Department of Viral Hepatitis, University Hospital for Infectious Diseases Zagreb, Zagreb, Croatia.
University of Zagreb, School of Medicine, Zagreb, Croatia.
PLoS One. 2018 Dec 28;13(12):e0209481. doi: 10.1371/journal.pone.0209481. eCollection 2018.
Semaphorins are a diverse family of immunoregulators recently recognized to play a major role in various phases of immune responses. Their role in chronic viral hepatitis C (CHC) and contribution to the progression of liver disease is unknown. The aim of this study was to analyse the association of secreted semaphorins with the severity of liver disease in patients with CHC. Serum concentrations of semaphorins were measured in 114 treatment-naive CHC patients and 36 healthy controls. Serum concentrations of SEMA3A, SEMA3C, SEMA5A, SEMA6B and SEMA6D were significantly increased in patients with CHC compared to controls. While serum concentrations of SEMA3C and SEMA6D significantly increased with fibrosis stage in both HCV-g1 and HCV-g3 infections, the concentration of SEMA5A inversely correlated with fibrosis stage in both HCV genotypes. ROC analysis showed that serum concentrations of SEMA3C (>4.0ng/mL, AUC 0.88) and SEMA6D (>4.5, AUC 0.82) had higher AUC than widely used APRI (AUC 0.71) and FIB-4 (AUC 0.74) scores. Serum concentrations of SEMA3C and SEMA6D significantly decreased after DAA and PEG IFN-α/ribavirin therapy, while the serum concentration of SEMA5A significantly increased after DAAs therapy. Immunohistochemistry confirmed the expression of SEMA3C and SEMA5A in hepatocytes, endothelial cells and lymphocytes of cirrhotic livers from CHC patients but not in controls. In conclusion, we provide the first evidence that SEMA3C, SEMA5A and SEMA6D can be considered as markers of liver injury in CHC.
信号素是一类新发现的免疫调节因子,其家族成员众多,在各种免疫反应阶段发挥着重要作用。目前,信号素在慢性丙型肝炎(CHC)中的作用及其对肝脏疾病进展的影响尚不清楚。本研究旨在分析分泌型信号素与 CHC 患者肝脏疾病严重程度的相关性。我们检测了 114 例未经治疗的 CHC 患者和 36 例健康对照者的血清信号素浓度。与对照组相比,CHC 患者的血清 SEMA3A、SEMA3C、SEMA5A、SEMA6B 和 SEMA6D 浓度显著升高。在 HCV-g1 和 HCV-g3 感染中,血清 SEMA3C 和 SEMA6D 浓度随着纤维化分期的增加而显著升高,而 SEMA5A 浓度则与两种 HCV 基因型的纤维化分期呈负相关。ROC 分析显示,SEMA3C(>4.0ng/ml,AUC 0.88)和 SEMA6D(>4.5,AUC 0.82)的血清浓度比广泛使用的 APRI(AUC 0.71)和 FIB-4(AUC 0.74)评分具有更高的 AUC。在 DAA 和 PEG IFN-α/利巴韦林治疗后,SEMA3C 和 SEMA6D 的血清浓度显著降低,而在 DAA 治疗后,SEMA5A 的血清浓度显著升高。免疫组化证实了 SEMA3C 和 SEMA5A 在 CHC 患者肝硬化肝组织中肝细胞、内皮细胞和淋巴细胞中的表达,但在对照组中没有表达。总之,我们首次证明 SEMA3C、SEMA5A 和 SEMA6D 可作为 CHC 肝损伤的标志物。