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首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Interaction between Galectin-9/TIM-3 pathway and follicular helper CD4 + T cells contributes to viral persistence in chronic hepatitis C
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Interaction between Galectin-9/TIM-3 pathway and follicular helper CD4 + T cells contributes to viral persistence in chronic hepatitis C

机译:Galectin-9 / Tim-3途径和滤泡辅助CD4 + T细胞之间的相互作用有助于慢性丙型肝炎的病毒持久性

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Abstract Both Galectin 9 (Gal-9)/T-cell immunoglobulin and mucin domain-containing protein 3 (TIM-3) pathway and follicular helper CD4 + T (Tfh) cells play important roles in persistent hepatitis C virus (HCV) infection. Thus, we aimed to investigate the regulatory role of interaction between Gal-9/TIM-3 pathway and Tfh cells in chronic hepatitis C. A total of 44 chronic hepatitis C patients and 19 normal controls (NCs) were enrolled in this study. Purified CD4 + T cells were cultured by TIM-3 Fc protein, recombinant Gal-9, or IL-21 for 48 h. TIM-3 expression, Tfh proportion, and IL-21 production was measured, respectively. The immunomodulatory role of Gal-9/TIM-3 and IL-21 was also investigated in HCV cell culture system in vitro . We found that the percentage corresponding to both TIM-3-positive and CXCR5 + ICOS + Tfh cells within CD4 + T cells, which correlated with HCV RNA replication, was significantly elevated in patients with chronic hepatitis C in comparison with those in NCs. Moreover, blockade of Gal-9/TIM-3 pathway by TIM-3 Fc protein increased Tfh cells proportion, IL-21 mRNA and protein expression within purified CD4 + T cells, while activation of Gal-9/TIM-3 signaling by Gal-9 stimulation decreased IL-21 production in both patients with chronic HCV infection and healthy individuals. Meanwhile, high concentrations (100 and 200 ng/mL) of IL-21 stimulation also elevated TIM-3 expression on CD4 + T cells in chronic hepatitis C. Furthermore, TIM-3 blockage and IL-21 stimulation suppressed mRNA expressions of HCV-induced antiviral proteins (myxovirus resistance A and oligoadenylate synthetase) in Huh7.5 cells without affecting viral replication in HCV cell culture system. The interaction between Gal-9/TIM-3 pathway and Tfh cells contributed to viral persistent in chronic HCV infection, which might be pivotal for development of new therapeutic approaches for chronic hepatitis C. ]]>
机译:摘要Galectin 9(GAL-9)/ T细胞免疫球蛋白和含粘膜域的蛋白3(TIM-3)途径和滤泡辅助CD4 + T(TFH)细胞在持续的丙型肝炎病毒(HCV)感染中起重要作用。因此,我们旨在研究慢性丙型肝炎GAL-9 / TIM-3途径和TFH细胞之间相互作用的调节作用。共有44例慢性丙型肝炎患者和19例正常对照(NCS)。纯化的CD4 + T细胞被TIM-3 Fc蛋白,重组加仑-9或IL-21培养48小时。分别测量TIM-3表达,TFH比例和IL-21产生。在HCV细胞培养系统中,还在体外研究了GAL-9 / TIM-3和IL-21的免疫调节作用。我们发现,与HCV RNA复制相关的CD4 + T细胞中对应于TIM-3阳性和CXCR5 + ICOS + TFH细胞的百分比,慢性丙型肝炎患者与NCS中的患者显着升高。此外,通过TIM-3 Fc蛋白的Gal-9 / Tim-3途径增加了TFH细胞比例,IL-21 mRNA和蛋白表达在纯化的CD4 + T细胞内,同时通过GAL激活GAL-9 / TIM-3信号传导-9刺激在慢性HCV感染和健康个体患者中降低了IL-21产生。同时,IL-21刺激的高浓度(100和200ng / ml)也升高了慢性丙型肝炎CD4 + T细胞上的TIM-3表达。此外,TIM-3堵塞和IL-21刺激抑制了HCV的mRNA表达Huh7.5细胞中诱导抗病毒蛋白(骨甲病毒A和寡核苷酸合成酶)而不影响HCV细胞培养系统中的病毒复制。 GAL-9 / TIM-3通路和TFH细胞之间的相互作用导致慢性HCV感染中的病毒持续性,这可能是慢性丙型肝炎新治疗方法的关键态度。]]]

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