Takyi Abena, Soma Aboubakar, Przybylska Marianna, Harriss Eli, Barnes Karen I, Dahal Prabin, Guérin Philippe J, Stepniewska Kasia, Carrara Verena I
Department of Child Health, Korle Bu Teaching Hospital, Accra, Ghana.
Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Malar J. 2025 May 16;24(1):153. doi: 10.1186/s12936-025-05393-8.
Africa bears the highest double burden of HIV and malaria worldwide. In 2023, an estimated 25.9 million people were living with HIV (PLHIV), and 246 million malaria cases were diagnosed in Africa. Malaria patients co-infected with HIV are considered at a higher risk of failing malaria treatment, according to the World Health Organization (WHO) guidelines. This systematic literature review aims to assess the treatment outcomes following artemisinin-based combination therapy (ACT) in PLHIV.
The literature search was conducted up to April 2022 in the following databases: MEDLINE, EMBASE, Web of Science, Cochrane Central, WHO Global Index Medicus, Clinicaltrials.gov, and the WorldWide Antimalarial Resistance Network (WWARN) Clinical Trial Library. Studies describing any malaria treatment outcomes or anti-malarial drug exposure in PLHIV treated for uncomplicated Plasmodium falciparum malaria infection were eligible for inclusion.
A total of 26 articles describing 19 studies conducted between 2003 and 2017 in six countries were included in this review; it represented 2850 malaria episodes in PLHIV across various transmission settings. The most studied artemisinin-based combination was artemether-lumefantrine (in 16 studies). PLHIV were treated with various antiretroviral therapy (ART) regimens, namely efavirenz (EFV), nevirapine (NVP), atazanavir-ritonavir (ATVr), lopinavir-ritonavir (LPV/r), and/or on prophylaxis with trimethoprim-sulfamethoxazole (TS), or were untreated (in 3 studies). There was no evidence of an increased risk of recrudescence in PLHIV compared to those without HIV. When treated with artemether-lumefantrine, PLHIV receiving LPV/r had a lower risk of malaria recurrence compared to PLHIV on NVP-based or EFV-based ART, or those without HIV. LPV/r increased lumefantrine exposure and EFV-treated patients had a reduced exposure to both artemether and lumefantrine; NVP reduced artemether exposure only.
Limited data on ACT outcomes or drug exposure in PLHIV in Africa remains a reality to date, and the effect of antivirals appears inconsistent in the literature. Considering the heterogeneity in study designs, these review's findings support conducting an individual patient data meta-analysis to explore the impact of antiretroviral therapy on anti-malarial treatment.
The protocol for the original search was published on PROSPERO with registration number CRD42018089860.
非洲承受着全球最高的艾滋病病毒(HIV)和疟疾双重负担。2023年,非洲估计有2590万人感染HIV,共诊断出2.46亿例疟疾病例。根据世界卫生组织(WHO)的指南,合并感染HIV的疟疾患者被认为疟疾治疗失败的风险更高。本系统文献综述旨在评估HIV感染者接受以青蒿素为基础的联合疗法(ACT)后的治疗效果。
截至2022年4月,在以下数据库中进行文献检索:MEDLINE、EMBASE、科学网、Cochrane中心、WHO全球医学索引、Clinicaltrials.gov以及全球抗疟药耐药性网络(WWARN)临床试验库。描述在接受单纯性恶性疟原虫疟疾感染治疗的HIV感染者中任何疟疾治疗效果或抗疟药物暴露情况的研究均符合纳入标准。
本综述纳入了26篇文章,描述了2003年至2017年期间在六个国家进行的19项研究;这些研究代表了不同传播环境下2850例HIV感染者的疟疾病例。研究最多的以青蒿素为基础的联合用药是蒿甲醚-本芴醇(16项研究)。HIV感染者接受了各种抗逆转录病毒疗法(ART)方案,即依非韦伦(EFV)、奈韦拉平(NVP)、阿扎那韦-利托那韦(ATVr)、洛匹那韦-利托那韦(LPV/r),和/或接受甲氧苄啶-磺胺甲恶唑(TS)预防用药,或未接受治疗(3项研究)。没有证据表明与未感染HIV的人相比,HIV感染者复发风险增加。接受蒿甲醚-本芴醇治疗时,与接受基于NVP或EFV的ART的HIV感染者或未感染HIV的人相比,接受LPV/r的HIV感染者疟疾复发风险较低。LPV/r增加了本芴醇的暴露量,而接受EFV治疗的患者对蒿甲醚和本芴醇的暴露量均减少;NVP仅减少了蒿甲醚的暴露量。
迄今为止,非洲关于HIV感染者ACT治疗效果或药物暴露的数据仍然有限,抗病毒药物在文献中的效果似乎不一致。考虑到研究设计的异质性,本综述的结果支持进行个体患者数据荟萃分析,以探讨抗逆转录病毒疗法对抗疟治疗的影响。
原始检索方案已在PROSPERO上发表,注册号为CRD42018089860。