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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007600,
umls-concept:C0009013,
umls-concept:C0023509,
umls-concept:C0039194,
umls-concept:C0205225,
umls-concept:C0334094,
umls-concept:C0542341,
umls-concept:C0871261,
umls-concept:C1159954,
umls-concept:C1280500,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C1707455,
umls-concept:C2911692
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pubmed:issue |
1-2
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pubmed:dateCreated |
1994-10-12
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pubmed:abstractText |
An autoreactive T cell clone derived from a patient with reactive arthritis, two alloreactive T cell lines, two antigen-specific T cell lines and allogeneic resting T cells were analyzed for their responses to monocytes and macrophages derived from monocytes by in vitro differentiation. The autoreactive T cell clone strongly proliferated in response to fresh monocytes and to macrophages derived from a 7 day culture, but only poorly to monocytes cultured for 2 days. In contrast, alloreactive and antigen-specific T cell lines proliferated to all stimulatory cells equally well. Finally, primary mixed lymphocyte reactions could be stimulated by both fresh and 2-day cultured monocytes, but not by in vitro derived macrophages. The impaired response of the autoreactive T cell clone to 2-day cultured monocytes could not be attributed to reduced expression of several well-defined surface molecules nor to induction of nonresponsiveness. Neither allogeneic monocytes nor cytokines (IL-1, IL-2, IL-4, IL-6) could correct the defective response of the autoreactive T cell clone. However, preculture of monocytes in the presence of interferon-gamma, IL-1, IL-4 or IL-6 retained their stimulatory capacity. Our interpretation of the selectively impaired response of the autoreactive T cell clone is that it most likely recognizes a differentiation-dependent monocyte/macrophage-specific peptide.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0171-2985
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
190
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
164-74
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7521857-Antigen-Presenting Cells,
pubmed-meshheading:7521857-Antigens, Surface,
pubmed-meshheading:7521857-Autoantigens,
pubmed-meshheading:7521857-Cell Differentiation,
pubmed-meshheading:7521857-Cell Division,
pubmed-meshheading:7521857-Cell Line,
pubmed-meshheading:7521857-Epitopes,
pubmed-meshheading:7521857-Humans,
pubmed-meshheading:7521857-Isoantigens,
pubmed-meshheading:7521857-Lymphocyte Activation,
pubmed-meshheading:7521857-Lymphocyte Culture Test, Mixed,
pubmed-meshheading:7521857-Monocytes,
pubmed-meshheading:7521857-T-Lymphocyte Subsets
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pubmed:year |
1994
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pubmed:articleTitle |
Monocyte differentiation and accessory function: different effects on the proliferative responses of an autoreactive T cell clone as compared to alloreactive or antigen-specific T cell lines and primary mixed lymphocyte cultures.
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pubmed:affiliation |
Abteilung Rheumatologie, Medizinische Klinik, Freiburg, Germany.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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