Inui N, Chida K, Suda T, Nakamura H
Second Division, Department of Internal Medicine, Hamamatsu University School of Medicine, Shizuoka, Japan.
J Allergy Clin Immunol. 2001 Feb;107(2):337-44. doi: 10.1067/mai.2001.112273.
Sarcoidosis is thought to be a type-1 cytokine-mediated disorder. However, few data are available on the profiles of cytokine expression by TH cells at the single-cell level, as assessed by intracellular cytokine flow cytometry. Additionally, it remains to be determined whether the balance of TC1 and TC2 cells can be altered in sarcoidosis.
The aim of this study was to evaluate the TH1/TH2 and TC1/TC2 balances in sarcoidosis.
Using triple-color flow cytometry and phorbol 12-myristate acetate/ionomycin stimulation, we measured the production of the intracellular cytokines IFN-gamma and IL-4 in CD4+ and CD8+ T cells separately, which were obtained from peripheral blood and bronchoalveolar lavage fluid (BALF) of 20 patients with sarcoidosis, and compared their cytokine expressions with those of 10 normal subjects.
Under unstimulated conditions, there were no significant differences in the proportion of cytokine-producing CD4+ or CD8+ T cells in peripheral blood or BALF between patients with sarcoidosis and normal control subjects. On stimulation with phorbol 12-myristate acetate/ionomycin for 4 hours, in BALF of the patients, but not in peripheral blood, we found a significant increase in the percentage of IFN-gamma-producing CD4+ T cells and 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 compared with that found in normal subjects. In contrast, no difference was found 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.
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.
结节病被认为是一种1型细胞因子介导的疾病。然而,关于通过细胞内细胞因子流式细胞术评估的单细胞水平TH细胞的细胞因子表达谱的数据很少。此外,结节病中TC1和TC2细胞的平衡是否会改变仍有待确定。
本研究旨在评估结节病中的TH1/TH2和TC1/TC2平衡。
我们使用三色流式细胞术和佛波醇12 - 肉豆蔻酸酯乙酸盐/离子霉素刺激,分别测量了从20例结节病患者的外周血和支气管肺泡灌洗液(BALF)中获得的CD4 +和CD8 + T细胞内细胞因子IFN - γ和IL - 4的产生,并将其细胞因子表达与10名正常受试者的进行比较。
在未刺激条件下,结节病患者和正常对照受试者外周血或BALF中产生细胞因子的CD4 +或CD8 + T细胞比例无显著差异。在用佛波醇12 - 肉豆蔻酸酯乙酸盐/离子霉素刺激4小时后,在患者的BALF中,而非外周血中,我们发现产生IFN - γ的CD4 + T细胞百分比显著增加,产生IL - 4的CD4 + T细胞百分比降低,导致产生IFN - γ/IL - 4的CD4 + T细胞比例比正常受试者高3.5倍。相比之下,患者和正常受试者外周血或BALF中产生细胞因子的CD8 + T细胞比例或产生IFN - γ/IL - 4的CD8 + T细胞比例均无差异。
这些发现表明,在结节病受累器官中,CD4 + T细胞群体可能会显著向1型表型转变,而CD8 + T细胞群体则不会。