ПОЛИМОРФИЗМ ГЕНОВ ИММУНОСУПРЕССОРНЫХ ЦИТОКИНОВ IL-10 И TGF-β ПРИ ТУБЕРКУЛЕЗНОЙ ИНФЕКЦИИ

IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL
Ye. G. Churina, O. I. Urazova, V. V. Novitsky, O. V. Filinyuk
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引用次数: 0

Abstract

The aim of the work was the study of connection of allelic polymorphism of  IL10  and  TGF В genes with changes in the basal and BCG-induced production of immunosuppressive cytokines IL-10 and TGF-β by mononuclear leukocytes  in vitro  in patients with the first diagnosed pulmonary tuberculosis (TB), depending on the clinical form of the disease. The evaluation of the cytokines production was conducted by measuring its concentration in culture supernatants by ELISA. The allele-specific amplification of specific stretches of the genome was used for the study of polymorphic genes of cytokines. The DNA and supernatants of culture suspensions of blood mononuclear leucocytes in healthy volunteers and patients with TB were the material of the research. It was shown in the research conducted that the basal and BCG-induced over-production of IL-10  in vitro  occurs in patients with TB, regardless of the genotype of the locus of  C-592AIL10  gene. In addition, genotype  AA  of polymorphism of  IL10 gene in patients with infiltrative and disseminated TB is associated with the maximum production of IL-10  in vitro and genotype  CC  – with the minimum production of this cytokine  in vitro . Analysis of the production of TGF-β  in vitro  in patients with TB showed its increase only in case of carriage of allele  T  ( C-509T ) of  TGFB  gene. In patients with disseminated TB and homosygotic genotype  TT  the increase in both basal and BCG-induced production of TGF-β was determined, and in patients with infiltrative TB – only after induction of cells by BCG-antigen. Thus, the over-production of cytokines with inhibiting activity in patients with TB is genetically determined and promotes the formation of suppressive mode of immune-regulation. The increase in the secretion of cytokines IL-10 and TGF-β  in vitro  in patients with TB are associated with carriage of allele  A  and genotype  AA ( C-592A ) of  IL10 gene and allele  T  and genotype  TT  ( C-509T ) of  TGFB  gene.
肺结核感染中免疫抑制细胞因子IL-10和TGFβ基因的多态性
这项工作的目的是研究IL-10和TGF- В基因等位基因多态性与首次诊断为肺结核(TB)的患者体外单核白细胞基础和bcg诱导的免疫抑制细胞因子IL-10和TGF-β产生的变化之间的联系,这取决于疾病的临床形式。通过ELISA法测定细胞因子在培养上清液中的浓度来评价细胞因子的产生。基因组特异片段的等位基因特异性扩增用于细胞因子多态性基因的研究。以健康志愿者和结核患者血单核白细胞培养悬液的DNA和上清液为研究材料。本研究表明,无论C-592AIL10基因位点的基因型如何,结核患者体外均存在基底和bcg诱导的IL-10过量产生。此外,浸润性和播散性结核患者IL-10基因多态性基因型AA与体外IL-10产量最高相关,基因型CC -与体外IL-10产量最低相关。对TB患者体外TGF-β产生的分析显示,只有携带TGFB基因的等位基因T (C-509T)时,TGF-β的产生才会增加。在弥散性结核和纯合子基因型TT患者中,测定了基础和bcg诱导的TGF-β产量的增加,而在浸润性结核患者中,仅通过bcg抗原诱导细胞后,测定了TGF-β产量的增加。因此,结核患者体内具有抑制活性的细胞因子的过量产生是由遗传决定的,并促进了免疫调节抑制模式的形成。TB患者体外细胞因子IL-10和TGF-β分泌增加与IL10基因等位基因A和基因型AA (C-592A)以及TGFB基因等位基因T和基因型TT (C-509T)的携带有关。
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来源期刊
Byulleten Sibirskoy Meditsiny
Byulleten Sibirskoy Meditsiny MEDICINE, GENERAL & INTERNAL-
CiteScore
0.70
自引率
50.00%
发文量
102
审稿时长
8 weeks
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