Fançony Claudia, Fortes-Gabriel Elsa, Zage Félix, Alexiou Evangelia, Broumou Ioanna, Pernaute-Lau Leyre, Panzo Jorge, António Esperança J, Cristovão Mario S, Domingos José M, Sassoma Estevão, Kuatoko Fernando, Rosario Edite V N, Martins António, Färnert Anna, Bernardino Luis, de Sousa Tais N, Gil José Pedro
Centro de Investigação em Saúde de Angola, Instituto Nacional de Investigação em Saúde, Caxito, Angola.
Instituto Superior Técnico Militar, Luanda, Angola.
J Infect Dis. 2025 Jul 11;231(6):e1119-e1128. doi: 10.1093/infdis/jiaf155.
Decreased efficacy of artemether-lumefantrine, the globally most used antimalarial, has recently emerged in Africa.
An efficacy trial was carried out based on directly observed artemether-lumefantrine therapy at Bengo, Northern Angola. One-hundred Plasmodium falciparum uncomplicated malaria patients (2-10 years old) were enrolled, hospitalized for the treatment period, and followed up for 42 days. Polymerase chain reaction (PCR) correction was performed with pfmsp1/2 plus glurp, with analysis considering 2 or 3 coincident markers. Infections were tested by quantitative PCR (qPCR) for pfmdr1 copy number (pfmdr1×N), a potential P. falciparum marker of lumefantrine resistance previously identified in the region. In vitro clone mixtures were built and used to determine the relation between qPCR copy number scores and actual intrainfection quantitative fractions of pfmdr1×N.
We observed a significant posttreatment selection of gene amplification, suggesting a role in the parasite in vivo response to this drug. pfmdr1×2 qPCR scores of 1.3, 1.4, and 1.5 were determined to correspond to 15%, 25%, and 35% intrainfection rates. Patients carrying infections with a score ≥1.4 at baseline were linked to decreased artemether-lumefantrine day 42 efficacy (79% vs 97% single-copy pfmdr1). All infections were pfmdr1 N86 carriers and no pfk13 mutations were found.
Our study suggests pfmdr1×N as a marker of P. falciparum in vivo response to lumefantrine in Africa, while indicating patients carrying infections with a pretreatment pfmdr1×N score ≥1.4 before treatment are a group experiencing decreased artemether-lumefantrine performance.
全球使用最广泛的抗疟药物蒿甲醚-本芴醇的疗效近来在非洲有所下降。
在安哥拉北部的本戈,基于直接观察下的蒿甲醚-本芴醇疗法开展了一项疗效试验。招募了100名2至10岁的恶性疟原虫非重症疟疾患者,在治疗期间住院,并随访42天。使用pfmsp1/2加glurp进行聚合酶链反应(PCR)校正,分析时考虑2个或3个重合标记。通过定量PCR(qPCR)检测感染的pfmdr1拷贝数(pfmdr1×N),这是该地区先前确定的一个潜在的恶性疟原虫对本芴醇耐药性标记。构建体外克隆混合物并用于确定qPCR拷贝数分数与pfmdr1×N实际感染内定量分数之间的关系。
我们观察到治疗后基因扩增有明显的选择,提示其在寄生虫对该药物的体内反应中起作用。确定pfmdr1×2的qPCR分数为1.3、1.4和1.5分别对应感染内率为15%、25%和35%。基线时携带分数≥1.4感染的患者与蒿甲醚-本芴醇治疗第42天的疗效降低有关(单拷贝pfmdr1的患者为79%对97%)。所有感染均为pfmdr1 N86携带者,未发现pfk13突变。
我们的研究表明pfmdr1×N是非洲恶性疟原虫对本芴醇体内反应的一个标记,同时表明治疗前pfmdr1×N分数≥1.4的感染患者是蒿甲醚-本芴醇疗效降低的一组人群。