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Virological suppression reduces clinical progression in patients with multiclass-resistant HIV type 1.

机译:病毒学抑制作用可降低1型多重耐药HIV患者的临床进展。

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摘要

The virological and immunological outcomes in patients carrying multiclass-resistant HIV-1, their predictors, and their impact on disease progression were investigated. Antiretroviral-experienced patients carrying at least one primary resistance mutation (IAS-USA 2006) to two to three classes of antiretroviral drugs were analyzed for achieving an HIV-1 RNA <50 copies/ml, a CD4 count increase of >200 cells/microl from baseline, and progression to an AIDS-defining event or death. Survival analysis was performed using the Kaplan-Meier estimates and predictors of different outcomes were analyzed using Cox's regression models. A total of 236 patients were identified. Of these 73% reached HIV-1 RNA <50 copies/ml. Higher genotypic sensitivity score of the salvage regimen, lower viral load, and more recent calendar year at genotyping were independently associated with virological response. Immunological response (58%) was predicted by a more recent calendar year, the achievement of an undetectable viral load, and higher CD4 counts at genotyping. Thirty-three patients showed clinical progression: achieving HIV-1 RNA <50 copies/ml predicted AIDS-free survival, independently from other significant cofactors. In individuals with multiclass-resistant HIV-1, virological suppression and immunological recovery are becoming more easily accessible with more recent therapies. The achievement of virological suppression is a strong predictor of reduced clinical progression.
机译:研究了携带多重耐药HIV-1的患者的病毒学和免疫学结果,其预测因子及其对疾病进展的影响。对经历过抗逆转录病毒治疗的,携带至少一种原发性耐药突变(IAS-USA 2006)至两到三类抗逆转录病毒药物的患者进行分析,以实现HIV-1 RNA <50拷贝/毫升,CD4计数增加> 200细胞/微升从基线到发展为定义艾滋病的事件或死亡。使用Kaplan-Meier估计进行生存分析,并使用Cox回归模型分析不同结果的预测因子。总共确定了236名患者。其中73%的HIV-1 RNA <50拷贝/ ml。挽救方案的较高的基因型敏感性评分,较低的病毒载量和较近的基因分型历年与病毒学应答独立相关。较新的日历年,无法检测到的病毒载量以及基因分型时较高的CD4计数可预测免疫反应(58%)。 33例患者显示出临床进展:独立于其他重要辅因子,HIV <1拷贝的HIV-1 RNA预测无艾滋病生存率。在具有多重耐药性HIV-1的个体中,采用最新的治疗方法变得更容易获得病毒学抑制和免疫学恢复。病毒抑制的实现是临床进展减少的有力预测指标。

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