N. Inui et al., T(H)1/T(H)2 and T(C)1/T(C)2 profiles in peripheral blood and bronchoalveolar lavage fluid cells in pulmonary sarcoidosis, J ALLERG CL, 107(2), 2001, pp. 337-344
Background: Sarcoidosis is thought to be a type-1 cytokine-mediated disorde
r. However, few data are available on the profiles of cytokine expression b
y TH cells at the single-cell level, as assessed by intracellular cytokine
now cytometry. Additionally, it remains to be determined whether the balanc
e of T(C)1 and T(C)2 cells can be altered in sarcoidosis.
Objective: The aim of this study was to evaluate the T(H)1/T(H)2 and T(C)1/
T(C)2 balances in sarcoidosis.
Methods: Using triple-color flow cytometry and phorbol 12-myristate acetate
/ionomycin stimulation, we measured the production of the intracellular cyt
okines IFN-gamma and IL-4 in CD4(+) and CD8(+) T cells separately, which we
re obtained from peripheral blood and bronchoalveolar lavage fluid (BALF) o
f 20 patients with sarcoidosis, and compared their cytokine expressions wit
h those of 10 normal subjects.
Results: Under unstimulated conditions, there were no significant differenc
es in the proportion of cytokine-producing CD4(+) or CD8(+) T cells in peri
pheral blood or BALF between patients with sarcoidosis and normal control s
ubjects. On stimulation with phorbol 12-myristate acetate/ionomycin for 4 h
ours, in BALF of the patients, but not in peripheral blood, we found a sign
ificant increase in the percentage of IFN-gamma -producing CD4(+) T cells a
nd a decrease in the percentage of IL-4-producing CD4(+) T cells, resulting
in a 3.5-fold higher ratio of IFN-gamma /IL-4-producing CD4(+) T cells com
pared with that found in normal subjects. In contrast, no difference was fo
und in the proportions of cytokine-producing CD8(+) T cells or the ratio of
IFN-gamma /IL-4-producing CD8(+) T cells in either the peripheral blood or
BALF between the patients and normal subjects.
Conclusions: These findings suggest that the prominent shift toward a type-
1 phenotype may occur in CD4(+) T-cell populations but not in CD8(+) T-cell
populations in the affected organs of sarcoidosis.