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Serum cytokine levels in patients with chronic hepatitis B according to lamivudine therapy.

机译:根据拉米夫定治疗的慢性乙型肝炎患者血清细胞因子水平。

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BACKGROUND: Cytokines are known to play critical roles in the pathogenesis of chronic hepatitis B (CHB). However, the relationship between cytokines and treatment responses to drugs for CHB is not clearly defined yet. We measured the serum cytokine levels of interleukin (IL)-1alpha, IL-1beta, IL-2, IL-4, IL-6, IL-8, IL-10, vascular endothelial growth factor, interferon-gamma, tumor necrosis factor- (TNF-alpha), macrophage/monocyte chemotactic protein 1, and epidermal growth factor to elucidate the cytokine expression pattern according to the patients' responses to lamivudine. METHODS: Fifty-eight specimens from 27 CHB patients and 98 specimens from healthy individuals were tested for 12 kinds of cytokines. The patients were grouped as: before treatment, ongoing treatment, duringmaintaining remission, and patients with viral breakthrough owing to resistance against lamivudine. The Evidence Investigator (Randox, Antrim, UK), a protein chip analyzer, was used to quantify serum cytokines. RESULTS: Among 12 cytokines, IL-6, IL-8, IL-10, and TNF-alpha were significantly elevated in patients with resistance against lamivudine compared with patients maintaining response. IL-8, IL-10, and TNF-alpha levels also weak to moderate correlated with ALT and HBV-DNA concentrations. CONCLUSIONS: Serum cytokine levels would reflect the pathological differences of the individual treatment phases and may become useful indices in monitoring the treatment response of CHB.
机译:背景:已知细胞因子在慢性乙型肝炎(CHB)的发病机理中起关键作用。但是,目前尚不清楚细胞因子与CHB药物治疗反应之间的关系。我们测量了白细胞介素(IL)-1alpha,IL-1beta,IL-2,IL-4,IL-6,IL-8,IL-10,血管内皮生长因子,干扰素-γ,肿瘤坏死因子的血清细胞因子水平-(TNF-α),巨噬细胞/单核细胞趋化蛋白1和表皮生长因子,根据患者对拉米夫定的反应来阐明细胞因子的表达方式。方法:对27例CHB患者的58份标本和健康人的98份标本进行了12种细胞因子的检测。患者分为:治疗前,进行中的治疗,维持缓解期间的患者以及因对拉米夫定耐药而出现病毒突破的患者。证据调查器(Randox,Antrim,英国)是一种蛋白质芯片分析仪,用于定量血清细胞因子。结果:在12种细胞因子中,与维持反应的患者相比,对拉米夫定耐药的患者的IL-6,IL-8,IL-10和TNF-α显着升高。 IL-8,IL-10和TNF-α水平也弱至中度与ALT和HBV-DNA浓度相关。结论:血清细胞因子水平将反映各个治疗阶段的病理学差异,并可能成为监测CHB治疗反应的有用指标。

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