The pathogenesis of pulmonary sarcoidosis has been related to an increased
production of Th1-like cytokines. However, cytokine expression in sarcoidos
is has not been systematically studied at a single-cell level. We therefore
investigated the expression of IL-2, IL-4, IL-13, tumour necrosis factor-a
lpha (TNF-alpha) and interferon-gamma (IFN-gamma) intracellularly in bronch
oalveolar lavage (BAL) and peripheral blood CD3(+) T lymphocytes from patie
nts with pulmonary sarcoidosis (radiologic stage II-III, n = 8) and normal
controls (n = 9) by flow cytometry. In contrast to IL-4 and IL-13, the perc
entage of T lymphocytes expressing intracellular IL-2 (49.3 +/- 21.3% versu
s 14.5 +/- 15.6%), IFN-gamma (75.5 +/- 14.9% versus 32.6 +/- 18.7%) and TNF
-alpha (68.3 +/- 18.7% versus 36.8 +/- 20.8%) was significantly higher in p
atients with sarcoidosis than in normal controls (each P < 0.005). In contr
ast to BAL lymphocytes, expression of these cytokines in peripheral blood l
ymphocytes did not differ between patients with sarcoidosis and normal cont
rols. Close correlations were observed between the percentages of BAL lymph
ocytes expressing intracellular IL-2, IFN-gamma and TNF-alpha, but not for
IL-4 or IL-13. Analysis of the expression of these cytokines in T lymphocyt
e subsets revealed IL-2, IFN-gamma, and TNF-alpha in CD4(+) as well as CD8(
+) T lymphocytes, suggesting a contribution of TC1 cells to the production
of proinflammatory cytokines in sarcoidosis. We conclude that a Th1-like cy
tokine pattern can be observed in CD4(+) as well as in CD8(+) BAL T lymphoc
ytes in patients with pulmonary sarcoidosis.