Gal Isabella Ramella, Demarta-Gatsi Claudia, Fontinha Diana, Arez Francisca, Wicha Sebastian G, Rottmann Matthias, Nunes-Cabaço Helena, Blais Johanne, Jain Jay Prakash, Lakshminarayana Suresh B, Brito Catarina, Prudêncio Miguel, Alves Paula M, Spangenberg Thomas
iBET, Instituto de Biologia Experimental e Tecnológica, Apartado 12, 2780-901 Oeiras, Portugal.
Instituto de Tecnologia Química e Biológica António Xavier, Av. Republica, 2780-157 Oeiras, Portugal.
ACS Infect Dis. 2025 Jan 10;11(1):69-79. doi: 10.1021/acsinfecdis.4c00563. Epub 2024 Dec 10.
New antimalarial combination therapies with novel modes of action are required to counter the emergence and spread of drug resistance against existing therapeutics. Here, we present a study to evaluate the preventive activity of a combination of clinical antimalarial drug candidates, cabamiquine and ganaplacide, that have multistage activity against the liver and blood stages of infection. Cabamiquine (DDD107498, M5717) inhibits parasite protein synthesis, and ganaplacide (KAF156) inhibits protein trafficking, blocks the establishment of new permeation pathways, and causes endoplasmic reticulum expansion. The pharmacodynamic parameters of a combination of the two compounds were assessed employing a pharmacometrics approach in conjunction with checkerboard analysis. The study was performed on a previously established 3D infection platform based on human hepatic cell lines that sustain infection by rodent parasites. The efficacy of this drug combination was assessed against the liver stage of the . Our results show that the combination of both drugs at the tested concentrations does not interfere with the drugs respective mode of action or affect hepatocyte cell viability. The drug combination was fully effective in preventing the appearance of blood stage parasites when a systemic plasma C/EC ratio >2 for ganaplacide and >5 for cabamiquine was achieved. These findings demonstrate that chemoprevention using a combination of cabamiquine and ganaplacide has the potential to target the asymptomatic liver stage of infection and prevent the development of parasitemia.
需要具有新型作用模式的新型抗疟联合疗法来应对对现有疗法产生耐药性的出现和传播。在此,我们开展一项研究,以评估临床抗疟候选药物卡巴米喹和加纳普拉克的组合的预防活性,这两种药物对感染的肝脏和血液阶段具有多阶段活性。卡巴米喹(DDD107498,M5717)抑制寄生虫蛋白质合成,而加纳普拉克(KAF156)抑制蛋白质转运、阻止新渗透途径的建立并导致内质网扩张。采用药效学方法结合棋盘分析评估了两种化合物组合的药效学参数。该研究在基于人肝细胞系的先前建立的三维感染平台上进行,该平台可维持啮齿动物寄生虫的感染。评估了该药物组合对[具体寄生虫名称缺失]肝脏阶段的疗效。我们的结果表明,在测试浓度下,两种药物的组合不会干扰药物各自的作用模式,也不会影响肝细胞活力。当加纳普拉克的全身血浆C/EC比值>2且卡巴米喹>5时,该药物组合在预防血液阶段寄生虫出现方面完全有效。这些发现表明,使用卡巴米喹和加纳普拉克的组合进行化学预防有可能针对无症状的肝脏感染阶段并预防寄生虫血症的发展。