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首页> 外文期刊>Journal of Clinical Microbiology >Discordance between Genotypic and Phenotypic Drug Resistance Profiles in Human Immunodeficiency Virus Type 1 Strains Isolated from Peripheral Blood Mononuclear Cells
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Discordance between Genotypic and Phenotypic Drug Resistance Profiles in Human Immunodeficiency Virus Type 1 Strains Isolated from Peripheral Blood Mononuclear Cells

机译:从外周血单个核细胞中分离出的人类免疫缺陷病毒1型菌株的基因型和表型耐药性谱之间的不一致。

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The aim of the study was to analyze the relationship between genotypic and phenotypic drug resistance profiles of human immunodeficiency virus type 1 (HIV-1) strains isolated from patients during double-analogue nucleoside therapy. A drug-resistant HIV strain was isolated from 20 out of 25 patients, with 16 (64%) subjects carrying a virus with multiple drug resistance mutations. The most frequent resistance mutations were M184V (18 isolates) and M41L (7 isolates). Discordance between the genotypic and phenotypic profile for at least one drug was detected in 16 out of 25 strains. Particularly, eight isolates had a discordant genotypic-phenotypic resistance pattern for two drugs and one isolate had such a pattern for three drugs. A genotypic resistance pattern with a phenotypic sensitivity profile was detected in six isolates (four resistant to zidovudine and two resistant to lamivudine). On the other hand for several strains a genotypic pattern of sensitivity pattern to abacavir (10 strains), didanosine (7 strains), stavudine (3 strains), zidovudine (2 strains), and lamivudine (1 strain) with a phenotypic resistance profile was detected. After a follow-up period of 8 months, an impairment of virological and immunological parameters was detected only in subjects with an HIV-1 isolate with a phenotypic resistance profile in despite of the genotypic results. Predicting resistance phenotype from genotypic data has important limitations. Despite the low number of patients and the short follow-up period, this study suggests that during failing therapy with analogue nucleosides, a phenotypic analysis could be performed in spite of an HIV genotypic sensitivity pattern.
机译:该研究的目的是分析从双模拟核苷治疗中分离出的患者的人类免疫缺陷病毒1型(HIV-1)菌株的基因型和表型耐药性之间的关系。从25名患者中的20名患者中分离出一种耐药HIV毒株,其中16名(64%)受试者携带带有多种耐药突变的病毒。最常见的耐药突变是M184V(18个分离株)和M41L(7个分离株)。在25个菌株中的16个中检测到至少一种药物的基因型和表型特征之间的不一致。特别地,八种分离物对两种药物具有不一致的基因型-表型抗性模式,而一种分离物对三种药物具有这种模式。在六个分离株(四个对齐多夫定耐药和两个对拉米夫定耐药)中检测到具有表型敏感性特征的基因型耐药模式。另一方面,对于几种菌株,具有对表型耐药性的对阿巴卡韦(10株),去羟肌苷(7株),司他夫定(3株),齐多夫定(2株)和拉米夫定(1株)的敏感性模式的基因型为。检测到。经过8个月的随访,尽管有基因型结果,但仅在具有表型耐药性的HIV-1分离物受试者中检测到病毒学和免疫学参数受损。从基因型数据预测耐药性表型具有重要的局限性。尽管患者人数少且随访时间短,但这项研究表明,在使用类似核苷的治疗失败的情况下,尽管具有HIV基因型敏感性模式,也可以进行表型分析。

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