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Chronic immune activation is a distinguishing feature of liver and PBMC gene signatures from HCV/HIV coinfected patients and may contribute to hepatic fibrogenesis

机译:慢性免疫激活是来自HCV / HIV繁殖患者的肝脏和PBMC基因特征的显着特征可能有助于肝纤维发生

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摘要

Hepatitis C virus/human immunodeficiency virus (HCV/HIV) coinfected patients demonstrate accelerated progression to severe liver injury in comparison to HCV monoinfected patients, although the underlying mechanisms are unclear owing to infection of separate tissue compartments with two distinct viral pathogens. Microarray analysis of paired liver biopsy and peripheral blood mononuclear cell (PBMC) specimens from HCV/HIV coinfected and HCV monoinfected patients identified a gene expression signature associated with increased inflammation and immune activation that was present only in liver and PBMC samples from coinfected patients. We also identified in these samples liver- and PBMC-specific signatures enriched with fibrogenic/hepatic stellate activation and proinflammatory genes, respectively. Finally, Bayesian networks were constructed by assimilating these data with existing data from liver and PBMC samples from other cohorts, augmenting enrichment of biologically important pathways and further indicating that chronic immune activation in HCV/HIV coinfection may exacerbate liver disease progression in coinfected patients.
机译:丙型肝炎病毒/人类免疫缺陷病毒(HCV / HIV)繁殖患者与HCV单染型患者相比,对严重肝损伤的加速进展表现出对严重的肝损伤,尽管由于具有两个不同的病原病原体的单独组织隔间,潜在的机制尚不清楚。来自HCV / HIV的配对肝活检和外周血单核细胞(PBMC)标本的微阵列分析来自HCV / HIV焦和HCV单培养患者的基因表达签名与仅在来自辛感染患者的肝脏和PBMC样品中存在的炎症和免疫活化相关的基因表达签名。我们还在这些样品中鉴定在富含纤维纤维/肝星状激活和促炎基因的肝脏和PBMC特异性鉴定。最后,通过将这些数据与来自其他群组的肝脏和PBMC样本的现有数据同化,通过来自其他队列的现有数据,增强生物学上重要途径的富集以及进一步表明HCV / HIV辛凝集的慢性免疫激活可以加剧肝脏疾病进展的浓缩患者中的慢性免疫活化。

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