Hanners Emily K, Benitez-Burke Jessica, Badowski Melissa E
Department of Pharmacy Practice, University of Illinois at Chicago, College of Pharmacy, Chicago, IL, USA.
Drugs Context. 2022 Mar 1;11. doi: 10.7573/dic.2021-8-13. eCollection 2022.
People living with HIV (PLWH) and receiving antiretroviral therapy (ART) have a goal of achieving and maintaining viral suppression; however, low-level viraemia (LLV) (HIV-RNA viral load levels of 50-999 copies/mL) persists in certain patients despite consistent medication adherence, lack of drug interactions and no genotypic resistance. This is a narrative review of the growing evidence of LLV in PLWH to determine risk factors and ART management strategies and to discuss the implications of LLV on the development of future virological failure.
A systematic, comprehensive literature search was completed in the English language using PubMed, Google Scholar and bibliography review to gather information about LLV in PLWH between July 2014 and June 2021. The following keywords were used as search terms: "low-level viremia", "HIV", "viral blip", "intensification", "genotyping", "adherence" and "resistance."
Of 66 studies examined, 39 were analysed and included in this review. All trials included were published between 2014 and 2021. Eleven studies assessed risk factors for LLV. Identified risk factors were low CD4 T cell nadir counts at baseline, higher baseline viral load measurements, medication non-adherence, non-nucleoside reverse transcriptase inhibitor use and others. Three studies assessed genotyping and concluded that the interpretation of both historical RNA genotype resistance testing and current proviral DNA genotype resistance testing in patients with LLV is appropriate. Seven studies were evaluated and determined that modifying or intensifying ART regimens resulted in decreased incidence of virological failure.
This compilation of reviewed data gives a framework for the management of PLWH with LLV. Currently, there are no clear or definitive treatment directions for LLV provided in guidelines. Complicating this topic further is the unclear and varying definitions of LLV. Future research is needed on this topic but patients presenting with LLV should have their medication adherence assessed, drug interactions checked and ART intensified, where appropriate.
感染人类免疫缺陷病毒(HIV)并接受抗逆转录病毒疗法(ART)的患者的目标是实现并维持病毒抑制;然而,尽管患者坚持规律服药、不存在药物相互作用且无基因型耐药,但部分患者仍存在低水平病毒血症(LLV)(HIV-RNA病毒载量水平为50 - 999拷贝/毫升)。本文是一篇叙述性综述,总结了关于HIV感染者中LLV的越来越多的证据,以确定风险因素和ART管理策略,并讨论LLV对未来病毒学失败发展的影响。
使用PubMed、谷歌学术搜索并进行文献综述,以英语完成了一项系统、全面的文献检索,收集2014年7月至2021年6月期间HIV感染者中LLV的相关信息。以下关键词用作检索词:“低水平病毒血症”、“HIV”、“病毒波动”、“强化治疗”、“基因分型”、“依从性”和“耐药性”。
在审查的66项研究中,39项进行了分析并纳入本综述。所有纳入的试验均发表于2014年至2021年之间。11项研究评估了LLV的风险因素。确定的风险因素包括基线时CD4 T细胞最低点计数低、基线病毒载量测量值较高、药物不依从、使用非核苷类逆转录酶抑制剂等。3项研究评估了基因分型,并得出结论,对LLV患者进行历史RNA基因型耐药性检测和当前前病毒DNA基因型耐药性检测的解读都是合适的。7项研究进行了评估并确定,调整或强化ART方案可降低病毒学失败的发生率。
本综述数据汇编为LLV的HIV感染者的管理提供了一个框架。目前,指南中没有针对LLV的明确或确定性治疗方向。使这个话题更加复杂的是LLV的定义不明确且各不相同。关于这个话题未来还需要进一步研究,但出现LLV的患者应评估其药物依从性,检查药物相互作用,并在适当情况下强化ART治疗。