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免疫性血小板减少症患者白细胞介素-35水平降低。

Decreased IL-35 levels in patients with immune thrombocytopenia.

作者信息

Yang Yanhui, Xuan Min, Zhang Xian, Zhang Donglei, Fu Rongfeng, Zhou Fangfang, Ma Li, Li Huiyuan, Xue Feng, Zhang Lei, Yang Renchi

机构信息

Institute of Hematology and Hospital of Blood Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College, 288 Nanjing Road, Tianjin 300020, China; 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Key Laboratory of Hormones and Development (Ministry of Health), Metabolic Diseases Hospital & Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin 300070, China.

Institute of Hematology and Hospital of Blood Diseases, Chinese Academy of Medical Sciences & Peking Union Medical College, 288 Nanjing Road, Tianjin 300020, China.

出版信息

Hum Immunol. 2014 Aug;75(8):909-13. doi: 10.1016/j.humimm.2014.06.019. Epub 2014 Jun 30.

Abstract

IL-35 is a novel heterodimeric anti-inflammatory cytokine consisting of Epstein-Barr virus-induced gene 3 (EBI3) and the p35 subunit of IL-12. IL-35 has been shown to possess the potency of inhibiting the CD4+ effector T cells and alleviating autoimmune diseases. In the study we investigated the levels of IL-35 as well as its prospective role in immune thrombocytopenia (ITP).ELISA was adopted to measure plasma IL-35, TGF-β and IL-10 levels. The mRNA expression levels of P35 and EBI3 in peripheral blood mononuclear cells (PBMCs) were studied based on real-time quantitative PCR. The correlation between plasma cytokine levels and clinical parameters was analyzed. Significantly lower plasma IL-35 levels were found in active ITP patients compared with those in remission (p = 0.017) and the healthy controls (p < 0.001). In active ITP patients, the plasma IL-35 levels displayed a significantly positive correlation with platelet counts (r = 0.5335, p < 0.0008). Further, P35 mRNA expression levels were lower in patients with active ITP than patients in remission (p = 0.033) and normal controls (p = 0.016).Thus, for the first time, this research reported a dramatically decreased IL-35 levels in ITP patients, suggesting that IL-35 may be involved in the pathogenesis of ITP.

摘要

白细胞介素-35(IL-35)是一种新型的异二聚体抗炎细胞因子,由EB病毒诱导基因3(EBI3)和白细胞介素-12的p35亚基组成。研究表明,IL-35具有抑制CD4 +效应T细胞和缓解自身免疫性疾病的能力。在本研究中,我们调查了IL-35的水平及其在免疫性血小板减少症(ITP)中的潜在作用。采用酶联免疫吸附测定法(ELISA)测量血浆中IL-35、转化生长因子-β(TGF-β)和白细胞介素-10(IL-10)的水平。基于实时定量聚合酶链反应(PCR)研究外周血单个核细胞(PBMC)中P35和EBI3的信使核糖核酸(mRNA)表达水平。分析血浆细胞因子水平与临床参数之间的相关性。与缓解期患者(p = 0.017)和健康对照组(p < 0.001)相比,活动期ITP患者血浆IL-35水平显著降低。在活动期ITP患者中,血浆IL-35水平与血小板计数呈显著正相关(r = 0.5335,p < 0.0008)。此外,活动期ITP患者的P35 mRNA表达水平低于缓解期患者(p = 0.033)和正常对照组(p = 0.016)。因此,本研究首次报道ITP患者IL-35水平显著降低,提示IL-35可能参与ITP的发病机制。

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