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首页> 外文期刊>Clinical & developmental immunology. >Analysis of Serum Cytokines and Single-Nucleotide Polymorphisms of SOD1, SOD2, and CAT in Erysipelas Patients
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Analysis of Serum Cytokines and Single-Nucleotide Polymorphisms of SOD1, SOD2, and CAT in Erysipelas Patients

机译:丹毒患者血清细胞因子和SOD1,SOD2和CAT的单核苷酸多态性分析

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摘要

Increased free radical production had been documented in group A ( β -hemolytic) streptococcus infection cases. Comparing 71 erysipelas patients to 55 age-matched healthy individuals, we sought for CAT, SOD1, and SOD2 single polymorphism mutation (SNPs) interactions with erysipelas' predisposition and serum cytokine levels in the acute and recovery phases of erysipelas infection. Whereas female patients had a higher predisposition to erysipelas, male patients were prone to having a facial localization of the infection. The presence of SOD1 G7958, SOD2 T2734, and CAT C262 alleles was linked to erysipelas' predisposition. T and C alleles of SOD2 T2734C individually were linked to patients with bullous and erythematous erysipelas, respectively. G and A alleles of SOD1 G7958A individually were associated with lower limbs and higher body part localizations of the infection, respectively. Serum levels of IL-1 β , CCL11, IL-2R α , CXCL9, TRAIL, PDGF-BB, and CCL4 were associated with symptoms accompanying the infection, while IL-6, IL-9, IL-10, IL-13, IL-15, IL-17, G-CSF, and VEGF were associated with predisposition and recurrence of erysipelas. While variations of IL-1 β , IL-7, IL-8, IL-17, CCL5, and HGF were associated with the SOD2 T2734C SNP, variations of PDFG-BB and CCL2 were associated with the CAT C262T SNP.
机译:在A组(β-溶血性)链球菌感染病例中已证明自由基产生增加。将71例丹毒患者与55个年龄相匹配的健康个体进行比较,我们寻求CAT,SOD1和SOD2单多态性突变(SNP)与丹毒易感性和丹毒感染急性期和恢复期中血清细胞因子水平的相互作用。女性患者容易患丹毒,而男性患者则容易出现面部感染。 SOD1 G7958,SOD2 T2734和CAT C262等位基因的存在与丹毒的易感性有关。 SOD2 T2734C的T和C等位基因分别与患有大疱性丹毒和红斑丹毒的患者相关。 SOD1 G7958A的G和A等位基因分别与感染的下肢和较高的身体部位相关。血清IL-1β,CCL11,IL-2Rα,CXCL9,TRAIL,PDGF-BB和CCL4的水平与感染相关的症状有关,而IL-6,IL-9,IL-10,IL-13, IL-15,IL-17,G-CSF和VEGF与丹毒的易感性和复发有关。尽管IL-1β,IL-7,IL-8,IL-17,CCL5和HGF的变异与SOD2 T2734C SNP有关,但PDFG-BB和CCL2的变异与CAT C262T SNP有关。

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