首页> 美国卫生研究院文献>Case Reports in Medicine >Serum Cytokine Profile in a Patient Diagnosed with Dysferlinopathy
【2h】

Serum Cytokine Profile in a Patient Diagnosed with Dysferlinopathy

机译:诊断为铁蛋白异常的患者的血清细胞因子谱

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。
获取外文期刊封面目录资料

摘要

Limb-girdle muscular dystrophy type 2 (LGMD2B) is a mild form of dysferlinopathy, characterized by limb weakness and wasting. It is an autosomal recessive disease, with currently 140 mutations in the LGMD2B gene identified. Lack of functional dysferlin inhibits muscle fiber regeneration in voluntary muscles, the main pathological finding in LGMD2B patients. However, the immune system has been suggested to contribute to muscle cell death and tissue regeneration. Serum levels of 27 cytokines were evaluated in a dysferlinopathy patient. Levels of 8 cytokines differed in patient serum compared to controls. Five cytokines (IL-10, IL-17, CCL2, CXCL10, and G-CSF) were higher while 3 were lower in the patient than in controls (IL-2, IL-8, and CCL11). Together, these data on serum cytokine profile of this dysferlinopathy patient suggest immune response activation, which could explain leukocyte infiltration in the muscle tissue.
机译:2型肢带型肌营养不良症(LGMD2B)是一种轻度形式的营养不良症,特征是四肢无力和消瘦。它是一种常染色体隐性遗传疾病,目前在LGMD2B基因中鉴定出140个突变。功能性dysferlin的缺乏会抑制自愿性肌肉中的肌肉纤维再生,这是LGMD2B患者的主要病理发现。然而,已经提出免疫系统有助于肌肉细胞死亡和组织再生。在一个铁蛋白缺乏症患者中评估了27种细胞因子的血清水平。与对照相比,患者血清中8种细胞因子的水平有所不同。患者中五种细胞因子(IL-10,IL-17,CCL2,CXCL10和G-CSF)比对照组(IL-2,IL-8和CCL11)高,而三种细胞因子低。总的来说,这些关于该铁蛋白障碍病患者血清细胞因子谱的数据表明免疫应答被激活,这可以解释白细胞在肌肉组织中的浸润。

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