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Dominant T cell receptor rearrangements in interleukin 2 expanded lymphocytes from rheumatoid nodules suggest antigen driven T cell activation in situ.

AbstractOBJECTIVE: To study at a molecular level the clonality of interleukin 2 (IL-2) expanded T cell lines derived from rheumatoid nodules. Such cell lines were reported in earlier studies with flow cytometry and antiidiotypic monoclonal antibodies (MAb) to be obligoclonal. METHODS: T cell lines were derived from rheumatoid nodules in 2 patients with rheumatoid arthritis (RA) and expanded in medium containing IL-2. Clonality was assessed by flow cytometry and T cell receptor (TCR) idiotype specific Mab and by polymerase chain reaction with primers for V alpha and V beta gene families. Sequence analysis was performed in selected cell lines. RESULTS: In one patient, one cell line was identified with marked overexpression of V alpha 2 cells. Eleven V alpha 2 CDR3 sequences were derived from this cell line: 8 of these clones had an identical CDR3 sequence and one other clone showed a related sequence. Five cell lines derived from a second patient displayed a marked clonal bias to V beta 8 cells. One cell line with strong V beta 8 expression was chosen for further sequence analysis. Twelve V beta 8 sequences were obtained; 11 showed identical CDR3 sequences. CONCLUSION: Molecular analysis of TCR rearrangements in IL-2 expanded T cell lines from rheumatoid nodules strongly suggests that in situ T cell activation is related to classical antigen induced immune activation.
AuthorsF De Keyser, D Elewaut, J P Overmeer-Graus, P Van den Broek, A W Rijnders, E M Veys (Affiliation: Department of Rheumatology, University Hospital Ghent, Belgium.)
JournalThe Journal of rheumatology (J Rheumatol) Vol. 24 Issue 9 Pg. 1685-9 (Sep 1997) ISSN: 0315-162X CANADA
PMID9292788 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA Primers
  • Interleukin-2
  • Receptors, Antigen, T-Cell, alpha-beta
Topics
  • Aged
  • Arthritis, Rheumatoid (complications)
  • Cell Line
  • Clone Cells (immunology)
  • DNA Primers (chemistry)
  • Flow Cytometry
  • Gene Rearrangement, alpha-Chain T-Cell Antigen Receptor (genetics)
  • Gene Rearrangement, beta-Chain T-Cell Antigen Receptor (genetics)
  • Humans
  • Interleukin-2 (pharmacology)
  • Lymphocyte Activation (drug effects, genetics)
  • Male
  • Polymerase Chain Reaction
  • Receptors, Antigen, T-Cell, alpha-beta (drug effects, genetics, immunology)
  • Rheumatoid Nodule (immunology)
  • T-Lymphocytes (immunology)