Disease severity in patients with systemic lupus erythematosus correlates with an increased ratio of interleukin-10:Interferon-gamma-secreting cells in the peripheral blood

被引:267
作者
Hagiwara, E
Gourley, MF
Lee, S
Klinman, DM
机构
[1] US FDA,CTR BIOL EVALUAT & RES,DIV VIRAL PROD,BETHESDA,MD 20892
[2] NIAMSD,NIH,BETHESDA,MD 20892
来源
ARTHRITIS AND RHEUMATISM | 1996年 / 39卷 / 03期
关键词
D O I
10.1002/art.1780390305
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To compare the phenotype and frequency of cells that actively secrete type 1 and type 2 cytokines in systemic lupus erythematosus (SLE) patients (n = 46), versus normal controls (n = 60). Methods. ELISPOT analysis of freshly isolated peripheral blood mononuclear cells (PBMC). Results. T cells were the major source of interleukin-2 (IL-2), IL-4, and interferon-gamma (IFN gamma), whereas monocytes were the primary source of IL-6 and IL-10 in the PB of lupus patients. Significantly fewer PBMC spontaneously secreted IFN gamma and IL-2 (P less than or equal to 0.03), while significantly more PBMC produced IL-6 and IL-10 (P < 0.001), in lupus patients versus controls. Disease severity in lupus patients correlated with an elevated ratio of IL-10:IFN gamma-secreting cells (P < 0.001). Conclusion. SLE is characterized by an imbalance in the ratio of type 1:type 2 cytokine-secreting PBMC.
引用
收藏
页码:379 / 385
页数:7
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