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

Citation
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
Citations number
35
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Immunology
Journal title
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
ISSN journal
00916749 → ACNP
Volume
107
Issue
2
Year of publication
2001
Pages
337 - 344
Database
ISI
SICI code
0091-6749(200102)107:2<337:TATPIP>2.0.ZU;2-K
Abstract
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.