现代抗逆转录病毒治疗时代CD4+ T淋巴细胞恢复:迈向定义免疫无应答的新门槛

IF 2 Q4 VIROLOGY
L. Taramasso, L. Labate, F. Briano, G. Brucci, S. Mora, S. Blanchi, M. Giacomini, M. Bassetti, A. di Biagio
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引用次数: 1

摘要

尽管现代抗逆转录病毒疗法(ART)在降低HIV病毒血症和控制病毒复制方面具有很高的疗效,但一些HIV感染者(PLWH)的CD4+ T细胞计数并没有恢复。方法为了评估不协调免疫应答的频率和预测因素,我们对324名antiretroviral-naïve PLWH进行了回顾性队列研究,这些患者在2008年至2018年期间开始一线抗逆转录病毒治疗,并在36个月的随访期间保持HIV RNA < 50拷贝/ml。当CD4+ T细胞计数与基线相比< 20% (INR20%),或36个月时< 500细胞/mm3 (INR500)或< 200细胞/mm3 (INR200)时,PLWH被定义为免疫无应答(INRs)。结果INR20%、INR500和INR200的患病率分别为12.5%、34.6%和1.5%。在对可能的混杂因素进行调整后,CD4最低点显示出与所有INR定义的显著关联,较低的值预测INR500 (aOR 0.98, 95% CI 0.98 - 0.99, p < 0.001)和INR200 (aOR 0.98, 95% CI 0.95-1.01, p = 0.096)。此外,较高的基线CD4/CD8比值与INR500 (OR 0.03, 95% CI 0.01-0.12, p < 0.001)和INR200 (OR 0.002, 95% CI 18-7-67.72, p = 0.255)的概率呈负相关。相比之下,INR20%的CD4最低点和CD4/CD8比值高于其他inr,表明具有这种定义的异质性人群。本研究强调了INR200在当代ART时代是如何变得罕见的,大约三分之一的PLWH符合INR500的标准。与以前的定义INR200和INR20%相比,超过500 CD4/mm3的阈值可能是免疫反应的适当定义。在CD4计数和CD4/CD8比值开始下降之前,早期诊断和快速治疗是实现最佳免疫反应的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CD4+ T lymphocyte recovery in the modern antiretroviral therapy era: Toward a new threshold for defining immunological non-responders
Introduction Despite the high level of efficacy of modern antiretroviral therapy (ART) in reducing HIV viremia and the control of viral replication, some people living with HIV (PLWH) do not recover their CD4+ T cell count. Methods To evaluate the frequency and predictive factors of discordant immune responses, we performed a retrospective cohort study of 324 antiretroviral-naïve PLWH who initiated first-line ART between 2008 and 2018 and maintained HIV RNA < 50 copies/ml during 36 months of follow-up. PLWH were defined as immunological non-responders (INRs) when CD4+ T cell count was < 20% compared with baseline (INR20%), or < 500 cells/mm3 (INR500) or < 200 cells/mm3 (INR200) at 36 months. Results The prevalence of INR20%, INR500, and INR200 was 12.5%, 34.6%, and 1.5%, respectively. After adjustment for possible confounders, CD4 nadir showed a significant association with all INR definitions, with lower values predicting INR500 (aOR 0.98, 95% CI 0.98–0.99, p < 0.001) and INR200 (aOR 0.98, 95% CI 0.95–1.01, p = 0.096). Moreover, a higher baseline CD4/CD8 ratio was inversely related to the probability of being INR500 (OR 0.03, 95% CI 0.01–0.12, p < 0.001) and INR200 (OR 0.002, 95% CI 18–7–67.72, p = 0.255). By contrast, INR20% had a higher CD4 nadir and CD4/CD8 ratio than other INRs, suggesting the identification of an heterogenous population with such definition. Discussion The present study highlights how INR200 has become rare in the contemporary ART era, and about one-third of PLWH meet the criteria for INR500. Overcoming the threshold of 500 CD4/mm3 could be an appropriate definition of immune response, in contrast with the older definitions of INR200 and INR20%. Early diagnosis and rapid treatment initiation, before CD4 counts and the CD4/CD8 ratio begin to decline, are critical for achieving an optimal immune response.
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