Oligoclonal myelin-reactive T-cell infiltrates derived from multiple sclerosis lesions are enriched in Th17 cells

In this study, acute and chronic brain and spinal cord lesions, and normal appearing white matter (NAWM), were resected post-mortem from a patient with aggressive relapsing-remitting multiple sclerosis (MS). T-cell infiltrates from the central nervous system (CNS) lesions and NAWM were separated and...

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Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 130(2009), 2 vom: 09. Feb., Seite 133-44
1. Verfasser: Montes, Monica (VerfasserIn)
Weitere Verfasser: Zhang, Xin, Berthelot, Laureline, Laplaud, David-Axel, Brouard, Sophie, Jin, Jianping, Rogan, Sarah, Armao, Diane, Jewells, Valerie, Soulillou, Jean-Paul, Markovic-Plese, Silva
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2009
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Interleukin-17 Receptors, Antigen, T-Cell, alpha-beta Receptors, Cytokine Transcription Factors
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500 |a Date Revised 21.03.2022 
500 |a published: Print-Electronic 
500 |a ErratumIn: Clin Immunol. 2022 Apr;237:108967. - PMID 35307286 
500 |a Citation Status MEDLINE 
520 |a In this study, acute and chronic brain and spinal cord lesions, and normal appearing white matter (NAWM), were resected post-mortem from a patient with aggressive relapsing-remitting multiple sclerosis (MS). T-cell infiltrates from the central nervous system (CNS) lesions and NAWM were separated and characterized in-vitro. All infiltrates showed a proliferative response against multiple myelin peptides. Studies of the T-cell receptor (TCR)Vbeta and Jbeta usage revealed a very skewed repertoire with shared complementarity-determining region (CDR)3 lengths detected in all CNS lesions and NAWM. In the acute lesion, genomic profiling of the infiltrating T-cells revealed up-regulated expression of TCRalpha and beta chain, retinoic acid-related orphan nuclear hormone receptor C (RORC) transcription factor, and multiple cytokine genes that mediate Th17 cell expansion. The differentially expressed genes involved in regulation of Th17 cells represent promising targets for new therapies of relapsing-remitting MS 
650 4 |a Journal Article 
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650 4 |a Research Support, Non-U.S. Gov't 
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700 1 |a Zhang, Xin  |e verfasserin  |4 aut 
700 1 |a Berthelot, Laureline  |e verfasserin  |4 aut 
700 1 |a Laplaud, David-Axel  |e verfasserin  |4 aut 
700 1 |a Brouard, Sophie  |e verfasserin  |4 aut 
700 1 |a Jin, Jianping  |e verfasserin  |4 aut 
700 1 |a Rogan, Sarah  |e verfasserin  |4 aut 
700 1 |a Armao, Diane  |e verfasserin  |4 aut 
700 1 |a Jewells, Valerie  |e verfasserin  |4 aut 
700 1 |a Soulillou, Jean-Paul  |e verfasserin  |4 aut 
700 1 |a Markovic-Plese, Silva  |e verfasserin  |4 aut 
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