Lim, S. H., Stephens, Philip ORCID: https://orcid.org/0000-0002-0840-4996, Cao, Q.X., Coleman, Sharon Louise and Thomas, David ORCID: https://orcid.org/0000-0001-7319-5820 1997. Molecular analysis of T cell receptor beta variability in a patient with orofacial granulomatosis. Gut 40 (5) , pp. 683-686. 10.1136/gut.40.5.683 |
Abstract
BACKGROUND: Orofacial granulomatosis (OFG) is a rare chronic inflammatory disorder of unknown causation and is characterised histologically by non-caseating granulomas and aggregates of small lymphocytes. The molecular nature of these T cells is, however, unclear. AIMS: To determine the T cell receptor (TCR) V beta gene usage of the T cell infiltrate associated with the primary lesions in a patient with OFG. METHODS: A molecular method involving reverse transcriptase (RT)-polymerase chain reaction (PCR), DNA cloning, single strand conformation polymorphism (SSCP), length analysis, and nucleotide sequencing was used. RESULTS: Compared with peripheral blood lymphocytes from the same patient, notably restricted TCRV beta gene usage was observed in the T cell infiltrate. Only three of the 24 major TCRV beta gene families were represented in the repertoire. There was preferential usage of the V beta 6 gene. In addition, more than 20% of the V beta 6 TCR transcripts exhibited an identical unique V-D-J junctional sequence, suggesting a local antigen driven V beta 6 T cell clonal expansion in vivo, a phenomenon not observed in normal oral mucosa. CONCLUSIONS: The TCRV beta repertoire of T cells associated with OFG is restricted. It is also associated with a local T cell clonal expansion. The results, therefore, provide a new perspective on the immunopathology of OFG.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Medicine |
Subjects: | R Medicine > R Medicine (General) |
Publisher: | BMJ Publishing Group |
ISSN: | 0017-5749 |
Last Modified: | 06 Nov 2024 22:26 |
URI: | https://orca.cardiff.ac.uk/id/eprint/60605 |
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