首页> 美国卫生研究院文献>Hippokratia >CD4+/CD25+ T-Lymphocytes and Th1/Th2 regulation in dilated cardiomyopathy
【2h】

CD4+/CD25+ T-Lymphocytes and Th1/Th2 regulation in dilated cardiomyopathy

机译:CD4 + / CD25 + T淋巴细胞和Th1 / Th2调节在扩张型心肌病中的作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>Objective: Autoimmune mechanisms are often involved in the pathogenesis of Dilated Cardiomyopathy (DCM) and Th1 immune response against cardiac antigens plays a pivotal role in disease development.>Methods: IL-2 receptor (CD4+/CD25+) and cytokines IL-2, IFN-γ, IL-10 were studied in 42 patients (17 with DCM - DCM group, 10 patients with hypertrophic cardiac disease - HCD group, and 15 healthy volunteers - Control group). DCM group was subdivided in: DCM-1 (9 patients with recent disease onset) and DCM-2 (8 patients with chronic DCM). The % CD4+/CD25+ T-lymphocytes were analyzed by double fluorescence flow cytometry both ex vivo and after phytohaemagglutinin (PHA)-cultures with/without 5 and 10 microgr of human cardiac myosin. The cytokines were measured using Enzyme-Linked Immunosorbant Assay (ELISA) method.>Results: Ex vivo analysis: In DCM group, CD4+/CD25+ T-cells significantly increased compared to other groups (p<0.05), due exclusively to DCM-2 subgroup (p=0.019). In PHA cultures in DCM-2 subgroup CD4+/CD25+ T-lymphocytes were significantly increased compared to all other groups (p<0.001). The addition of myosin in the cultures of DCM-2 subgroup maintained the same result. >In cultures supernatants in DCM-2 subgroup, IL-2 levels were impressively increased compared to DCM-1 subgroup (p=5.91x10-6), HCD and Control groups (p<0.001). Addition of antigen decreased significantly IL-2 levels in DCM-2 subgroup (p=0.01). IFN-γ levels followed the same pattern of alterations. IL-10 levels were significantly increased in both DCM subgroups compared to HCD and Control groups (p<0.05).>Conclusions: Increased peripheral CD4+/CD25+ T-cells found in chronic DCM could be a useful prognostic marker in DCM progress. Increased synthesis of IL-2 and IFN-γ and varying IL-10 levels reflects a Th1 pattern of immune response during chronic disease and implies active cellular immunity process, related to poor prognosis. Thus, analysis of the Th1/Th2 phenotype may be useful in disease monitoring in patients with DCM.This paper is a part of PhD thesis. It has been published at the abstract book of the Acute Cardiac Care congress 2010.
机译:>目的:自身免疫机制经常参与扩张型心肌病(DCM)的发病机制,并且针对心脏抗原的Th1免疫应答在疾病发展中起着关键作用。>方法:在42例患者中研究了CD4 + / CD25 +受体(CD4 + / CD25 +)和细胞因子IL-2,IFN-γ,IL-10(其中DCM-DCM组17例,肥厚性心脏病10例-HCD组,15名健康志愿者-对照组) 。 DCM组细分为:DCM-1(9例近期发病的患者)和DCM-2(8例慢性DCM的患者)。通过双荧光流式细胞术在离体和有/无5和10 microgr人心肌肌球蛋白的植物血凝素(PHA)培养后,通过双荧光流式细胞术分析%CD4 + / CD25 + T淋巴细胞。 >结果:离体分析:在DCM组中,CD4 + / CD25 + T细胞比其他组显着增加(p <0.05),完全归因于DCM-2子组(p = 0.019)。与所有其他组相比,在DCM-2亚组的PHA培养物中,CD4 + / CD25 + T淋巴细胞显着增加(p <0.001)。在DCM-2亚组的培养物中添加肌球蛋白保持了相同的结果。 >在DCM-2亚组的培养上清液中,与DCM-1亚组(p = 5.91x10-6),HCD和对照组(p <0.001)相比,IL-2水平显着增加。在DCM-2亚组中,抗原的添加显着降低了IL-2水平(p = 0.01)。 IFN-γ水平遵循相同的变化模式。与HCD组和对照组相比,两个DCM亚组中的IL-10水平均显着升高(p <0.05)。>结论:在慢性DCM中发现的外周CD4 + / CD25 + T细胞增加可能是有用的预后指标在DCM进度中。 IL-2和IFN-γ的合成增加以及IL-10水平的变化反映了慢性疾病期间Th1免疫应答的模式,并暗示了活跃的细胞免疫过程,与预后不良有关。因此,对Th1 / Th2表型的分析可能对DCM患者的疾病监测有用。本文是博士学位论文的一部分。它已发表在2010年急性心脏护理大会的摘要中。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号