Kelly Christine, Gaskell Katherine M, Richardson Marty, Klein Nigel, Garner Paul, MacPherson Peter
Institute of Translation Medicine, University of Liverpool, Liverpool, United Kingdom.
Malawi Liverpool Wellcome Trust Clinical Research Program, Blantyre, Malawi.
PLoS One. 2016 Jun 10;11(6):e0156099. doi: 10.1371/journal.pone.0156099. eCollection 2016.
A discordant immune response (DIR) is a failure to satisfactorily increase CD4 counts on ART despite successful virological control. Literature on the clinical effects of DIR has not been systematically evaluated. We aimed to summarise the risk of mortality, AIDS and serious non-AIDS events associated with DIR with a systematic review.
The protocol is registered with the Centre for Review Dissemination, University of York (registration number CRD42014010821). Included studies investigated the effect of DIR on mortality, AIDS, or serious non-AIDS events in cohort studies or cohorts contained in arms of randomised controlled trials for adults aged 16 years or older. DIR was classified as a suboptimal CD4 count (as defined by the study) despite virological suppression following at least 6 months of ART. We systematically searched PubMed, Embase, and the Cochrane Library to December 2015. Risk of bias was assessed using the Cochrane tool for assessing risk of bias in cohort studies. Two authors applied inclusion criteria and one author extracted data. Risk ratios were calculated for each clinical outcome reported.
Of 20 studies that met the inclusion criteria, 14 different definitions of DIR were used. Risk ratios for mortality in patients with and without DIR ranged between 1.00 (95% CI 0.26 to 3.92) and 4.29 (95% CI 1.96 to 9.38) with the majority of studies reporting a 2 to 3 fold increase in risk.
DIR is associated with a marked increase in mortality in most studies but definitions vary widely. We propose a standardised definition to aid the development of management options for DIR.
不一致的免疫反应(DIR)是指尽管病毒学得到成功控制,但接受抗逆转录病毒治疗(ART)时CD4细胞计数未能令人满意地增加。关于DIR临床影响的文献尚未得到系统评估。我们旨在通过系统评价总结与DIR相关的死亡、艾滋病和严重非艾滋病事件的风险。
该方案已在约克大学评价传播中心注册(注册号CRD42014010821)。纳入的研究在队列研究或16岁及以上成年人随机对照试验各臂中的队列中,调查了DIR对死亡率、艾滋病或严重非艾滋病事件的影响。DIR被定义为在至少6个月的ART治疗后病毒学得到抑制但CD4细胞计数未达最佳水平(由研究定义)。我们系统检索了截至2015年12月的PubMed、Embase和Cochrane图书馆。使用Cochrane工具评估队列研究中的偏倚风险。两名作者应用纳入标准,一名作者提取数据。计算每个报告的临床结局的风险比。
在符合纳入标准的20项研究中,使用了14种不同的DIR定义。有DIR和无DIR患者的死亡风险比在1.00(95%CI 0.26至3.92)和4.29(95%CI 1.96至9.38)之间,大多数研究报告风险增加2至3倍。
在大多数研究中,DIR与死亡率显著增加相关,但定义差异很大。我们提出一个标准化定义,以帮助制定DIR的管理方案。