基因变异TNFA (rs361525)与发生登革热症状的易感性增加有关

IF 1.5 4区 医学 Q4 IMMUNOLOGY
Mónica Edith Villanueva-Aguilar, Lourdes Del Carmen Rizo-de-la-Torre, María Del Pilar Granados-Muñiz, Andrea Montoya-Fuentes, Héctor Montoya-Fuentes
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引用次数: 0

摘要

登革病毒(DENV)是登革热的致病因子。登革热的症状和体征各不相同,从发热性疾病到出血性综合征。IFITM3和TNFA是先天免疫系统的基因。变异IFITM3 (rs12252t >C)和TNFA (rs1800629 G>A和rs361525 G>A)可能改变基因表达并改变疾病的进程。我们的第一个目标是确定这些变异是否与登革热的易感性和严重程度有关。第二个是评估这些变异与每种症状的关系。我们研究了272例疑似登革热感染病例,其中确诊登革热(DENV+)病例102例,未感染登革热(DENV-)的登革热样病例170例。从墨西哥普通人群中抽取201人作为参考。采用聚合酶链反应-限制性片段长度多态性技术进行基因分型。比值比和置信区间使用皮尔逊卡方检验计算,然后使用二元逻辑回归模型对年龄和性别进行调整。必要时采用霍尔丹校正。我们发现,与一般人群相比,DENV+和DENV-组中TNFA rs361525的a等位基因频率明显更高。在DENV+和DENV-组中,TNFA rs361525的A等位基因频率在DENV+组中较高。广泛的症状与两种TNFA变体的A等位基因有关。我们的结论是,TNFA rs361525增加了对有症状的登革热的易感性,但也可能与其他未知原因的登革热样症状的易感性相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Genetic Variant TNFA (rs361525) Is Associated with Increased Susceptibility to Developing Dengue Symptoms.

Dengue virus (DENV) is the causal agent of dengue fever. The symptoms and signs of dengue vary from febrile illness to hemorrhagic syndrome. IFITM3 and TNFA are genes of the innate immune system. Variants IFITM3 (rs12252 T>C) and TNFA (rs1800629 G > A and rs361525 G>A) might alter gene expression and change the course of the disease. Our first objective was to determine whether these variants were associated with the susceptibility and severity of dengue. The second was to assess the association of these variants with each symptom. We studied 272 cases with suspected dengue infection, of which 102 were confirmed dengue cases (DENV+) and 170 were dengue-like cases without DENV infection (DENV-). Samples of 201 individuals from the general population of Mexico were included as a reference. Genotyping was performed by the polymerase chain reaction-restriction fragment length polymorphism technique. Odds ratios and confidence intervals were calculated using Pearson's chi-square test and later adjusted for age and sex with a binary logistic regression model. Haldane correction is applied when necessary. We found a significantly higher frequency of the A allele of TNFA rs361525 in both the DENV+ and DENV- groups compared with the general population. Focusing on DENV+ and DENV-, the frequency of the A allele of TNFA rs361525 was higher in the DENV+ group. A broad spectrum of symptoms was related to the A allele of both TNFA variants. We conclude that TNFA rs361525 increases the susceptibility to symptomatic dengue but can also be associated with susceptibility to other dengue-like symptoms from unknown causes.

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来源期刊
Viral immunology
Viral immunology 医学-病毒学
CiteScore
3.60
自引率
0.00%
发文量
84
审稿时长
6-12 weeks
期刊介绍: Viral Immunology delivers cutting-edge peer-reviewed research on rare, emerging, and under-studied viruses, with special focus on analyzing mutual relationships between external viruses and internal immunity. Original research, reviews, and commentaries on relevant viruses are presented in clinical, translational, and basic science articles for researchers in multiple disciplines. Viral Immunology coverage includes: Human and animal viral immunology Research and development of viral vaccines, including field trials Immunological characterization of viral components Virus-based immunological diseases, including autoimmune syndromes Pathogenic mechanisms Viral diagnostics Tumor and cancer immunology with virus as the primary factor Viral immunology methods.
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