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首页> 外文期刊>Japanese journal of infectious diseases >Association of IL10, IL4, IFNG, and CTLA4 Gene Polymorphisms with Efavirenz Hypersensitivity Reaction in Patients Infected with Human Immunodeficiency Virus
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Association of IL10, IL4, IFNG, and CTLA4 Gene Polymorphisms with Efavirenz Hypersensitivity Reaction in Patients Infected with Human Immunodeficiency Virus

机译:IL10,IL4,IFNG和CTLA4基因多态性与感染人类免疫缺陷病毒的依夫韦伦超敏反应的相关性

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We evaluated interleukin-10 (IL10) -592 C/A, IL4-589 C/T, interferon gamma (IFNG)+874 A/T, cytotoxic T-lymphocyte-associated antigen 4 (CTLA4)+49 A/G gene polymorphisms associated with efavirenz hypersensitivity reaction. A total of 63 human immunodeficiency virus-positive patients under treatment at a public hospital were included in the study, of whom 21 presented with efavirenz hypersensitivity. Patients who presented with efavirenz hypersensitivity reaction showed a higher frequency of the IL10 -592A allele than the controls (p=0.028). The allele A was associated with increased risk of efavirenz hypersensitivity (odds ratio=2.40). In case of IL4, a significant difference in the frequency of the IL4 -589 (C/T) polymorphism was not observed between patients and controls. A significant inverse correlation was observed when comparing the CTLA4+49A/G and IL4 -589 C/T polymorphisms (r=-0.650, p=0.001); that is, the CTLA4 +49GG genotype, involved with the lowest capacity of inhibition, was inversely correlated IL4-589TT genotype, which induces high production of IL-4. With respect to the CTLA4+49A/G and IFNG+874T/A gene polymorphisms, significant differences in allele and genotype frequencies were not observed between the groups. Therefore, our data suggest that polymorphisms in regulatory regions of cytokine genes could modulate an individual’s susceptibility to efavirenz hypersensitivity reaction.
机译:我们评估了白介素10(IL10)-592 C / A,IL4-589 C / T,干扰素γ(IFNG)+874 A / T,细胞毒性T淋巴细胞相关抗原4(CTLA4)+49 A / G基因多态性与依非韦伦超敏反应。该研究总共包括了63名在公立医院接受治疗的人类免疫缺陷病毒阳性患者,其中21名表现出依非韦伦超敏反应。出现依非韦伦超敏反应的患者显示IL10 -592A等位基因的频率高于对照组(p = 0.028)。等位基因A与依非韦伦超敏反应的风险增加相关(比值= 2.40)。在IL4的情况下,患者和对照组之间未观察到IL4 -589(C / T)多态性频率的显着差异。比较CTLA4 + 49A / G和IL4 -589 C / T多态性时,存在显着的负相关(r = -0.650,p = 0.001)。即抑制作用最低的CTLA4 + 49GG基因型与IL4-589TT基因型呈负相关,从而诱导IL-4的大量产生。关于CTLA4 + 49A / G和IFNG + 874T / A基因多态性,两组之间在等位基因和基因型频率上没有显着差异。因此,我们的数据表明,细胞因子基因调控区的多态性可能会调节个体对依非韦伦超敏反应的敏感性。

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