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CD14+ monocytes and CD163+ macrophages correlate with the severity of liver fibrosis in patients with chronic hepatitis C

机译:CD14 +单核细胞和CD163 +巨噬细胞与慢性丙型肝炎患者肝纤维化的严重程度相关

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摘要

Hepatic fibrosis is a crucial pathological process involved in the development of chronic hepatitis C (CHC) and may progress to liver cirrhosis and hepatocellular carcinoma. Activated peripheral blood monocytes and intrahepatic macrophages further promote hepatic fibrogenesis by releasing proinflammatory and profibrogenic cytokines. The present study aimed to investigate the role of peripheral CD14+ monocytes and intrahepatic CD163+ macrophages in hepatitis C virus (HCV)-associated liver fibrosis and clarify whether serum soluble CD163 (sCD163) may serve as a fibrosis marker in patients with CHC. A total of 87 patients with CHC and 20 healthy controls were recruited. Serum sCD163 levels were measured by ELISA. Frequencies of peripheral CD14+ monocytes and inflammatory cytokines expressed by CD14+ monocytes were analyzed by flow cytometry. The degree of fibrosis in human liver biopsies was graded using the Metavir scoring system and patients were stratified into two groups based on those results (F<2 vs. F≥2). Hepatic expression of CD163 was examined by immunohistochemical staining. The diagnostic values of sCD163, aspartate aminotransferase to platelet ratio index (APRI), fibrosis 4 score (FIB-4) and the aspartate aminotransferase to alanine aminotransferase ratio (AAR) in significant fibrosis (F≥2) were evaluated and compared using receiver operating characteristic (ROC) curves. The results indicated that the serum sCD163 levels and the frequency of CD14+ monocytes were significantly higher in the patients than that in the controls and positively correlated with liver fibrosis. The level of serum sCD163 was consistent with hepatic CD163 expression in the liver sections from patients. The frequencies of interleukin (IL)-8- and tumor necrosis factor-α-expressing monocytes were increased and that of IL-10-expressing monocytes was decreased in the patients. The area under the ROC curve (AUROC) for sCD163, APRI, FIB-4 and AAR was 0.876, 0.785, 0.825 and 0.488, respectively, and the AUROC for sCD163 was significantly higher than those for APRI and AAR. In conclusion, sCD163 may serve as a novel marker for assessing the degree of liver fibrosis in HCV-infected patients.
机译:肝纤维化是涉及慢性丙型肝炎(CHC)的发病的关键病理过程,并且可能对肝硬化和肝细胞癌进行进展。活化外周血单核细胞和肝内巨噬细胞通过释放促炎和颅骨菌细胞因子进一步促进肝纤维发生。本研究旨在探讨外周CD14 +单核细胞和肝内CD163 +巨噬细胞在丙型肝炎病毒(HCV)的作用(HCV) - 分配的肝纤维化,并阐明血清可溶性CD163(SCD163)是否可以作为CHC患者的纤维化标志物。共招募了87例CHC和20例健康对照。通过ELISA测量血清SCD163水平。通过流式细胞术分析由CD14 +单核细胞表达的外周CD14 +单核细胞和炎性细胞因子的频率。人肝活组织检查中的纤维化程度使用Metavir评分系统进行分级,并且患者基于这些结果分为两组(F <2 Vs.2)。通过免疫组织化学染色检查CD163的肝脏表达。 SCD163,天冬氨酸氨基转移酶对血小板比指数(APRI),纤维化4分(FIB-4)和对丙氨酸氨基转移酶比(AAR)的纤维化4分(FIB-4)进行诊断值,并使用接收器进行比较特征(ROC)曲线。结果表明,患者血清SCD163水平和CD14 +单核细胞的频率显着高于对照中的患者,并与肝纤维化呈正相关。血清SCD163的水平与来自患者的肝脏部分中的肝CD163表达一致。增加了白细胞介素(IL)-8-和肿瘤坏死因子-α-表达单核细胞的频率,并且在患者中降低了IL-10的单核细胞。 SCD163,APRI,FIB-4和AAR的ROC曲线(AUROC)下的区域分别为0.876,0.785,0.825和0.488,SCD163的菌射显着高于APRI和AAR。总之,SCD163可用作评估HCV感染患者肝纤维化程度的新型标记。

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