...
首页> 外文期刊>Journal of Virological Methods >TREAT Asia Quality Assessment Scheme (TAQAS) to standardize the outcome of HIV genotypic resistance testing in a group of Asian laboratories
【24h】

TREAT Asia Quality Assessment Scheme (TAQAS) to standardize the outcome of HIV genotypic resistance testing in a group of Asian laboratories

机译:TREAT亚洲质量评估计划(TAQAS)在一组亚洲实验室中对HIV基因型耐药性测试的结果进行标准化

获取原文
获取原文并翻译 | 示例
           

摘要

The TREAT Asia (Therapeutics, Research, Education, and AIDS Training in Asia) Network is building capacity for Human Immunodeficiency Virus Type-1 (HIV-1) drug resistance testing in the region. The objective of the TREAT Asia Quality Assessment Scheme-designated TAQAS-is to standardize HIV-1 genotypic resistance testing (HIV genotyping) among laboratories to permit rigorous comparison of results from different clinics and testing centres. TAQAS has evaluated three panels of HIV-1-positive plasma from clinical material or low-passage, culture supernatant for up to 10 Asian laboratories. Laboratory participants used their standard protocols to perform HIV genotyping. Assessment was in comparison to a target genotype derived from all participants and the reference laboratory's result. Agreement between most participants at the edited nucleotide sequence level was high (>98%). Most participants performed to the reference laboratory standard in detection of drug resistance mutations (DRMs). However, there was variation in the detection of nucleotide mixtures (0-83%) and a significant correlation with the detection of DRMs (p<0.01). Interpretation of antiretroviral resistance showed similar to 70% agreement among participants when different interpretation systems were used but >90% agreement with a common interpretation system, within the Stanford University Drug Resistance Database. Using the principles of external quality assessment and a reference laboratory, TAQAS has demonstrated high quality HIV genotyping results from Asian laboratories.
机译:TREAT亚洲(亚洲的治疗,研究,教育和艾滋病培训)网络正在为该地区的1型人类免疫缺陷病毒(HIV-1)耐药性测试建立能力。由TREAT Asia质量评估计划指定的TAQAS的目标是标准化实验室之间的HIV-1基因型耐药性测试(HIV基因分型),以允许严格比较不同诊所和测试中心的结果。 TAQAS已对多达10个亚洲实验室的临床材料或低通量培养上清液评估了3组HIV-1阳性血浆。实验室参与者使用他们的标准方案进行HIV基因分型。评估与从所有参与者和参考实验室的结果得出的目标基因型进行比较。在核苷酸序列编辑水平上,大多数参与者之间的一致性很高(> 98%)。大多数参与者在检测耐药性突变(DRM)时都遵循参考实验室标准。但是,核苷酸混合物的检测存在差异(0-83%),与DRM的检测存在显着相关性(p <0.01)。在斯坦福大学药物耐药性数据库中,使用不同的解释系统时,抗逆转录病毒药物耐药性的解释显示参与者之间的一致性接近70%,但与通用解释系统的一致性> 90%。利用外部质量评估的原理和参考实验室,TAQAS已经证明了来自亚洲实验室的高质量HIV基因分型结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号