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231223s2009 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2008.08.030
|2 doi
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|a pubmed24n0614.xml
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|a (DE-627)NLM184221935
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|a (NLM)18977698
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Montes, Monica
|e verfasserin
|4 aut
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|a Oligoclonal myelin-reactive T-cell infiltrates derived from multiple sclerosis lesions are enriched in Th17 cells
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|c 2009
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 27.01.2009
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|a Date Revised 21.03.2022
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|a published: Print-Electronic
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|a ErratumIn: Clin Immunol. 2022 Apr;237:108967. - PMID 35307286
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|a Citation Status MEDLINE
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|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
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|a Journal Article
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|a Research Support, N.I.H., Extramural
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|a Research Support, Non-U.S. Gov't
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|a Interleukin-17
|2 NLM
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|a Receptors, Antigen, T-Cell, alpha-beta
|2 NLM
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|a Receptors, Cytokine
|2 NLM
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|a Transcription Factors
|2 NLM
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|a Zhang, Xin
|e verfasserin
|4 aut
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|a Berthelot, Laureline
|e verfasserin
|4 aut
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|a Laplaud, David-Axel
|e verfasserin
|4 aut
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1 |
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|a Brouard, Sophie
|e verfasserin
|4 aut
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1 |
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|a Jin, Jianping
|e verfasserin
|4 aut
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1 |
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|a Rogan, Sarah
|e verfasserin
|4 aut
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1 |
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|a Armao, Diane
|e verfasserin
|4 aut
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1 |
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|a Jewells, Valerie
|e verfasserin
|4 aut
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1 |
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|a Soulillou, Jean-Paul
|e verfasserin
|4 aut
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1 |
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|a Markovic-Plese, Silva
|e verfasserin
|4 aut
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0 |
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 130(2009), 2 vom: 09. Feb., Seite 133-44
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:130
|g year:2009
|g number:2
|g day:09
|g month:02
|g pages:133-44
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|u http://dx.doi.org/10.1016/j.clim.2008.08.030
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