PREDOMINANCE OF T-CELL RECEPTOR V-DELTA-3 IN SMALL-BOWEL BIOPSIES FROM CELIAC-DISEASE PATIENTS

Citation
Mc. Falk et al., PREDOMINANCE OF T-CELL RECEPTOR V-DELTA-3 IN SMALL-BOWEL BIOPSIES FROM CELIAC-DISEASE PATIENTS, Clinical and experimental immunology, 98(1), 1994, pp. 78-82
Citations number
32
Categorie Soggetti
Immunology
ISSN journal
00099104
Volume
98
Issue
1
Year of publication
1994
Pages
78 - 82
Database
ISI
SICI code
0009-9104(1994)98:1<78:POTRVI>2.0.ZU;2-0
Abstract
Increased numbers of T cells bearing the gamma delta antigen receptor (gamma delta T cells) have been reported in small bowel biopsies of pa tients with latent, active or treated coeliac disease. We have studied jejunal biopsies from seven children with coeliac disease and 10 chil dren with normal gut histology to characterize gamma delta T cell rece ptor (TCR) variable region gene subfamily expression in resident gamma delta T cells and compared the results with the findings in periphera l blood mononuclear cells (PBMC) obtained on the same day as the gut b iopsy. Molecular analysis of RNA extracted from PBMC and biopsies was performed by reverse transcription and amplification with the polymera se chain reaction using primers specific for six TCR V delta families and four TCR V gamma families. We report, first, that a significantly increased number of gamma delta T cells expressing the TCR V delta 3 s ubfamily (P = 0.008) was observed in jejunal biopsies from children wi th coeliac disease, and second, that gamma delta T cell V region subfa mily populations in gut differed from those seen in PBMC for both cont rol and coeliac patients. Significantly reduced numbers of TCR V delta 2, V delta 3, V delta 5 (P < 0.01) and V gamma 2, V gamma 4 (P < 0.01 ) T cells were found in gut compared with PBMC. The difference in gamm a delta T cell repertoire observed between gut and blood may reflect d ifferences in the nature of the antigens usually encountered in these two compartments. The over-representation of TCR V delta 3 in patients with coeliac disease suggests a specific role for these cells in the induction or maintenance of the jejunal abnormality associated with th is disease.