T-CELL RECEPTOR VARIABLE REGION GENE USAGE BY CD4-CELLS IN BRONCHOALVEOLAR LAVAGE FLUID AND PERIPHERAL-BLOOD OF SARCOIDOSIS PATIENTS( AND CD8+ T)

Citation
J. Grunewald et al., T-CELL RECEPTOR VARIABLE REGION GENE USAGE BY CD4-CELLS IN BRONCHOALVEOLAR LAVAGE FLUID AND PERIPHERAL-BLOOD OF SARCOIDOSIS PATIENTS( AND CD8+ T), Proceedings of the National Academy of Sciences of the United Statesof America, 91(11), 1994, pp. 4965-4969
Citations number
23
Categorie Soggetti
Multidisciplinary Sciences
ISSN journal
00278424
Volume
91
Issue
11
Year of publication
1994
Pages
4965 - 4969
Database
ISI
SICI code
0027-8424(1994)91:11<4965:TRVRGU>2.0.ZU;2-U
Abstract
Sarcoidosis is a chronic noncaseating granulomatous disease of unknown etiology. An accumulation of CD4(+) T cells in the alveolar space of the lungs is a characteristic feature of the disease. We have in this study analyzed T-cell receptor (TCR) variable region (V) gene usage by CD4(+) and CD8(+) lung and peripheral blood T cells of 29 sarcoidosis patients and 15 control subjects. In the patient group, we found a 10 0% positive correlation between TCR V (alpha)2.3(+) CD4(+) lung T-cell expansions and the expression of the HLA-DR3(17),DQ2 haplotype. The r emaining TCR V (alpha)/V (beta) gene products analyzed in this study-V (alpha)12, V (beta)2, V (beta)3, V (beta)5.1, V (beta)5.2/5.3, V (bet a)5.3, V (beta)6.7, V (beta)8.1, and V (beta)12-were in general normal ly expressed by CD4(+) T cells, although some of them were used to a s ignificantly higher or lower degree by lung T cells compared to periph eral blood T cells. We also performed repeated TCR V gene analyses on some HLA-DR3(+) patients and found an association between the ratio br onchoalveolar lavage fluid/peripheral blood V (alpha)2.3(+) CD4(+) T c ells and clinical signs of disease activity. Finally, when analyzing T CR V gene usage by CD8(+) bronchoalveolar lavage fluid and peripheral blood T cells, a normal V (alpha,)2.3 usage was found in all cases, bu t lung-restricted T-cell expansions using other TCR V gene segment pro ducts were identified.