[白介素-1家族基因多态性与肺炎发病的关系]。

E A Baygozina, V T Dolgih, V I Sovalkin
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引用次数: 0

摘要

尽管对医院性肺炎的研究很多,但目前尚无明确的诊断标准,对医院性肺炎的预后预测主要基于个体临床、仪器、实验室等参数,这些参数在单一发病机制中并不相互关联。外界因素对肺炎的发生发展和决定其预后的影响,得到了充分的重视,而问题在于没有综合的临床和病理生理学方法来评估医院性肺炎的预后,并考虑其免疫遗传学特征。学习的一个方面是免疫系统的医院性肺炎评估,特别是具有诊断和预后价值的细胞因子。众所周知,机体的免疫反应性水平在遗传上是固定的,因此,决定了细胞因子表达编码基因多态性在细胞间相互作用中作为关键参与者的重要性。在本文中,我们发现医院性肺炎的免疫发病因素之一是IL-1β (-511) C- >T和IL-1RN基因多态性。其发生风险的遗传标记是IL-1β (-511) C->T基因等位基因C的携带者。肺炎的严重程度和临床特征与患者IL-1β (-511) C- >T基因等位基因的存在相关。这种多态性的致病作用是由于细胞因子IL-1β的过量产生而产生的。暴露于与具有极性生物学效应的同名细胞因子IL-1RN * 4-IL-1β (-511) C- >T基因单倍型相关的医院性肺炎
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Polymorphism of genes of interleukin-1 family as factor of pathogenesis of nozokomialny pneumonia].

Despite the abundance of research devoted to nosocomial pneumonia, so far there are no clear diagnostic criteria for it and predict the outcome of nosocomial pneumonia is based on the individual clinical, instrumental, laboratory and other parameters that are not related to each other as links in a single pathogenesis. External factors contributing to the development of the pneumonia and determine its prognosis, adequately lit, and the problem lies in the fact that no comprehensive clinical and pathophysiological approach to assessing the outcome of nosocomial pneumonia considering its immunogenetic features. One aspect of learning is nosocomial pneumonia appraisal of immune system, in particular, -- cytokines that have both diagnostic and prognostic value. As is known, the level of immune reactivity of the organism is fixed genetically, therefore, determines the importance polymorphisms of genes coding for the expression of cytokines as key participants in the intercellular interactions. In the present article we found that one of the factors immunopathogenesis of nosocomial pneumonia is a gene polymorphism IL-1β (-511) C-->T and IL-1RN. Genetic markers of risk of its development is the carrier of the allele C of gene IL-1β (-511) C->T. The severity and clinical features of the pneumonia associated with the presence of the genotype of the patients T allele of the gene IL-1β (-511) C-->T. Implementation of the pathogenetic action of this polymorphism is carried out due to overproduction of the cytokine IL-1β. Exposure to nosocomial pneumonia associated with haplotypes IL-1RN * 4-IL-1β (-511) C-->T gene of the same name cytokines having polar biological effects.

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