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Long-Term Effect on Natural Killer Cells by Interferon-α Therapy on the Outcomes of HCV Infection

机译:干扰素-α疗法对HCV感染结果对自然杀伤细胞的长期影响

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摘要

Natural killer (NK) cells act as innate immune cells against hepatitis C virus (HCV) infection. Interferon-α (IFN-α) and ribavirin are the standard treatments for patients with HCV infection. This study is aimed at investigating the dynamic changes in the frequency of different subsets of NK cells following treatment in xx chronic hepatitis C (CHC) patients. CHC patients were treated with peg-IFN or IFN-α, and followed up for 72 weeks. The frequency of different subsets of NK in CHC patients was determined longitudinally by flow cytometry. Treatment with the standard therapy increased the percentages of NKp30+, NKp46+, and CD107a+ NK cells, which were positively correlated with the declining of serum HCV-RNA, but not IFN-γ+ NK cells. NKG2A+ and KIR2DL3+ NK cells were associated with an early virological response in CHC patients. Treatment with IFN-α adjusts the balance of activated receptors and inhibitory receptors and enhances the cytotoxic activity of NK cells. Therefore, measuring NK subsets may be valuable for therapeutic responses in CHC patients.
机译:自然杀手(NK)细胞可作为抵抗丙型肝炎病毒(HCV)感染的先天免疫细胞。干扰素-α(IFN-α)和利巴韦林是HCV感染患者的标准治疗方法。这项研究旨在调查xx慢性丙型肝炎(CHC)患者接受治疗后NK细胞不同亚群频率的动态变化。 CHC患者接受peg-IFN或IFN-α治疗,随访72周。通过流式细胞术纵向确定了CHC患者中NK不同亚群的频率。用标准疗法治疗可增加NKp30 + ,NKp46 + 和CD107a + NK细胞百分比,与NK细胞的下降呈正相关血清HCV-RNA,而不是IFN-γ + NK细胞。 NKG2A + 和KIR2DL3 + NK细胞与CHC患者的早期病毒学应答有关。 IFN-α的治疗可调节活化受体和抑制受体的平衡,并增强NK细胞的细胞毒活性。因此,测量NK亚群可能对CHC患者的治疗反应有价值。

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