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类风湿关节炎患者外周血白细胞介素-23和类风湿因子的表达研究 被引量:7

The study of interleukin-23 and rheumatoid factor expression in peripheral blood of patients with rheumatoid arthritis
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摘要 目的:检测类风湿关节炎(RA)患者体内白细胞介素(IL)-23和类风湿因子(RF)的表达,探讨IL-23在RA发病中的作用及其与RF的关系,为RA的早期诊断和进一步阐明RA的发病机制提供理论依据。方法:采用逆转录-聚合酶链反应(RT-PCR)检测66例RA患者和44例健康对照者外周血单个核细胞(PBMC)中IL-23p19 mRNA的表达水平,采用酶联免疫吸附试验(ELISA)检测血清IL-23浓度,采用免疫比浊法检测血清RF的浓度。结果:RT-PCR显示RA患者PBMC中IL-23p19 mRNA的表达[(45.2±11.7)%]显著高于健康对照组[(23.8±9.5)%],ELISA检测结果显示RA患者血清IL-23水平[(114.47±42.70)ng/L]显著高于健康对照组[(70.81±28.85)ng/L],差异均有统计学意义(均P<0.05)。RA患者血清IL-23水平与RF含量无明显相关性(r=0.389,P>0.05)。结论:RA患者体内IL-23在基因和蛋白水平均过表达,提示IL-23可能参与了RA的免疫病理过程,在RA的发病中发挥作用。 Objective: To detect the expression of interleukin(IL)-23 and rheumatoid factor(RF) in rheumatoid arthritis(RA) patients and to explore the role of IL-23 in the pathogenesis of RA and its relationship with the RF,for early diagnosis of RA and further clarify the pathogenesis of RA provides theoretical basis.Methods: IL-23p19 mRNA expression in peripheral blood mononuclear cells(PBMCs) of 66 RA patients and 44 healthy controls was detected by reverse transcription-polymerase chain reaction(RT-PCR),serum IL-23 concentration were measured by enzyme-linked immunosorbent assay(ELISA),serum RF concentrations were measured by immunoturbidimetry.Results: RT-PCR showed IL-23p19 mRNA expression in PBMC of RA patients [(45.2±11.7)%] was significantly higher than that of healthy controls [(23.8±9.5)%],ELISA results showed IL-23 concentration in serum of RA patients [(114.47±42.70) ng/L] was significantly higher than that in healthy controls [(70.81±28.85) ng/L],the differences were significant(P0.05),but IL-23 and RF showed no significant correlation(r=0.389,P0.05).Conclusion: IL-23 in gene and protein levels in RA patients are over-expression,suggesting that IL-23 may be involved in the immune pathogenesis of RA and play the role in the pathogenesis of RA.
作者 张国华 吕智
出处 《中国医药导报》 CAS 2011年第18期23-25,共3页 China Medical Herald
关键词 类风湿关节炎 白细胞介素-23 类风湿因子 Rheumatoid arthritis Interleukin-23 Rheumatoid factor
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