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Effect of HCV core and core+1/S on pro- and anti-inflammatory cytokine and chemokine gene expression

机译:HCV核心和核+ 1 / s对抗炎细胞因子和趋化因子基因表达的影响

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Pro- (IL6, TNFalpha) and anti-inflammatory (IL-10) cytokines and chemokines (MIP-1beta, IL8, MCP-1) may play a pivotal role in the development of inflammation that characterises chronic HCV infection. The HCV core protein has been implicated in modulating host immune response, nevertheless this may be attributed partly to the newly discovered core+1 protein, overlapping the core sequence. A putative effect of core and core+1 on cytokine and chemokine gene expression in both immune and hepatic cells, could account for the establishment of chronic inflammation in HCV patients. This study reports altered cytokine and chemokine mRNA levels in hepatoma cells and macrophages in which core and core+1/S have been ectopically expressed.
机译:Pro-(IL6,TNFalpha)和抗炎(IL-10)细胞因子和趋化因子(MIP-1Beta,IL8,MCP-1)可能在表征慢性HCV感染的炎症的发育中发挥枢转作用。 HCV核心蛋白已涉及调节宿主免疫应答,然而这可能部分地归因于新发现的核+ 1蛋白,重叠核心序列。核心和核心+ 1对免疫和肝细胞中细胞因子和趋化因子基因表达的调整作用,可以考虑在HCV患者中建立慢性炎症。本研究报告了肝癌细胞中的细胞因子和趋化因子mRNA水平和巨噬细胞的巨噬细胞,其中核心和核心+ 1 / s被异化表达。

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