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细胞免疫功能对乙型肝炎病毒复制及抗病毒治疗的意义 被引量:11
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作者 孟存仁 杨立 +1 位作者 王家路 张朝霞 《中国全科医学》 CAS CSCD 北大核心 2010年第20期2226-2229,共4页
目的分析乙型肝炎病毒(HBV)复制、转归及变异与细胞免疫功能的关系。方法检测37例慢性乙型肝炎(乙肝)患者(慢性乙肝组)、20例HBV携带者(无症状携带组)、36例乙肝肝硬化患者(乙肝肝硬化组)及24例健康体检者(正常对照组)的外周血T细胞亚群... 目的分析乙型肝炎病毒(HBV)复制、转归及变异与细胞免疫功能的关系。方法检测37例慢性乙型肝炎(乙肝)患者(慢性乙肝组)、20例HBV携带者(无症状携带组)、36例乙肝肝硬化患者(乙肝肝硬化组)及24例健康体检者(正常对照组)的外周血T细胞亚群,分析HBV不同感染状况者T细胞亚群的差异;用实时荧光定量PCR法检测HBV感染者HBV-DNA水平和拉米夫定相关变异(YMDD)。结果 (1)与正常对照组比较,无症状携带组和慢性乙肝组的CD3+、CD4+T细胞的百分比和计数均显著降低(P<0.05),无症状携带者的CD8+T细胞计数亦显著低于正常对照组(P<0.05),而两组的CD8+T细胞百分比及CD4+/CD8+比值与正常对照组比较,差异均无统计学意义(P>0.05);乙肝肝硬化组CD4+T细胞百分比与正常对照组比较,差异无统计学意义(P>0.05),但CD4+/CD8+比值显著高于正常对照组,CD3+、CD4+、CD8+T细胞计数均显著低于其他各组,差异有统计学意义(P<0.05)。(2)HVB感染者HBV-DNA水平与外周血CD3+、CD4+、CD8+T细胞及CD4+/CD8+比值无相关性(P>0.05)。(3)抗病毒治疗6个月后HBV-DNA水平小于检测低限组的外周血CD3+、CD4+、CD8+T细胞计数显著高于治疗12个月后转归及无转归组,而CD4+/CD8+比值显著低于治疗12个月后无转归组,差异均有统计学意义(P<0.05)。(4)拉米夫定相关变异型和野生型HBV感染者外周血CD3+、CD4+、CD8+T细胞及CD4+/CD8+比值间差异无统计学意义(P>0.05)。结论慢性HBV感染者体内存在T细胞亚群失衡和细胞免疫功能紊乱,可能是HBV感染后慢性化的重要原因;T细胞亚群检测可作为抗病毒治疗效果和疾病转归的预测指标;T细胞亚群计数较百分比更能反映患者的细胞免疫状况。 展开更多
关键词 肝炎病毒 乙型 病毒复制 肝炎 乙型 慢性 肝硬化 T淋巴细胞 拉米夫定相关变异
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拉米夫定治疗慢性乙型肝炎中变异病毒株的动态变化 被引量:5
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作者 田国保 席宏丽 +4 位作者 田地 崔建军 于敏 陆海英 曾争 《世界华人消化杂志》 CAS 北大核心 2007年第30期3245-3250,共6页
目的:建立定量检测及监测乙肝病毒DNA的rtM204I/V(YMDD)及rtL180M变异的方法.方法:以克隆、测序鉴定及构建乙肝病毒DNA YMDD及变异(YIDD和YVDD)质粒作为标准,4例接受拉米夫定治疗(100 mg/d,疗程48 wk以上)的慢性乙型肝炎患者血清标本为... 目的:建立定量检测及监测乙肝病毒DNA的rtM204I/V(YMDD)及rtL180M变异的方法.方法:以克隆、测序鉴定及构建乙肝病毒DNA YMDD及变异(YIDD和YVDD)质粒作为标准,4例接受拉米夫定治疗(100 mg/d,疗程48 wk以上)的慢性乙型肝炎患者血清标本为对象,用焦磷酸测序的方法检测变异位点核苷酸的频率,并计算变异株的含量比例,通过检测不同变异株类型的标准质粒,确定测序峰图的背景信号.结果:通过检测标准质粒后,确定背景信号为5%,变异位点调整后的核苷酸频率转化为变异病毒株的比例后,4例患者治疗前均检测出变异的病毒株(4.5%-33%),并且随治疗时间延长呈增多的趋势.病毒载量及ALT分析提示基因型耐药发生后,将发生病毒学反跳及临床耐药.结论:焦磷酸测序可以定量检测及动态监测变异病毒株的含量.拉米夫定耐药突变株在拉米夫定治疗前已存在,并随治疗时间的增加而增长,出现病毒学反弹及临床耐药. 展开更多
关键词 焦磷酸测序 拉米夫定 治疗 慢性乙型肝炎 变异病毒株 动态变化
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拉米夫定和苦参碱治疗伴高胆红素血症的慢性乙型肝炎临床观察 被引量:5
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作者 陈从新 刘波 +3 位作者 杨家宏 刘克万 徐宁 宋海燕 《实用肝脏病杂志》 CAS 2009年第4期256-261,共6页
目的研究拉米夫定联合苦参碱治疗伴高胆红素血症的慢性乙型肝炎的疗效。方法在232例伴高胆红素血症的慢性乙型肝炎患者中,包括慢性乙型肝炎重度无明显消化道症状者(A1组)70例和有明显消化道症状者(A2组)58例,慢性乙型重型肝炎基础肝病... 目的研究拉米夫定联合苦参碱治疗伴高胆红素血症的慢性乙型肝炎的疗效。方法在232例伴高胆红素血症的慢性乙型肝炎患者中,包括慢性乙型肝炎重度无明显消化道症状者(A1组)70例和有明显消化道症状者(A2组)58例,慢性乙型重型肝炎基础肝病为慢性HBV携带者(B1组)22例、慢性乙型肝炎(B2组)34例和肝硬化(B3组)48例。在基础治疗的基础上,各组患者均给予拉米夫定口服和苦参碱静脉滴注治疗,另给予A2、B1和B2组患者氢化可的松琥珀酸钠短程治疗。结果经过3~4周治疗,A1和A2组患者均获得临床和生化学痊愈,而在B1组有4例(18.2%)、B2组有9例(26.5%)和B3组有18例(37.5%)患者死亡;入院时,B1组患者HBeAg阳性率为90.0%,B3组以抗-HBe阳性为主(91.7%),B1组患者HBVDNA水平(lg7.2±1.4 copies/ml)最高,而B3组患者HBV DNA水平(lg5.4±0.9 copies/ml,P<0.01)较低;在各组存活者中,90%以上HBV DNA转阴,B2和B1组患者血清HBeAg/抗-Hbe转换率分别为72.3%(8/11)和27.8%(5/18);典型患者的腹部CT复查显示腹水消退,缩小的肝脏增大;两次肝活组织病理学检查显示Knodell’HAI计分明显改善。结论以拉米夫定联合苦参碱为基础的治疗对伴有高胆红素血症的慢性乙型肝炎患者有效。 展开更多
关键词 慢性乙型肝炎 高胆红素血症 拉米夫定 苦参碱
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Safety of lamivudine treatment for chronic hepatitis B in early pregnancy 被引量:29
