Clinic of Infectious Diseases, University of Modena and Reggio Emilia, Modena, Italy.
National Institute for Infectious Diseases, Rome, Italy.
Lancet HIV. 2015 Mar;2(3):e98-106. doi: 10.1016/S2352-3018(15)00006-5. Epub 2015 Feb 6.
In patients with HIV, immune reconstitution after antiretroviral therapy (ART) is often incomplete. We assessed the probability of patients reaching a CD4/CD8 ratio of 1 or more after the start of ART and its association with the onset of non-AIDS-defining events and death.
We did an analysis of the ICONA cohort, which recruited treatment-naive patients with HIV in Italy. We included participants in the cohort who started ART, reached an undetectable viral load (≤80 copies per mL), and had a CD4/CD8 ratio of less than 0·8 at the time of an undetectable viral load. We defined ratio normalisation in patients as two consecutive values of 1 or more. We used Kaplan-Meier curves to estimate the cumulative probability of ratio normalisation. We then used Poisson regression models to identify factors independently associated with normalisation and with progression to non-AIDS-defining events or death.
We included 3236 participants, enrolled between Jan 22, 1997, and Feb 25, 2013. At the start of ART, median CD4/CD8 ratio in our population was 0·39 (IQR 0·26-0·55). 458 (14%) patients reached a CD4/CD8 ratio of 1 or more; the estimated probability of normalisation was 4·4% (95% CI 3·7-5·2) by 1 year from baseline, 11·5% (10·2-13·0) by 2 years, and 29·4% (26·7-32·4) by 5 years. Factors associated with normalisation were high pre-ART CD4 cell counts, a high CD4/CD8 ratio at baseline, and negative cytomegalovirus serological findings. The incidence rate of non-AIDS-defining events for patients with a CD4/CD8 ratio of less than 0·30 (4·2 per 100 patient-years, 95% CI 3·4-5·3) was double that for those with a ratio of 0·30-0·45 (2·3, 2·1-2·5) or more than 0·45 (2·2, 1·7-2·9). A ratio of less than 0·30 was independently associated with an increased risk of non-AIDS-defining events or death compared with one of more than 0·45.
Few patients had normalised CD4/CD8 ratios, even though they had viral suppression. Low ratios were associated with increased risk of serious events and deaths. The CD4/CD8 ratio could be used by clinicians to identity patients at risk of non-AIDS-related events.
AbbVie, Bristol-Myers Squibb, Gilead, Janssen, Merck Sharp & Dohme, ViiV Italy.
在接受抗逆转录病毒疗法(ART)治疗的 HIV 感染者中,免疫重建通常并不完全。我们评估了开始 ART 后达到 CD4/CD8 比值 1 或更高的患者的可能性,以及其与非艾滋病定义性事件和死亡的发生之间的关系。
我们对 ICONA 队列进行了分析,该队列招募了意大利的 HIV 初治患者。我们纳入了在开始 ART 时达到不可检测的病毒载量(≤80 拷贝/毫升)且 CD4/CD8 比值小于 0.8 的患者。我们将患者的比值正常定义为两次连续的 1 或更高值。我们使用 Kaplan-Meier 曲线来估计比值正常化的累积概率。然后,我们使用泊松回归模型来确定与正常化以及向非艾滋病定义性事件或死亡进展相关的独立因素。
我们纳入了 3236 名参与者,他们于 1997 年 1 月 22 日至 2013 年 2 月 25 日期间入组。在开始 ART 时,我们人群中的中位 CD4/CD8 比值为 0.39(IQR 0.26-0.55)。458(14%)名患者达到了 CD4/CD8 比值 1 或更高;基线时,正常化的估计概率在 1 年内为 4.4%(95%CI 3.7-5.2),2 年内为 11.5%(10.2-13.0),5 年内为 29.4%(26.7-32.4)。与正常化相关的因素包括高基线前的 CD4 细胞计数、高基线 CD4/CD8 比值和巨细胞病毒血清学阴性结果。CD4/CD8 比值小于 0.30 的患者(每 100 名患者年 4.2 例,95%CI 3.4-5.3)的非艾滋病定义性事件发生率是 CD4/CD8 比值为 0.30-0.45(2.3,2.1-2.5)或大于 0.45(2.2,1.7-2.9)患者的两倍。与比值大于 0.45 相比,比值小于 0.30 与非艾滋病定义性事件或死亡风险增加独立相关。
尽管 HIV 感染者已经实现了病毒抑制,但只有少数患者的 CD4/CD8 比值正常化。较低的比值与严重事件和死亡风险增加相关。CD4/CD8 比值可用于临床医生识别有非艾滋病相关事件风险的患者。
艾伯维、百时美施贵宝、吉利德、杨森、默克夏普多姆、ViiV 意大利。