塞内加尔引进多替格拉韦前HIV-1遗传多样性和预处理耐药调查

IF 1.7 Q4 INFECTIOUS DISEASES
Mengue Fall , Nafissatou Leye , Nicole Vidal , Fatou Niasse , Edmond Tchiakpe , Bambo Diakhaby , Mame Salane Thiam , Abou Abdallah Malick Diouara , Fabien Roch Niama , Safiatou Thiam , Coumba Toure-Kane , Halimatou Diop-Ndiaye
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引用次数: 0

摘要

本研究旨在记录塞内加尔therapy-naïve抗逆转录病毒患者的预处理耐药患病率,描述突变谱,并评估其对未来治疗的潜在影响。方法2017 - 2018年在全国35个地点采用干血点和全血样本进行预处理耐药调查。部分逆转录酶(RT)基因在HIV国家参比实验室使用法国国家获得性免疫缺陷综合征(艾滋病)和病毒性肝炎研究机构(ANRS)/AC11方法进行扩增和测序。采用校准种群耐药v8.1对监测耐药突变(SDRM)进行分析,按地理区域分组后评估SDRM的比例。结果共分析了来自不同患者的237份样本,131份(55.3%)成功扩增和测序。其中14个(10.7%)存在区域差异显著的SDRM。核苷类逆转录酶抑制剂(NRTI)的SDRM率以达喀尔地区最高(9.1%),其次是西南地区(5.3%)和东南部地区(4.2%)。对于非nrti (nnrti),东南部的发病率最高(20.8%),其次是达喀尔(13.6%),中西部(8.3%)和西南部(3.6%)。在nrti中,最常见的突变是M184V(3/6),对拉米夫定和恩曲他滨具有高水平耐药;nnrti中最常见的突变是K103N(11/12),对依非韦伦和奈韦拉平具有高水平耐药。值得注意的是,有4个序列同时含有NRTI和NNRTI的sdrm,这反映了一些患者的重叠耐药。与nrti相比,NNRTI耐药率较高与这些药物的遗传屏障较低是一致的,这可能促进了预处理耐药的出现。结论通过一项准全国性调查,塞内加尔的NNRTI耐药性处于中等水平,但存在地区差异。这些发现突出了塞内加尔以nnrti为基础的一线治疗方案的局限性,并支持向其他抗逆转录病毒治疗方案过渡,例如对新感染者和已接受治疗的患者进行以曲地韦为基础的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HIV-1 genetic diversity and pretreatment drug resistance survey prior to dolutegravir introduction in Senegal

Objectives

This study aimed to document the prevalence of pretreatment drug resistance in antiretroviral therapy-naïve patients in Senegal, describe mutation profiles, and evaluate their potential impact on future therapy.

Methods

A pretreatment drug resistance survey was carried out in 35 sites throughout the country between 2017 and 2018 using dried blood spots and whole blood samples. Amplification and sequencing were performed on the partial reverse transcriptase (RT) gene using the Agence Nationale de Recherches sur le Sida et les hépatitis virales (ANRS: French National Agency for Research on acquired immunodeficiency syndrome [AIDS] and Viral Hepatitis)/AC11 method at the HIV National Reference Laboratory. Surveillance drug resistance mutations (SDRM) were analyzed using the Calibrated Population Resistance v8.1, and the proportion of SDRM was evaluated after grouping sites by geographical areas.

Results

A total of 237 samples from different patients were analyzed, and 131 (55.3%) were successfully amplified and sequenced. Among these, 14 (10.7%) harbored SDRM with significant variability across regions. For nucleoside reverse transcriptase inhibitors (NRTI), the SDRM rate was highest in Dakar (9.1%), followed by the Southwest (5.3%) and the Southeast (4.2%). For non-NRTIs (NNRTIs), the highest rate was observed in the Southeast (20.8%), followed by Dakar (13.6%), the Midwest (8.3%), and the Southwest (3.6%). Among NRTIs, the most frequent mutation was M184V (3/6), conferring high-level resistance to lamivudine and emtricitabine, and K103N (11/12) among NNRTIs, conferring resistance to efavirenz and nevirapine. Notably, four sequences harbored SDRMs for both NRTI and NNRTI, reflecting overlapping resistance in some patients. The higher prevalence of NNRTI resistance is consistent with the lower genetic barrier of these drugs compared to NRTIs, which may facilitate the emergence of pretreatment drug resistance.

Conclusion

Through a quasi-national survey, an intermediate level of NNRTI resistance was observed, with regional disparities in Senegal. These findings highlight the limitations of NNRTI-based first-line regimens in Senegal and support the transition to other antiretroviral therapy regimens, such as dolutegravir-based therapy in newly infected individuals as well as in treated patients.
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IJID regions
IJID regions Infectious Diseases
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