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首页> 外文期刊>Archives of virology >Role of coxsackievirus and adenovirus receptor (CAR) expression and viral load of adenovirus and enterovirus in patients with dilated cardiomyopathy
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Role of coxsackievirus and adenovirus receptor (CAR) expression and viral load of adenovirus and enterovirus in patients with dilated cardiomyopathy

机译:柯萨奇病毒和腺病毒受体(CAR)表达以及腺病毒和肠病毒的病毒载量在扩张型心肌病患者中的作用

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摘要

Enteroviruses (EVs) and adenoviruses (AdVs) are two important etiological agents of viral myocarditis and dilated cardiomyopathy (DCM). Both these viruses share a common receptor, the coxsackievirus and adenovirus receptor (CAR), for their infection. However, the role of viral load and CAR expression in disease severity has not yet been completely elucidated. The present study aimed to determine viral load of EV and AdV in DCM patients and correlate them with the level of CAR expression in these patients. Sixty-three DCM cases and 30 controls, each of whom died of heart disease other than DCM and non-cardiac disease respectively, were included. Viral load was determined by TaqMan real-time PCR using primers and probes specific for the AdV hexon gene and the 5'UTR region of EV. The CAR mRNA level was semi-quantitated by RT-PCR, and antigen expression was studied by immunohistochemistry. A significantly high AdV load (p < 0.05) and CAR expression (p < 0.05) were observed in DCM cases versus controls, whereas the EV load showed no significant difference. The data suggests a clinical threshold of 128 AdV copies/500 ng of DNA for DCM, with 66.7 % sensitivity and 65 % specificity. A positive correlation between AdV load and CAR expression (p < 0.001) was also observed in DCM cases. The high adenoviral load and increased CAR expression in DCM and their association with adverse disease outcome indicates role of both virus and receptor in disease pathogenesis. Thus, the need for targeting both the virus and the receptor for treatment of viral myocarditis and early DCM requires further confirmation with larger studies.
机译:肠病毒(EVs)和腺病毒(AdVs)是病毒性心肌炎和扩张型心肌病(DCM)的两种重要病因。这两种病毒共享一个共同的受体,即柯萨奇病毒和腺病毒受体(CAR)进行感染。然而,尚未完全阐明病毒载量和CAR表达在疾病严重程度中的作用。本研究旨在确定DCM患者的EV和AdV病毒载量,并将其与这些患者的CAR表达水平相关。包括63例DCM病例和30例对照,每例分别死于DCM和非心脏病以外的心脏病。通过TaqMan实时PCR使用对AdV六邻体基因和EV的5'UTR区具有特异性的引物和探针确定病毒载量。通过RT-PCR半定量CAR mRNA水平,并通过免疫组织化学研究抗原表达。与对照组相比,在DCM病例中观察到AdV负荷显着较高(p <0.05)和CAR表达(p <0.05),而EV负荷无明显差异。数据表明,DCM的临床阈值为128 AdV拷贝/ 500 ng DNA,敏感性为66.7%,特异性为65%。在DCM病例中,还观察到AdV负荷与CAR表达之间呈正相关(p <0.001)。 DCM中高腺病毒载量和CAR表达增加以及它们与不良疾病后果的关系表明病毒和受体在疾病发病机理中的作用。因此,需要同时针对病毒和受体同时治疗病毒性心肌炎和早期DCM,这需要更大规模的研究进一步证实。

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