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Single nucleotide polymorphisms in immune system genes and their association with clinical symptoms persistence in dengue-infected persons

机译:登革热感染者免疫系统基因的单核苷酸多态性及其与临床症状持续性的关系

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This study was undertaken to determine the prevalence of dengue clinical symptom persistence during 60 days of disease follow up, in patients of Espirito Santo state (ES)-Brazil and to evaluate the relation of single nucleotide polymorphisms (SNPs) in Fc gamma RIIa, CD209, VDR, TNF-alpha, IL-4, IL-6 and IFN-gamma genes with symptom persistence. During 2012-2013, 96 blood samples from individuals diagnosed with symptomatic dengue were collected. Clinical symptom persistence in 60 days of follow-up was assessed by a clinical and epidemiological questionnaire filled in 4 interviews. SNP genotyping was performed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). In two months of monitoring the dengue infection, we observed that symptoms persisted in 38.5% (37/96) of dengue patients at the end of the first month (D30) and in 11.5% (11/96) of dengue patients at the end of the second month (D60). Our results show an association between Fc gamma RIIa, TNF-alpha, and IL-6 gene SNPs and symptom persistence and an association trend with CD209, IL-4 and IFN-gamma gene SNPs. Our findings may increase the knowledge on the pathophysiological mechanisms of persistent symptoms of infection with the dengue virus (DENV) and thus help the clinical management of patients. (C) 2015 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
机译:这项研究的目的是确定巴西埃斯皮里图州(ES)-巴西精神病患者在疾病随访60天内的登革热临床症状持续性流行情况,并评估FcγRIIa,CD209中单核苷酸多态性(SNP)的关系。 ,VDR,TNF-α,IL-4,IL-6和IFN-γ基因具有症状持续性。在2012-2013年期间,从确诊为有症状登革热的个体中采集了96份血液样本。通过填写4次访谈的临床和流行病学调查表评估了60天随访中的临床症状持续性。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)进行SNP基因分型。在监测登革热感染的两个月中,我们观察到症状在第一个月月底(D30)持续存在于38.5%(37/96)的登革热患者中,并在月末持续存在于11.5%(11/96)的登革热患者中第二个月(D60)的日期。我们的结果显示FcγRIIa,TNF-α和IL-6基因SNP之间的关联和症状持续性以及与CD209,IL-4和IFN-γ基因SNP的关联趋势。我们的发现可能会增加对登革热病毒(DENV)持续感染症状的病理生理机制的了解,从而有助于患者的临床管理。 (C)2015年美国组织相容性与免疫遗传学学会。由Elsevier Inc.出版。保留所有权利。

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