Increased interferon-gamma (IFN-γ), IL-10 and decreased IL-4 mRNA expression in peripheral blood mononuclear cells (PBMC) from patients with systemic lupus erythematosus (SLE)

被引:133
|
作者
Csiszár, A
Nagy, G
Gergely, P
Pozsonyi, T
Pócsik, É
机构
[1] Semmelweis Univ, Fac Med, Dept Internal Med 3, H-1085 Budapest, Hungary
[2] Semmelweis Univ, Cent Immunol Lab, H-1085 Budapest, Hungary
[3] Semmelweis Univ, Natl Inst Haematol & Immunol, H-1085 Budapest, Hungary
来源
CLINICAL AND EXPERIMENTAL IMMUNOLOGY | 2000年 / 122卷 / 03期
关键词
systemic lupus erythematosus; interferon-gamma; IL-10; IL-4; cytokine;
D O I
10.1046/j.1365-2249.2000.01369.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytokines are important regulators of lymphocyte function in SLE. However, the profile of Th1 and Th2 cytokines produced by circulating lymphocytes in human SLE has not been clearly elucidated. The aim of the present study was to characterize the gene expressions of the Th1-type cytokine IFN-gamma, and the Th2-type cytokines IL-10 and IL-4 in PBMC of 15 patients with SLE and 10 healthy individuals by a semiquantitative reverse transcriptase polymerase chain reaction (RT-PCR). Our results showed that expression of IFN-gamma (P = 0.0004) and IL-10 (P = 0.002) transcripts were significantly increased in PBMC of patients with SLE compared with healthy controls. By contrast, expression of IL-4 transcripts in PBMC of patients with SLE was significantly decreased compared with the healthy controls (P = 0.0008). Primary sources of IL-10 were B cells and monocytes, with variable contribution of T cells as detected in various fractions of PBMC of patients with SLE (P = 0.049). These findings support the hypothesis that the enhanced production of IFN-gamma by mononuclear cells may trigger inflammatory responses, together with the enhanced production of IL-10 resulting in autoantibody production by B cells in human SLE.
引用
收藏
页码:464 / 470
页数:7
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