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An altered repertoire of T cell receptor V gene expression by rheumatoid synovial fluid T lymphocytes
SUMMARY The pattern of T cell receptor V gene expression by lymphocytes from rheumatoid synovial fluid and paired peripheral blood samples was compared using a polymerasc chain reaction (PCR)‐based assay. Eight rheumatoid arthritis (RA) patients who had varying durations of disease (from 2 to 20 yea...
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Published in: | Clinical and experimental immunology 1992-12, Vol.90 (3), p.440-446 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | SUMMARY
The pattern of T cell receptor V gene expression by lymphocytes from rheumatoid synovial fluid and paired peripheral blood samples was compared using a polymerasc chain reaction (PCR)‐based assay. Eight rheumatoid arthritis (RA) patients who had varying durations of disease (from 2 to 20 years) were studied. In all patients there was evidence of a different pattern of V gene expression between the two compartments. Significantly increased expression of at least one Vα or Vβ gene family by synovial fluid T cells was observed in all the patients studied. Three different Vα (Vα 10, 15 and 18) and three Vβ (Vβ 4, 5 and 13) families were commonly elevated. Sequencing of synovial Vβ transcripts demonstrated that the basis of increased expression of selected V gene families in the synovial fluid was due to the presence of dominant clonotypes within those families, which constituted up to 53% of the sequences isolated from one particular synovial V gene family. There were considerable differences in the NDJ sequences found in synovial and peripheral blood T cell receptor (TCR) transcripts of the same Vα gene family. These data suggest that the TCR repertoire in the two compartments differs, and that antigen‐driven expansion of particular synovial T cell populations is a component of rheumatoid synovitis, and is present in all stages of the disease. |
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ISSN: | 0009-9104 1365-2249 |
DOI: | 10.1111/j.1365-2249.1992.tb05865.x |