Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/50032
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dc.contributor.authorBrian W. Biegleren_US
dc.contributor.authorShirley X. Yanen_US
dc.contributor.authorSterling B. Ortegaen_US
dc.contributor.authorDeepani K. Tennakoonen_US
dc.contributor.authorMichael K. Rackeen_US
dc.contributor.authorNitin J. Karandikaren_US
dc.date.accessioned2018-09-04T04:22:20Z-
dc.date.available2018-09-04T04:22:20Z-
dc.date.issued2011-05-01en_US
dc.identifier.issn01655728en_US
dc.identifier.other2-s2.0-79955666022en_US
dc.identifier.other10.1016/j.jneuroim.2011.02.001en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79955666022&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/50032-
dc.description.abstractPatients with multiple sclerosis (MS) show a high prevalence of myelin-reactive CD8+ and CD4+ T-cell responses, which are the putative effectors/modulators of CNS neuropathology. Utilizing a novel combination of short-term culture, CFSE-based sorting and anchored PCR, we evaluated clonal compositions of neuroantigen-targeting T-cells from RRMS patients and controls. CDR3 region analysis of TCRβ chains revealed biased use of specific TCRBV-bearing CD4+ clones. CD8+ clones showed homology to published TCR from CNS-infiltrating T-cells in MS lesions. These studies are the first description of TCR usage of CNS-specific CD8+ T-cells and provide insights into their potential regulatory role in disease. © 2011 Elsevier B.V.en_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.subjectNeuroscienceen_US
dc.titleClonal composition of neuroantigen-specific CD8+ and CD4+ T-cells in multiple sclerosisen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Neuroimmunologyen_US
article.volume234en_US
article.stream.affiliationsUT Southwestern Medical Schoolen_US
article.stream.affiliationsOhio State University Medical Centeren_US
article.stream.affiliationsChiang Mai Universityen_US
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