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Immune and hemorheological changes in Chronic Fatigue Syndrome

机译:慢性疲劳综合征的免疫和血液流变学变化

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Background Chronic Fatigue Syndrome (CFS) is a multifactorial disorder that affects various physiological systems including immune and neurological systems. The immune system has been substantially examined in CFS with equivocal results, however, little is known about the role of neutrophils and natural killer (NK) phenotypes in the pathomechanism of this disorder. Additionally the role of erythrocyte rheological characteristics in CFS has not been fully expounded. The objective of this present study was to determine deficiencies in lymphocyte function and erythrocyte rheology in CFS patients. Methods Flow cytometric measurements were performed for neutrophil function, lymphocyte numbers, NK phenotypes (CD56dimCD16+ and CD56brightCD16-) and NK cytotoxic activity. Erythrocyte aggregation, deformability and fibrinogen levels were also assessed. Results CFS patients (n = 10) had significant decreases in neutrophil respiratory burst, NK cytotoxic activity and CD56brightCD16- NK phenotypes in comparison to healthy controls (n = 10). However, hemorheological characteristic, aggregation, deformability, fibrinogen, lymphocyte numbers and CD56dimCD16+ NK cells were similar between the two groups. Conclusion These results indicate immune dysfunction as potential contributors to the mechanism of CFS, as indicated by decreases in neutrophil respiratory burst, NK cell activity and NK phenotypes. Thus, immune cell function and phenotypes may be important diagnostic markers for CFS. The absence of rheological changes may indicate no abnormalities in erythrocytes of CFS patients.
机译:背景慢性疲劳综合症(CFS)是一种多因素疾病,会影响各种生理系统,包括免疫系统和神经系统。在CFS中已经对免疫系统进行了实质性检查,结果尚不清楚,但是,关于中性粒细胞和自然杀伤(NK)表型在该病发病机理中的作用了解甚少。此外,红细胞流变学特性在CFS中的作用尚未得到充分阐明。本研究的目的是确定CFS患者淋巴细胞功能和红细胞流变性的缺陷。方法采用流式细胞术检测中性粒细胞功能,淋巴细胞数量,NK表型(CD56 dim CD16 + 和CD56 bright CD16 -< / sup>)和NK细胞毒性活性。还评估了红细胞聚集,可变形性和纤维蛋白原水平。结果CFS患者(n = 10)与健康对照组(n = 10)相比,中性粒细胞呼吸爆发,NK细胞毒性活性和CD56 CD16 - NK表型显着降低。 。两组的血液流变学特性,聚集性,可变形性,纤维蛋白原,淋巴细胞数量和CD56 dim CD16 + NK细胞相似。结论这些结果表明,免疫功能异常是CFS机制的潜在原因,中性粒细胞呼吸爆发,NK细胞活性和NK表型的降低表明了这一点。因此,免疫细胞功能和表型可能是CFS的重要诊断标志。流变学改变的缺乏可能表明CFS患者的红细胞没有异常。

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