| pubmed-article:8552189 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8552189 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
| pubmed-article:8552189 | lifeskim:mentions | umls-concept:C0014070 | lld:lifeskim |
| pubmed-article:8552189 | lifeskim:mentions | umls-concept:C0014063 | lld:lifeskim |
| pubmed-article:8552189 | lifeskim:mentions | umls-concept:C0030956 | lld:lifeskim |
| pubmed-article:8552189 | lifeskim:mentions | umls-concept:C0243071 | lld:lifeskim |
| pubmed-article:8552189 | lifeskim:mentions | umls-concept:C1517004 | lld:lifeskim |
| pubmed-article:8552189 | pubmed:issue | 6563 | lld:pubmed |
| pubmed-article:8552189 | pubmed:dateCreated | 1996-2-22 | lld:pubmed |
| pubmed-article:8552189 | pubmed:abstractText | Following induction of experimental encephalomyelitis with a T-cell clone, L10C1, that is specific for the myelin basic protein epitope p87-99, the inflammatory infiltrate in the central nervous system contains a diverse collection of T cells with heterogeneous receptors. We show here that when clone L10C1 is tolerized in vivo with an analogue of p87-99, established paralysis is reversed, inflammatory infiltrates regress, and the heterogeneous T-cell infiltrate disappears from the brain, with only the T-cell clones that incited disease remaining in the original lesions. We found that antibody raised against interleukin-4 reversed the tolerance induced by the altered peptide ligand. Treatment with this altered peptide ligand selectively silences pathogenic T cells and actively signals for the efflux of other T cells recruited to the site of disease as a result of the production of interleukin-4 and the reduction of tumour-necrosis factor-alpha in the lesion. | lld:pubmed |
| pubmed-article:8552189 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8552189 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8552189 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8552189 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8552189 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:8552189 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:8552189 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8552189 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:8552189 | pubmed:issn | 0028-0836 | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:MartinRR | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:MitchellDD | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:LindKK | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:FathmanC GCG | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:SteinmanLL | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:GaurAA | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:FerberII | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:UtzUU | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:GijbelsKK | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:FairchildP... | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:O'GarraAA | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:AllegrettaMM | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:BrockeSS | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:WraithD CDC | lld:pubmed |
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| pubmed-article:8552189 | pubmed:author | pubmed-author:ConlonPP | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:VeromaaTT | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:KarinNN | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:WaismanAA | lld:pubmed |
| pubmed-article:8552189 | pubmed:author | pubmed-author:PierceWW | lld:pubmed |
| pubmed-article:8552189 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8552189 | pubmed:day | 25 | lld:pubmed |
| pubmed-article:8552189 | pubmed:volume | 379 | lld:pubmed |
| pubmed-article:8552189 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8552189 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8552189 | pubmed:pagination | 343-6 | lld:pubmed |
| pubmed-article:8552189 | pubmed:dateRevised | 2009-9-29 | lld:pubmed |
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| pubmed-article:8552189 | pubmed:year | 1996 | lld:pubmed |
| pubmed-article:8552189 | pubmed:articleTitle | Treatment of experimental encephalomyelitis with a peptide analogue of myelin basic protein. | lld:pubmed |
| pubmed-article:8552189 | pubmed:affiliation | Department of Neurology and Neurological Sciences, Stanford University Medical Center, California 94305, USA. | lld:pubmed |
| pubmed-article:8552189 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8552189 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:8552189 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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