金沙萨多来替韦治疗24周后艾滋病毒感染者的病毒学和分子特征

Berry I. Bongenya, Charlotte Tshinguta, Benoit O. Kabengele, Marie-Thérèse A. S. Sombo, Guy M. M. Bumoko, Mariano M. Lusakibanza, Gauthier K. Mesia, Erick N. Kamangu
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引用次数: 0

摘要

背景:M6的任命是至关重要的,因为它是护理发展的预后指标和继续抗逆转录病毒治疗的决策。目的:因此,本研究的目的是介绍在金沙萨接受抗逆转录病毒治疗6个月后接受Dolutegravir治疗的艾滋病毒感染者的病毒学和分子特征。方法:本研究是一项前瞻性队列研究的第6个月的横断面视图,以确定金沙萨基于Dolutegravir (DTG)的ART治疗6个月后HIV感染者(PLHIV)的病毒学和分子特征。从所有HIV患者身上抽取5毫升血液样本。生物学数据的收集在与纳入时相同的条件下进行。提取后,根据前面描述的方案进行定量Real-Time PCR测定样品中HIV RNA的数量。采用反转录PCR (RT-PCR)和巢式PCR扩增蛋白酶和逆转录酶感兴趣的区域进行测序。结果:中位VL值为2.92 log10 RNA拷贝/mL。17.75%的患者经历了一线治疗的重大失败。以A亚型为主,13例(20.98%);其次是CRF_02AG(16.13%)、C(14.52%)、D(9.68%)和K(6.45%)亚型。核苷酸逆转录酶抑制剂存在K65R(3例)、T69P/N(6例)、K70R(9例)和M184V(8例)突变。结论:经ART治疗6个月后,接受替诺福韦-拉米夫定-多替格拉韦治疗的HIV感染者中,59.67%的患者治疗成功,40.33%的患者治疗失败。亚型A在PLHIV人群中仍然占主导地位。拉米夫定和替诺福韦检测到耐药突变,而多路替韦未检测到耐药突变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Virological and Molecular Profile of People Living with HIV after 24 Weeks of Treatment with Dolutegravir in Kinshasa
Context: The appointment of the M6 is crucial because it is an indicator of the prognosis of the evolution of the care and the decision-making on the continuation of the AntiRetroViral Treatment. Objective: The objective of this study is therefore to present the virological and molecular profile of People Living with HIV under treatment with Dolutegravir 6 months after being put on ART in Kinshasa. Methods: The present study is a cross-sectional view at the sixth month of a prospective cohort to determine the virological and molecular profile of People Living with HIV (PLHIV) after 6 months of ART based on Dolutegravir (DTG) in Kinshasa. A sample of 5 mL of blood was taken from all HIV patients included. The collection of biological data was carried out under the same conditions as at inclusion. After extraction, Quantitative Real-Time PCR was carried out to determine the quantity of HIV RNA in the samples according to the protocols previously described. Reverse Transcription PCR (RT-PCR) and Nested PCR were carried out to amplify the regions of interest for Protease and Reverse Transcriptase for sequencing. Results: The median VL value was 2.92 log10 RNA copies/mL. With 17.75% of patients experiencing major failure of first-line treatment. Subtype A is dominant with 13 cases (20.98%); followed by CRF_02AG (16.13%), subtypes C (14.52%), D (9.68%) and K (6.45%). The K65R (3 cases), T69P/N (6 cases), K70R (9 cases) and M184V (8 cases) mutations were listed as existing mutations for Nucleotide Reverse Transcriptase Inhibitors. Conclusion: After 6 months of ART, 59.67% of People Living with HIV on Tenofovir-Lamivudine-Dolutegravir is in therapeutic success while 40.33% are in a state of treatment failure. Subtype A remains dominant in the population of PLHIV. Resistance mutations were detected for Lamivudine and Tenofovir, but none for Dolutegravir.
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