The impact of transient combination antiretroviral treatment in early HIV infection on viral suppression and immunologic response in later treatment

N. Pantazis, G. Touloumi, L. Meyer, A. Olson, D. Costagliola, A. Kelleher, I. Lutsar, M. Chaix, M. Fisher, S. Moreno, K. Porter
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引用次数: 11

Abstract

Objective:Effects of transient combination antiretroviral treatment (cART) initiated during early HIV infection (EHI) remain unclear. We investigate whether this intervention affects viral suppression and CD4+ cell count increase following its reinitiation in chronic infection (CHI). Design:Longitudinal observational study. Methods:We identified adult patients from Concerted Action of Seroconversion to AIDS and Death in Europe who seroconverted after 1/1/2000, had a 12 months or less HIV test interval and initiated cART from naive. We classified individuals as ‘pretreated in EHI’ if treated within 6 months of seroconversion, interrupted for at least 12 weeks, and reinitiated during CHI. Statistical analysis was performed using survival analysis methods and mixed models. Results:Pretreated and initiated in CHI groups comprised 202 and 4263 individuals, with median follow-up after CHI treatment 4.5 and 3 years, respectively. Both groups had similar virologic response and relapse rates (P = 0.585 and P = 0.206) but pretreated individuals restarted treatment with higher baseline CD4+ cell count (∼80 cells/&mgr;l; P < 0.001) and retained significantly higher CD4+ cell count for more than 3 years after treatment (re)initiation. Assuming common baseline CD4+ cell count, differences in CD4+ cell count slopes were nonsignificant. Immunovirologic response to CHI treatment was not associated with timing or duration of the transient treatment. Conclusion:Although treatment interruptions are not recommended, stopping cART initiated in EHI does not seem to reduce the chance of a successful outcome of treatment in CHI.
早期HIV感染短暂联合抗逆转录病毒治疗对后期治疗中病毒抑制和免疫应答的影响
目的:早期HIV感染(EHI)时开始短暂联合抗逆转录病毒治疗(cART)的效果尚不清楚。我们研究这种干预是否影响病毒抑制和CD4+细胞计数在慢性感染(CHI)中重新启动后的增加。设计:纵向观察研究。方法:我们从欧洲血清转化为艾滋病和死亡的协调行动中找到了2000年1月1日之后血清转化的成年患者,他们有12个月或更短的HIV检测间隔,并且从幼稚开始进行cART。如果在血清转换后6个月内接受治疗,中断至少12周,并在CHI期间重新开始治疗,我们将个体分类为“EHI预处理”。采用生存分析方法和混合模型进行统计分析。结果:CHI治疗前和启动组分别有202人和4263人,CHI治疗后的中位随访时间分别为4.5年和3年。两组的病毒学反应和复发率相似(P = 0.585和P = 0.206),但预处理个体重新开始治疗时CD4+细胞计数基线较高(~ 80个细胞/&mgr; 1;P < 0.001),并且在治疗(重新)开始后的3年多时间里,CD4+细胞计数仍显著升高。假设基线CD4+细胞计数相同,CD4+细胞计数斜率差异不显著。对CHI治疗的免疫病毒学反应与短暂治疗的时间或持续时间无关。结论:虽然不建议中断治疗,但停止在EHI中启动的cART似乎并不会降低CHI治疗成功的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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