Instituto de Parasitología y Biomedicina López-Neyra, CSIC, Granada, Spain.
Instituto Universitario de Enfermedades Tropicales y Salud Pública de Canarias, Universidad de La Laguna, La Laguna, Spain.
PLoS Negl Trop Dis. 2023 Jul 13;17(7):e0011474. doi: 10.1371/journal.pntd.0011474. eCollection 2023 Jul.
Patients with chronic Chagas disease present marked clinical and immunological heterogeneity. During the disease, multiple immune mechanisms are activated to fight the parasite. The purpose of this study was to investigate the expression patterns of genes involved in relevant immunological processes throughout the disease in patients with chronic Chagas disease.
METHODOLOGY/PRINCIPAL FINDINGS: High-throughput RT-qPCR with QuantStudio 12K Flex real-time PCR system was used to evaluate the expression of 106 immune-related genes in PBMC from a cohort of cardiac Chagas disease patients (CCC I), asymptomatic patients (IND) and healthy donors (HD) after being stimulated with T. cruzi soluble antigens. Principal component analysis (PCA), cluster analysis and volcano plots were used to identify differentially expressed genes. In addition, gene set enrichment analysis (GSEA) was employed to identify the enriched immunological pathways in which these genes are involved. PCA revealed the existence of a statistically divergent expression profile of the 36 genes correlated with PC1 between CCC I patients and HD (p < 0.0001). Differential gene expression analysis revealed upregulation of 41 genes (expression fold-change > 1.5) and downregulation of 14 genes (expression fold-change < 0.66) (p = 8.4x10-13 to p = 0.007) in CCC I patients versus HD. Furthermore, significant differences in the expression level of specific genes have been identified between CCC I and IND patients (8 up and 1 downregulated). GSEA showed that several upregulated genes in CCC I patients participate in immunological pathways such as antigen-dependent B cell activation, stress induction of HSP regulation, NO2-dependent IL12 pathway in NK cells, cytokines-inflammatory response and IL-10 anti-inflammatory signaling.
Cardiac Chagas disease patients show an antigen-specific differential gene expression profile in which several relevant immunological pathways seem to be activated. Assessment of gene expression profiles reveal unique insights into the immune response that occurs along chronic Chagas disease.
慢性恰加斯病患者表现出明显的临床和免疫异质性。在疾病过程中,多种免疫机制被激活以对抗寄生虫。本研究的目的是研究慢性恰加斯病患者在整个病程中与相关免疫过程相关的基因表达模式。
方法/主要发现:使用高通量 RT-qPCR 和 QuantStudio 12K Flex 实时 PCR 系统,评估了一组心脏恰加斯病患者(CCC I)、无症状患者(IND)和健康供体(HD)的 PBMC 中 106 个免疫相关基因在被 T. cruzi 可溶性抗原刺激后的表达情况。主成分分析(PCA)、聚类分析和火山图用于识别差异表达基因。此外,还进行了基因集富集分析(GSEA),以确定这些基因所涉及的丰富免疫途径。PCA 显示 CCC I 患者和 HD 之间与 PC1 相关的 36 个基因的表达谱存在统计学上的显著差异(p < 0.0001)。差异基因表达分析显示,与 HD 相比,CCC I 患者中有 41 个基因(表达倍数变化 > 1.5)上调,14 个基因(表达倍数变化 < 0.66)下调(p = 8.4x10-13 至 p = 0.007)。此外,在 CCC I 患者和 IND 患者之间,特定基因的表达水平也存在显著差异(8 个上调和 1 个下调)。GSEA 显示,CCC I 患者中上调的几个基因参与了免疫途径,如抗原依赖性 B 细胞激活、应激诱导的 HSP 调节、NK 细胞中的 NO2 依赖的 IL12 途径、细胞因子-炎症反应和 IL-10 抗炎信号。
心脏恰加斯病患者表现出抗原特异性的差异基因表达谱,其中一些相关免疫途径似乎被激活。评估基因表达谱可以深入了解慢性恰加斯病患者发生的免疫反应。