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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Influence of Treg cells and HBV genotype on sustained response and drug resistance in the treatment with nucleoside drugs
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Influence of Treg cells and HBV genotype on sustained response and drug resistance in the treatment with nucleoside drugs

机译:Treg细胞和HBV基因型对核苷类药物治疗持续反应和耐药性的影响

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摘要

We aimed to investigate the influence of regulatory T cells including CD4+CD25+, CD8+CD28- and hepatitis B virus (HBV) genotype on sustained virological response and tolerance of nucleoside drugs. One hundred and thirty-seven patients were enrolled. Lamivudine was administered to 84 patients. Entecavir was administered to the other 53 patients. Before treatment, biochemical tests, HBV DNA load, HBV serum level, HBV genotype, PB CD3+, CD4+, CD8+, CD4+CD25+/CD3+, and CD8+CD28-/CD3+ frequencies were measured. Based on HBV DNA loads after 4 weeks of therapy, patients were divided into response group and suboptimal response group. The lamivudine group received treatment continuously, and then patients were categorized into non-resistance group and resistance group. Compared with the suboptimal response and resistance groups for lamivudine, CD4+CD25+/CD3+ levels were higher in the response and non-resistance groups (t=4.372, P=0.046; t=7.262, P=0.017). In the non-resistance group, CD8+CD28-/CD3+ frequency was lower than in the resistance group (t=5.527, P=0.037). Virus load and hepatitis B E antigen (HBeAg)-positive rate were significantly lower than in the response and resistance group (t=2.164, P=0.038; X2=4.239, P=0.040; t=2.015, P=0.044; X2=16.2, P=0.000). Incidence of drug resistance was high in patients with virogene type C. For the virological response to entecavir, CD8+CD28-/CD3+ level was significantly lower than that of the suboptimal response group (t=6.283, P=0.036). Response and suboptimal response groups were compared in CD3+, CD4+, CD8+, CD4+CD25+/CD3+ and virus genotype, and differences were not statistically significant (P>0.05). Baseline regulatory T cells including CD4+CD25+/CD3+ and CD8+CD28-/CD3+ frequencies have a relationship with the incidence of rapid virological response and the resistance to nucleoside drugs. Patients with HBV genotype C receiving lamivudine more often underwent drug resistance. Antiviral efficacy and the resistance to lamivudine were closely correlated with baseline factors; the same cannot be found for entecavir.
机译:我们旨在研究调节性T细胞(包括CD4 + CD25 +,CD8 + CD28-和乙型肝炎病毒(HBV)基因型)对持续病毒学应答和核苷药物耐受性的影响。招募了137名患者。拉米夫定治疗84例。恩替卡韦用于其他53例患者。在治疗前,测量了生化测试,HBV DNA负载,HBV血清水平,HBV基因型,PB CD3 +,CD4 +,CD8 +,CD4 + CD25 + / CD3 +和CD8 + CD28- / CD3 +频率。根据治疗4周后的HBV DNA负荷,将患者分为反应组和次优反应组。拉米夫定组连续接受治疗,然后将患者分为非耐药组和耐药组。与拉米夫定的次优反应组和耐药组相比,反应组和非耐药组的CD4 + CD25 + / CD3 +水平更高(t = 4.372,P = 0.046; t = 7.262,P = 0.017)。在非电阻组中,CD8 + CD28- / CD3 +频率低于电阻组(t = 5.527,P = 0.037)。病毒载量和肝炎BE抗原(HBeAg)阳性率显着低于应答和耐药组(t = 2.164,P = 0.038; X2 = 4.239,P = 0.040; t = 2.015,P = 0.044; X2 = 16.2 ,P = 0.000)。 C型病毒基因患者的耐药性发生率很高。就恩替卡韦的病毒学应答而言,CD8 + CD28- / CD3 +水平显着低于次优应答组(t = 6.283,P = 0.036)。比较CD3 +,CD4 +,CD8 +,CD4 + CD25 + / CD3 +和病毒基因型的应答和次优应答组,差异无统计学意义(P> 0.05)。包括CD4 + CD25 + / CD3 +和CD8 + CD28- / CD3 +频率在内的基线调节性T细胞与快速病毒应答的发生率和对核苷药物的耐药性有关。接受拉米夫定的C基因型HBV患者更经常发生耐药性。抗病毒功效和对拉米夫定的耐药性与基线因素密切相关;对于恩替卡韦,找不到相同的结果。

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