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本文引用的文献

1
Association of IL18 genetic polymorphisms with Chagas disease in Latin American populations.白细胞介素 18 基因多态性与拉丁美洲人群中恰加斯病的关联。
PLoS Negl Trop Dis. 2019 Nov 21;13(11):e0007859. doi: 10.1371/journal.pntd.0007859. eCollection 2019 Nov.
2
Genomic medicine in Chagas disease.克氏锥虫病的基因组医学。
Acta Trop. 2019 Sep;197:105062. doi: 10.1016/j.actatropica.2019.105062. Epub 2019 Jun 12.
3
Disease Tolerance and Pathogen Resistance Genes May Underlie Persistence and Differential Progression to Chagas Disease Cardiomyopathy.疾病耐受和病原体抗性基因可能是导致恰加斯病心肌病持续存在和不同进展的基础。
Front Immunol. 2018 Dec 3;9:2791. doi: 10.3389/fimmu.2018.02791. eCollection 2018.
4
Th-17 cytokines are associated with severity of Trypanosoma cruzi chronic infection in pediatric patients from endemic areas of Mexico.在来自墨西哥流行地区的儿科患者中,Th-17细胞因子与克氏锥虫慢性感染的严重程度相关。
Acta Trop. 2018 Feb;178:134-141. doi: 10.1016/j.actatropica.2017.11.009. Epub 2017 Nov 24.
5
Ebi3 Prevents Induced Myocarditis by Dampening IFN-γ-Driven Inflammation.Ebi3通过抑制IFN-γ驱动的炎症反应预防诱导性心肌炎。
Front Immunol. 2017 Sep 26;8:1213. doi: 10.3389/fimmu.2017.01213. eCollection 2017.
6
Chronic Chagas Heart Disease Management: From Etiology to Cardiomyopathy Treatment.慢性恰加斯心脏病管理:从病因学到心肌病治疗。
J Am Coll Cardiol. 2017 Sep 19;70(12):1510-1524. doi: 10.1016/j.jacc.2017.08.004.
7
Chagas disease cardiomyopathy: immunopathology and genetics.恰加斯病性心肌病:免疫病理学与遗传学
Mediators Inflamm. 2014;2014:683230. doi: 10.1155/2014/683230. Epub 2014 Aug 19.
8
Tissue damage control in disease tolerance.疾病耐受中的组织损伤控制。
Trends Immunol. 2014 Oct;35(10):483-94. doi: 10.1016/j.it.2014.08.001. Epub 2014 Aug 30.
9
Myocardial gene expression of T-bet, GATA-3, Ror-γt, FoxP3, and hallmark cytokines in chronic Chagas disease cardiomyopathy: an essentially unopposed TH1-type response.慢性恰加斯病性心肌病中T-bet、GATA-3、Ror-γt、FoxP3及标志性细胞因子的心肌基因表达:一种基本无对抗的TH1型反应
Mediators Inflamm. 2014;2014:914326. doi: 10.1155/2014/914326. Epub 2014 Jul 24.
10
Plasma cytokine expression is associated with cardiac morbidity in chagas disease.血浆细胞因子表达与恰加斯病的心脏并发症有关。
PLoS One. 2014 Mar 6;9(3):e87082. doi: 10.1371/journal.pone.0087082. eCollection 2014.

影响干扰素-γ产生和 Th1 细胞分化的基因多态性与进展为恰加斯病心肌病相关。

Polymorphisms in Genes Affecting Interferon-γ Production and Th1 T Cell Differentiation Are Associated With Progression to Chagas Disease Cardiomyopathy.

机构信息

Heart Institute (InCor), University of São Paulo School of Medicine (FMUSP), São Paulo, Brazil.

Institute for Investigation in Immunology (iii), INCT, São Paulo, Brazil.

出版信息

Front Immunol. 2020 Jul 7;11:1386. doi: 10.3389/fimmu.2020.01386. eCollection 2020.

DOI:10.3389/fimmu.2020.01386
PMID:32733459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7358543/
Abstract

Chagas disease, caused by the protozoan , is endemic in Latin America. Thirty percent of infected individuals develop chronic Chagas cardiomyopathy (CCC), an inflammatory dilated cardiomyopathy that is the most important clinical consequence of infection, while the others remain asymptomatic (ASY). IFN-γ and IFN-γ-producing Th1-type T cells are increased in peripheral blood and CCC myocardium as compared to ASY patients, while the Th1-antagonizing cytokine IL-10 is more expressed in ASY patients. Importantly IFN-γ-producing Th1-type T cells are the most frequent cytokine-producing T cell subset in CCC myocardium, while expression of Th1-antagonizing cytokines IL-10 and IL-4 is unaltered. The control of IFN-γ production by Th1-type T cells may be a key event for progression toward CCC. A genetic component to disease progression was suggested by the familial aggregation of cases and the association of gene polymorphisms with CCC development. We here investigate the role of gene polymorphisms (SNPs) in several genes involved in the control of IFN-γ production and Th1 T cell differentiation in CCC development. We studied a Brazilian population including 315 CCC cases and 118 ASY subjects. We assessed 35 Tag SNPs designed to represent all the genetic information contained in the , and genes. We found 2 SNPs (rs2546893, rs919766) and a trend of association for a SNP (rs3024496) to be significantly associated with the ASY group. these associations were confirmed by multivariate analysis and allele tests. The rs919766C, 12rs2546893G, and rs3024496C alleles were associated to an increase risk to CCC development. Our data show that novel polymorphisms affecting and , but not or genes play a role in genetic susceptibility to CCC development. This might indicate that the increased Th1 differentiation and IFN-γ production associated with CCC is genetically controlled.

摘要

恰加斯病由原生动物引起,在拉丁美洲流行。30%的感染者会发展为慢性恰加斯心肌病(CCC),这是感染的最重要临床后果,而其余人则无症状(ASY)。与 ASY 患者相比,外周血和 CCC 心肌中的 IFN-γ和 IFN-γ产生 Th1 型 T 细胞增加,而 Th1 拮抗细胞因子 IL-10 在 ASY 患者中表达更多。重要的是,IFN-γ产生 Th1 型 T 细胞是 CCC 心肌中最常见的细胞因子产生 T 细胞亚群,而 Th1 拮抗细胞因子 IL-10 和 IL-4 的表达不变。Th1 型 T 细胞 IFN-γ产生的控制可能是向 CCC 进展的关键事件。病例的家族聚集和基因多态性与 CCC 发展的关联表明疾病进展存在遗传成分。我们在此研究了几个参与 IFN-γ产生和 Th1 T 细胞分化控制的基因中基因多态性(SNP)在 CCC 发展中的作用。我们研究了包括 315 例 CCC 病例和 118 例 ASY 患者在内的巴西人群。我们评估了 35 个 Tag SNP,旨在代表包含在 、和 基因中的所有遗传信息。我们发现 2 个 SNP(rs2546893、rs919766)和一个 SNP(rs3024496)的趋势与 ASY 组显著相关。这些关联通过多变量分析和等位基因测试得到证实。rs919766C、12rs2546893G 和 rs3024496C 等位基因与 CCC 发展的风险增加相关。我们的数据表明,影响 和 但不影响 或 基因的新多态性在 CCC 发展的遗传易感性中起作用。这可能表明与 CCC 相关的 Th1 分化和 IFN-γ产生增加是由遗传控制的。