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Influence of lifelong cumulative HIV viremia on long-term recovery of CD4+ cell count and CD4+/CD8+ ratio among patients on combination antiretroviral therapy

机译:终生累积HIV病毒血症对联合抗逆转录病毒治疗的患者CD4 +细胞计数和CD4 + / CD8 +比率长期恢复的影响

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Objective: We explored the impact of lifelong cumulative HIV viremia on immuno-logical recovery during antiretroviral therapy, according to the timing of treatment initiation. Methods: We estimated lifelong cumulative HIV viremia in patients followed in the ANRS PRIMO cohort since primary infection, including 244 patients who started treatment during PHI and had at least one treatment interruption, and 218 patients who started treatment later but with no interruptions. The impact of cumulative viremia on current immunological status was analysed using linear and logistic regression models. Results: At the last visit on treatment, median CD4+ cell count was 645 cells/|xl in the early/intermittent treatment group (median time from infection 9.5 years, 4.8 years of continuous treatment since last resumption), and 654cells/|xl in the deferred/continuous treatment group (median time from infection 6.1 years, 3.0 years of continuous treatment). Only 36.1 and 39.8% of patients achieved a CD4+/CD8+ ratio of more than 1, respectively. Current CD4+ cell count was not associated with cumulative HIV viremia in either group. In contrast, patients with high cumulative HIV viremia (>66th percentile vs. <33rd percentile) were less likely to achieve a CD4+/CD8+ ratio of more than 1 (26.8 vs. 43.3%, P = 0.003), even after controlling for the baseline CD4+/CD8+ ratio, treatment duration, sex and age. Much higher CD4+ cell count and CD4+/CD8+ ratio were reached in early/continuous treatment, that is low viremia exposure group. Conclusion: Our results underline the critical need in early-treated patients to maintain adherence, in order to limit cumulative HIV viremia and optimize immunological recovery, notably the CD4+/CD8+ ratio.
机译:目的:我们根据治疗开始的时间,探讨了终身累积的HIV病毒血症对抗逆转录病毒治疗期间免疫学恢复的影响。方法:我们估计自初次感染以来在ANRS PRIMO队列中随访的患者终生累积HIV病毒血症,包括244例在PHI期间开始治疗且至少有一次治疗中断的患者,以及218例以后开始治疗但无中断的患者。使用线性和逻辑回归模型分析了累积病毒血症对当前免疫状态的影响。结果:在最后一次就诊时,早期/间断治疗组的CD4 +细胞计数中位数为645个细胞/ | xl(感染后的中位时间为9.5年,自上次复吸以来连续治疗的中位时间为4.8年),而在654 / cells中延迟/连续治疗组(感染后中位时间6.1年,连续治疗3.0年)。分别只有36.1和39.8%的患者CD4 + / CD8 +比值超过1。两组中当前的CD4 +细胞计数均与累积HIV病毒血症无关。相比之下,即使在控制了艾滋病毒/艾滋病毒/艾滋病毒/艾滋病毒/艾滋病病毒感染者之后,具有较高累积HIV病毒血症(> 66%与<33%)的患者也不太可能获得大于1的CD4 + / CD8 +比(26.8 vs. 43.3%,P = 0.003)。基线CD4 + / CD8 +比率,治疗时间,性别和年龄。早期/连续治疗即低病毒血症暴露组达到了更高的CD4 +细胞计数和CD4 + / CD8 +比率。结论:我们的结果强调了早期治疗的患者急需维持依从性,以限制累积的HIV病毒血症并优化免疫学恢复,尤其是CD4 + / CD8 +比率。

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