《使用一套耐药基因型的内部测试系统找出香港人类免疫缺陷病毒1型高效抗逆转录病毒治疗耐药基因的变异情况》

  • 来源专题:艾滋病防治
  • 编译者: 李越
  • 发布时间:2012-03-13
  • Objective To determine the frequency of highly active antiretroviraltherapy resistance mutations in the viral pol gene of humanimmunodeficiency virus–1 (HIV-1) genotypes that circulate inHong Kong, by means of an in-house HIV-1 genotyping system.Design Retrospective study.Setting Two HIV clinics in Hong Kong.Patients A modified in-house genotyping resistance test was used tosequence the partial pol gene in 1165 plasma samples from 965patients. The performance of our test was cross-compared withthe US Food and Drug Administration–approved ViroSeq HIV-1genotyping system. The results of genotyping were submitted tothe Stanford HIV-1 drug resistance database for analysis.Results The cost-effective in-house genotypic resistance test (US$40)demonstrated comparable performance to the US Food andDrug Administration–approved ViroSeq system. The detectionlimit of this in-house genotypic resistance test could reach 400copies/mL for both HIV-1 subtype B and CRF01_AE, which werethe predominant genotypes in Hong Kong. Drug resistancemutations were detected only in post-treatment samples fromtreatment-failure patients. However, there was no significantdifference in the frequency of drug resistance mutations betweensubtype B and CRF01_AE.Conclusion Our cost-effective in-house genotypic resistance test detectedno significant difference in drug resistance–related mutationsfrequencies between HIV-1 subtype B and CRF01_AE in HongKong. A drug resistance–related mutations database for differentHIV-1 genotypes should be established in Hong Kong to augmentguidance for HIV treatment.
  • 原文来源:http://www.hkmj.org/article_pdfs/hkm1202p20.pdf
相关报告
  • 《河南省人类免疫缺陷病毒-1型耐药毒株的变异情况研究》

    • 来源专题:艾滋病防治
    • 编译者:李越
    • 发布时间:2012-12-26
    • 了解河南省经过抗病毒治疗5年后人类免疫缺陷病毒-1型(human immunodeficiency virus-1, HIV-1 )耐药毒株的变异情况。方法通过横断面调查,参照WHO提供的标准,采集2007年11月到2008年8月间新确认的2~25岁未经抗病毒治疗的艾滋病感染者血清69例,用逆转录聚合酶链式反应(RT—PCR)方法扩增HIV-1pol区基因,进行基因型耐药性分析。结果69份调查样本中,扩增并测序成功50份,在逆转录酶(RT)区检测到7个耐药突变位点,蛋白酶(PR)区检测出3个次要耐药突变位点,但仅在逆转录酶区发现1份样本(K103N突变)出现针对非核苷类抑制剂(NNRTIs)高度耐药,蛋白酶区未检测到对蛋白酶抑制剂的高度耐药。根据HIV耐药警戒线监测抽样表河南省HIV-1耐药毒株的流行率〈5%。结论河南省HIV-1耐药株的传播尚处于低度流行水平。但随着抗病毒治疗时间的延长耐药株出现的比例增高,需要密切关注耐药株的传播问题并继续进行此类耐药性监测工作。
  • 《人类白细胞抗原多态性与人类免疫缺陷病毒患者抗逆转录病毒治疗超敏反应的关联:Meta分析》

    • 来源专题:艾滋病防治
    • 编译者:张玢
    • 发布时间:2019-07-12
    • 白细胞抗原(HLA)等位基因涉及药物诱导的超敏反应,包括奈韦拉平和阿巴卡韦。该荟萃分析的目的是评估HLA多态性与人类免疫缺陷病毒(HIV)感染患者对抗逆转录病毒治疗的超敏反应之间的关系。对PubMed,Embase,Web of Science和Cochrane图书馆进行了系统检索,以评估2019年4月发表的HLA多态性与抗逆转录病毒疗法诱导的超敏反应的关联。概率比值(OR)与95%置信区间(CIs)被认为是对效果的估计。荟萃分析包括17项研究,共评估了4273名患者。首先,HLA-A * 24携带者与接受抗逆转录病毒治疗的HIV患者的超敏反应风险增加相关(OR:12.12; P = 0.018)。第二,HLA-B基因型的5个SNP,包括* 18(OR:1.63; P = 0.028),* 35(OR:2.31; P = 0.002),* 39(OR:11.85; P = 0.040),* 51( OR:1.66; P = 0.028),* 81(OR:8.11; P = 0.021)与过敏风险增加有关。相反,HLA-B * 15携带者的超敏反应风险降低(OR:0.43; P <0.001)。第三,HLA-C * 04与过敏风险增加相关(OR:3.09; P <0.001),而HLA-C * 02携带者患者的超敏反应风险较低(OR:0.22; P = 0.030),* 03(OR:0.53; P = 0.049),和* 07(OR:0.61; P = 0.044)。最后,HLA-DRB1 * 05(OR:0.18; P = 0.006)和* 15(OR:0.23; P = 0.013)的携带者与接受抗逆转录病毒疗法的患者的超敏反应风险降低相关。该荟萃分析的结果表明携带HLA-A * 24,HLA-B * 18,* 35,* 39,* 51,* 81,HLA-C * 04的患者具有较高的超敏反应风险。相反,携带HLA-B * 15,HLA-C * 02,* 03,* 07,HLA-DRB1 * 05,* 15的受试者与降低的超敏反应风险相关。