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无症状慢性恰加斯病患者与健康对照者免疫反应基因的差异表达。

Differential Expression of Immune Response Genes in Asymptomatic Chronic Chagas Disease Patients Healthy Subjects.

机构信息

Instituto de Parasitología y Biomedicina López-Neyra, Consejo Superior de Investigaciones Científicas, Granada, Spain.

Instituto Universitario de Enfermedades Tropicales y Salud Pública de Canarias, Universidad de La Laguna, La Laguna, Spain.

出版信息

Front Cell Infect Microbiol. 2021 Sep 6;11:722984. doi: 10.3389/fcimb.2021.722984. eCollection 2021.

Abstract

Infection by the parasite causes Chagas disease and triggers multiple immune mechanisms in the host to combat the pathogen. Chagas disease has a variable clinical presentation and progression, producing in the chronic phase a fragile balance between the host immune response and parasite replication that keeps patients in a clinically silent asymptomatic stage for years. Since the parasite is intracellular and replicates within cells, the cell-mediated response of the host adaptive immunity plays a critical role. This function is mainly orchestrated by T lymphocytes, which recognize parasite antigens and promote specific functions to control the infection. However, little is known about the immunological markers associated with this asymptomatic stage of the disease. In this large-scale analysis, the differential expression of 106 immune system-related genes has been analyzed using high-throughput qPCR in antigen-stimulated PBMC from chronic Chagas disease patients with indeterminate form (IND) and healthy donors (HD) from endemic and non-endemic areas of Chagas disease. This analysis revealed that there were no differences in the expression level of most genes under study between healthy donors from endemic and non-endemic areas determined by PCA and differential gene expression analysis. Instead, PCA revealed the existence of different expression profiles between IND patients and HD ( < 0.0001), dependent on the 32 genes included in PC1. Differential gene expression analysis also revealed 23 upregulated genes (expression fold change > 2) and 11 downregulated genes (expression fold change < 0.5) in IND patients HD. Enrichment analysis showed that several upregulated genes in IND patients participate in relevant immunological pathways such as antigen-dependent B cell activation, stress induction of HSP regulation, NO2-dependent IL12 pathway in NK cells, and cytokine-inflammatory response. The antigen-specific differential gene expression profile detected in these patients and the relevant immunological pathways that seem to be activated could represent potential biomarkers of the asymptomatic form of Chagas disease, helpful to diagnosis and infection control.

摘要

寄生虫感染会导致恰加斯病,并触发宿主的多种免疫机制来对抗病原体。恰加斯病的临床表现和进展具有多变性,在慢性期,宿主免疫反应和寄生虫复制之间会产生脆弱的平衡,使患者多年处于临床无症状的无症状期。由于寄生虫是细胞内的,并在细胞内复制,宿主适应性免疫的细胞介导反应发挥着关键作用。这种功能主要由 T 淋巴细胞协调,它们识别寄生虫抗原并促进特定功能以控制感染。然而,对于这种疾病无症状期相关的免疫标志物知之甚少。在这项大规模分析中,使用高通量 qPCR 分析了来自慢性恰加斯病不确定型(IND)患者和来自恰加斯病流行和非流行地区的健康供体(HD)的抗原刺激 PBMC 中 106 种与免疫系统相关的基因的差异表达。这项分析表明,通过 PCA 和差异基因表达分析,来自流行和非流行地区的健康供体中大多数研究基因的表达水平没有差异。相反,PCA 显示了 IND 患者和 HD 之间存在不同的表达谱(<0.0001),这取决于 PC1 中包含的 32 个基因。差异基因表达分析还显示,IND 患者与 HD 相比,有 23 个上调基因(表达倍数变化>2)和 11 个下调基因(表达倍数变化<0.5)。富集分析表明,IND 患者中几个上调的基因参与了相关的免疫途径,如抗原依赖性 B 细胞激活、应激诱导的 HSP 调节、NK 细胞中 NO2 依赖性 IL12 途径和细胞因子炎症反应。这些患者中检测到的抗原特异性差异基因表达谱和似乎被激活的相关免疫途径可能代表了恰加斯病无症状形式的潜在生物标志物,有助于诊断和感染控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d08/8450343/f142e0bc7f83/fcimb-11-722984-g001.jpg

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