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Cross-linking of CD81 by HCV-E2 protein inhibits human intrahepatic plasmacytoid dendritic cells response to CpG-ODN

机译:HCV-E2蛋白使CD81交联抑制人肝内浆细胞样树突状细胞对CpG-ODN的反应

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Plasmacytoid dendritic cells (pDCs) are reported to be defective in HCV-infected patients, the mechanisms of which remain poorly understood. We isolated liver derived mononuclear cells (LMNCs) and pDCs from normal liver tissues of benign tumor dissections and liver transplant donors. Isolated pDCs and LMNCs were cultured with precoated HCV envelop protein E2 (HCV-E2) or anti-CD81 mAb in the presence of CpG-ODN. Our results show that cross-linking of CD81 by either HCV-E2 or anti-CD81 mAb inhibits IFN-α secretion in CpG-induced pDCs; down-regulates HLA-DR, CD80 and CD86 expression in pDCs; and suppresses CpG-ODN induced proliferation and survival of pDCs. The blockade of CD81 by soluble anti-CD81 antibody restores pDCs response to CpG-ODN. These results suggest that HCV E2 protein interacts with CD81 to inhibit pDC maturation, activation, and IFN-α production, and may thereby contribute to the impaired innate anti-viral immune response in HCV infection.
机译:据报道,在HCV感染的患者中,浆细胞样树突状细胞(pDCs)存在缺陷,其机制尚不清楚。我们从良性肿瘤清扫的正常肝组织和肝移植供体中分离出肝来源的单核细胞(LMNC)和pDC。在CpG-ODN存在的情况下,将分离的pDC和LMNC与预包被的HCV包膜蛋白E2(HCV-E2)或抗CD81 mAb培养。我们的研究结果表明,HCV-E2或抗CD81 mAb与CD81发生交联会抑制CpG诱导的pDC中IFN-α的分泌。下调pDC中的HLA-DR,CD80和CD86表达;并抑制CpG-ODN诱导的pDC增殖和存活。可溶性抗CD81抗体对CD81的阻断可恢复pDC对CpG-ODN的反应。这些结果表明,HCV E2蛋白与CD81相互作用以抑制pDC的成熟,激活和IFN-α的产生,从而可能导致HCV感染中先天性抗病毒免疫应答受损。

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