T-cell pathogenicity in Rasmussen encephalitis elucidated by large-scale T-cell receptor sequencing |
title_sort | cd8(+) t-cell pathogenicity in rasmussen encephalitis elucidated by large-scale t-cell receptor sequencing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822013/ https://www.ncbi.nlm.nih.gov/pubmed/27040081 http://dx.doi.org/10.1038/ncomms11153 |
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