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pubmed-article:15476240pubmed:abstractTextSystemic lupus erythematosus (SLE) is characterized by the existence of a heterogeneous group of autoantibodies directed against intact nuclear structures, such as nucleosomes. The most prominent of these autoantibodies are those directed against double-stranded DNA (dsDNA) and histones. The majority are of the IgG isotype and show affinity maturation, both of which are known hallmarks of T cell help. Much evidence suggests that the nucleosome is a major candidate autoantigen in SLE. In this study, a novel strategy was used to identify the critical CD4+ T cell autoepitopes in nucleosomes. In addition, peptide-based therapy was then performed in a lupus animal model.lld:pubmed
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pubmed-article:15476240pubmed:authorpubmed-author:ChiangBor-Lue...lld:pubmed
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pubmed-article:15476240pubmed:authorpubmed-author:TsaiBor-YuBYlld:pubmed
pubmed-article:15476240pubmed:copyrightInfoCopyright 2004 American College of Rheumatologylld:pubmed
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pubmed-article:15476240pubmed:volume50lld:pubmed
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pubmed-article:15476240pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:15476240pubmed:year2004lld:pubmed
pubmed-article:15476240pubmed:articleTitleTreatment of murine lupus using nucleosomal T cell epitopes identified by bone marrow-derived dendritic cells.lld:pubmed
pubmed-article:15476240pubmed:affiliationKaoshiung Medical University, Kaoshiung, Taiwan, Republic of China.lld:pubmed
pubmed-article:15476240pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15476240pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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