Vasilev Georgi, Vasileva Viktoria, Ivanova Mariana, Stanilova Spaska, Manolova Irena, Miteva Lyuba
Laboratory of Hematopathology and Immunology, National Specialized Hospital for Active Treatment of Hematological Diseases, Plovdivsko Pole Str. No. 6, 1756 Sofia, Bulgaria.
Medical Faculty, Sofia University St. Kliment Ohridski, 1 Kozyak Str., 1407 Sofia, Bulgaria.
Curr Issues Mol Biol. 2024 Mar 20;46(3):2644-2657. doi: 10.3390/cimb46030167.
We aimed to investigate the expression of pro-inflammatory cytokine genes , , , , and immunoregulatory genes , , and in the peripheral blood of patients with rheumatoid arthritis (RA) at messenger ribonucleic acid (mRNA) level. The total RNA was isolated from peripheral blood samples. Real-time quantitative PCR was used to perform TaqMan-based assays to quantify mRNAs from 8 target genes. was upregulated (1.7-fold), whereas (5-fold), (4-fold), and (2.56-fold) were downregulated in patients compared to controls. In addition, we found a strong positive correlation between the expression of and and a moderate correlation between and These data showed the imbalance of the T helper (Th) 1/Th17/ T regulatory (Treg) axis at a systemic level in RA. In cases with active disease, the gene expression was approximately 2-fold higher; in contrast, the expression of was significantly decreased (3.38-fold). The main part of patients with higher disease activity expressed upregulation of and downregulation of . Different disease activity cohorts could be separated based on , and expression combinations. In conclusion, our results showed that active disease is associated with an elevated and lower mRNA level in peripheral blood cells of RA patients.
我们旨在研究类风湿关节炎(RA)患者外周血中促炎细胞因子基因、、、、以及免疫调节基因、和在信使核糖核酸(mRNA)水平的表达情况。从外周血样本中分离总RNA。采用实时定量PCR进行基于TaqMan的分析,以定量8个靶基因的mRNA。与对照组相比,患者中上调(1.7倍),而、(5倍)、(4倍)和(2.56倍)下调。此外,我们发现和的表达之间存在强正相关,和之间存在中度相关。这些数据表明,RA患者在系统水平上T辅助(Th)1/Th17/调节性T(Treg)轴失衡。在疾病活动期患者中,基因表达约高2倍;相反,的表达显著降低(3.38倍)。疾病活动度较高的患者主要表现为上调和下调。基于、和的表达组合可以区分不同疾病活动度队列。总之,我们的结果表明,疾病活动与RA患者外周血细胞中升高和较低的mRNA水平相关。