MOLECULAR ANALYSIS OF T-CELL RECEPTOR-BETA VARIABILITY IN A PATIENT WITH OROFACIAL GRANULOMATOSIS

Citation
Sh. Lim et al., MOLECULAR ANALYSIS OF T-CELL RECEPTOR-BETA VARIABILITY IN A PATIENT WITH OROFACIAL GRANULOMATOSIS, Gut, 40(5), 1997, pp. 683-686
Citations number
10
Categorie Soggetti
Gastroenterology & Hepatology
Journal title
GutACNP
ISSN journal
00175749
Volume
40
Issue
5
Year of publication
1997
Pages
683 - 686
Database
ISI
SICI code
0017-5749(1997)40:5<683:MAOTRV>2.0.ZU;2-G
Abstract
Background-Orofacial granulomatosis (OFG) is a rare chronic inflammato ry disorder of unknown causation and is characterised histologically b y non-caseating granulomas and aggregates of small lymphocytes. The mo lecular nature of these T cells is, however, unclear. Aims-To determin e 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-C ompared with peripheral blood lymphocytes from the same patient, notab ly restricted TCRV beta gene usage was observed in the T cell infiltra te. Only three of the 24 major TCRV beta gene families were represente d 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 ant igen 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 wi th a local T cell clonal expansion. The results, therefore, provide a new perspective on the immunopathology of OFG.