Source:http://linkedlifedata.com/resource/pubmed/id/16257179
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2005-11-21
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pubmed:databankReference | |
pubmed:abstractText |
Proteoglycan (PG)-induced arthritis (PGIA), a murine model for rheumatoid arthritis (RA), is driven by antigen (PG)-specific T and B cell activation. In order to analyze the pathogenic role of antigen-specific T cells in the development of autoimmune arthritis, we have generated a transgenic (Tg) mouse. The CD4(+) T cells of this TCR-5/4E8-Tg line express a functional T cell receptor (TCR) composed of the Valpha1.1 and Vbeta4 chains with specificity for the dominant arthritogenic T cell epitope of human cartilage PG. Adoptive transfer of naive TCR-5/4E8-Tg cells induced arthritis with severe clinical symptoms in syngeneic immunodeficient BALB/c.RAG2(-/-) mice. In vivo activation of TCR-5/4E8-Tg CD4(+)Vbeta4(+) cells with cartilage PG seemed to be critical for arthritis induction. Arthritis never developed after transfer of naive wild-type cells. The arthritis was characterized as a chronic progressive disease with intermittent spontaneous exacerbations and remissions. Inflamed joints showed extensive cartilage damage and bone erosions leading to massive ankylosis in peripheral joints. These PG epitope-specific TCR-5/4E8-Tg mice can be valuable research tools for studying antigen-driven T cell regulation in arthritis, and migration of T cells to the joints. In addition the model may be used for the development of immune modulating strategies in T cell-mediated autoimmune diseases.
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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 |
Nov
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pubmed:issn |
0896-8411
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
25
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
172-80
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pubmed:meshHeading |
pubmed-meshheading:16257179-Amino Acid Sequence,
pubmed-meshheading:16257179-Animals,
pubmed-meshheading:16257179-Arthritis, Experimental,
pubmed-meshheading:16257179-Cartilage, Articular,
pubmed-meshheading:16257179-Cloning, Molecular,
pubmed-meshheading:16257179-G0 Phase,
pubmed-meshheading:16257179-Gene Transfer Techniques,
pubmed-meshheading:16257179-Humans,
pubmed-meshheading:16257179-Hybridomas,
pubmed-meshheading:16257179-Lymphocyte Activation,
pubmed-meshheading:16257179-Mice,
pubmed-meshheading:16257179-Mice, Inbred BALB C,
pubmed-meshheading:16257179-Mice, Transgenic,
pubmed-meshheading:16257179-Molecular Sequence Data,
pubmed-meshheading:16257179-Proteoglycans,
pubmed-meshheading:16257179-Receptors, Antigen, T-Cell, alpha-beta,
pubmed-meshheading:16257179-T-Lymphocytes
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pubmed:year |
2005
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pubmed:articleTitle |
Naive transgenic T cells expressing cartilage proteoglycan-specific TCR induce arthritis upon in vivo activation.
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pubmed:affiliation |
Department of Infectious Diseases and Immunology, Division of Immunology, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 1, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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