古巴多重耐药HIV病毒株感染患者中HIV-1对整合酶抑制剂的原发性和继发性耐药

Yanet Saavedra, L. rez, Vivian Cardell, M. lez, Jaime Pintos, J. Vila, C. Gómez, Elías Guilarte, Yudira Brito, Yoanna Morales, K. Fernández
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摘要

背景:古巴的研究表明,在接受治疗和未接受治疗的患者中,病毒耐药性水平很高。2017年,古巴引入了多替格拉韦作为一种救援疗法,并于2018年成为一线治疗方案。本研究的目的是确定古巴多重耐药患者中HIV-1对多替格拉韦的原发性和继发性耐药。方法:29例患者,其中23例未使用多替格拉韦治疗。扩增血浆病毒RNA,测序编码病毒整合酶的pol基因片段(3854-5981bp)。测定了29种病毒的病毒亚型。结果:所有患者均未发现多替格拉韦原发耐药突变。在治疗患者中发现频率较高的多态性位点为:112和119(均为73.9%)、125(69.5%)和201(78.2%)。在开始治疗后3个月和6个月,23名患者中有18名(78.2%)和23名患者中有14名(60.8%)分别实现了病毒学抑制。在这项研究之前接受多替格拉韦治疗的6例患者中,4例(66.7%)出现了对整合酶抑制剂的耐药。发现的亚型有:B(41%)、CRF19_cpx(24%)、CRF18_cpx和C(均为14%)和G(7%)。结论:未发现对DTG的原发性耐药,而在每日接受单剂量抗病毒药物治疗的患者中继发耐药较高。有必要深入研究一些多态性的作用,在某些亚型中更常见,以及它们对原发性耐药性的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary and secondary resistance of HIV-1 to integrase inhibitors in Cuban patients infected with multidrug-resistant HIV strains
Background: Cuban studies show high levels of viral resistance in treated and untreated patients. In 2017, dolutegravir was introduced as a rescue therapy in Cuba, and in 2018 as first-line regimens. The aim of this study was to determine the primary and secondary resistance of HIV-1 to dolutegravir in Cuban patients with multiple resistances. Methods: The sample consisted of 29 patients, of which 23 had not been treated with dolutegravir. The viral RNA isolated from plasma was amplified and the fragment of the pol gene encoding viral integrase (3854-5981bp) was sequenced. The viral subtype of the 29 viruses was determined. Results: No primary resistance mutations to dolutegravir were detected in any patient. The polymorphic positions found with greater frequency in the treated patients were: 112 and 119 (both with 73.9%), 125 (69.5%), and 201 (78.2%). Virological suppression was achieved in 18 out of 23 patients (78.2%) and in 14 out of 23 (60.8%) at three and six months after the start of treatment, respectively. Of the six patients who had received dolutegravir prior to this study, four (66.7%) developed resistance to integrase inhibitors. The subtypes found were: B (41%), CRF19_cpx (24%), CRF18_cpx and C (both 14%), and G (7%). Conclusion: Primary resistance to DTG was not detected, while secondary resistance was high in those patients who received a single daily dose of the antiviral. It is necessary to delve into the role of some polymorphisms, more frequent in certain subtypes, and their contribution to primary resistance.
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