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作者 Wei Yi Min Liu Hao-Dong Cai 《World Journal of Gastroenterology》 SCIE CAS CSCD 2012年第45期6645-6650,共6页
AIM:To evaluate the safety of lamivudine(LAM) treatment for chronic hepatitis B in early pregnancy.METHODS:A total of 92 pregnant women who received LAM treatment either before pregnancy or in early pregnancy were enr... AIM:To evaluate the safety of lamivudine(LAM) treatment for chronic hepatitis B in early pregnancy.METHODS:A total of 92 pregnant women who received LAM treatment either before pregnancy or in early pregnancy were enrolled in this study.All of the pregnant women volunteered to take lamivudine during pregnancy and were not co-infected with hepatitis C virus,human immunodeficiency virus,cytomegalovirus,or other viruses.All infants received passiveactive immunoprophylaxis with 200 IU hepatitis B immunoglobulin and three doses of 10 μg hepatitis B vaccines(0-1-6 mo) according to the guidelines for the prevention and treatment of chronic hepatitis B.Adverse events were observed throughout the entire pregnancy and perinatal period,and the effectiveness of lamivudine treatment for blocking mother-to-infant transmission of hepatitis B virus(HBV) was evaluated.All adverse events in mothers and infants during pregnancy and the perinatal period and the HBV motherto-infant transmission blocking rate were compared with the literature.RESULTS:Among the 92 pregnant women,spontaneous abortions occurred in 11 cases,while 3 mothers had a second pregnancy after the initial abortion;72 mothers delivered 73 live infants,of whom 68 infants were followed up for no less than 6 mo,and 12 mothers were still pregnant.During pregnancy,the main maternal adverse events were vaginitis(12/72,16.7%),spontaneous abortion(11/95,11.6%),and gestational diabetes(6/72,8.3%);only one case had 1-2 degree elevation of the creatine kinase level(195 U/L).During the perinatal period,the main maternal adverse events were premature rupture of the membranes(8/72,11.1%),preterm delivery(5/72,6.9%),and meconium staining of the amniotic fluid(4/72,5.6%).In addition,2 infants were found to have congenital abnormalities;1 had a scalp hemangioma that did not change in size until 7 mo,and the other had early cerebral palsy,but with rehabilitation training,the infant's motor functions became totally normal at 2 years of age.The incidence of adverse events among the mothers or abnormalities in the infants was not higher than that of normal mothers or HBV-infected mothers who did not receive lamivudine treatment.In only 2 cases,mother-to-infant transmission blocking failed;the blocking rate was 97.1%(66/68),which was higher than has been previously reported.CONCLUSION:Lamivudine treatment is safe for chronic HBV-infected pregnant mothers and their fetuses with a gestational age of less than 12 wk or throughout the entire pregnancy. 展开更多
关键词 慢性乙型肝炎 怀孕期间 拉米夫定 治疗 安全 丙型肝炎病毒 人类免疫缺陷病毒 合并感染
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