Centre of Medical Research, Institute of Medical Research and Medicinal Plants Studies (IMPM), P.O. Box13033, Yaoundé, Cameroon.
Drugs for Neglected Diseases Initiative, Chemin Camille-Vidart 15, 1202, Geneva, Switzerland.
Parasitol Res. 2021 Dec;120(12):3939-3964. doi: 10.1007/s00436-021-07307-4. Epub 2021 Oct 13.
Twenty diseases are recognized as neglected tropical diseases (NTDs) by World Health Assembly resolutions, including human filarial diseases. The end of NTDs is embedded within the Sustainable Development Goals for 2030, under target 3.3. Onchocerciasis afflicts approximately 20.9 million people worldwide with > 90% of those infected residing in Africa. Control programs have made tremendous efforts in the management of onchocerciasis by mass drug administration and aerial larviciding; however, disease elimination is not yet achieved. In the new WHO roadmap, it is recognized that new drugs or drug regimens that kill or permanently sterilize adult filarial worms would significantly improve elimination timelines and accelerate the achievement of the program goal of disease elimination. Drug development is, however, handicapped by high attrition rates, and many promising molecules fail in preclinical development or in subsequent toxicological, safety and efficacy testing; thus, research and development (R&D) costs are, in aggregate, very high. Drug discovery and development for NTDs is largely driven by unmet medical needs put forward by the global health community; the area is underfunded and since no high return on investment is possible, there is no dedicated drug development pipeline for human filariasis. Repurposing existing drugs is one approach to filling the drug development pipeline for human filariasis. The high cost and slow pace of discovery and development of new drugs has led to the repurposing of "old" drugs, as this is more cost-effective and allows development timelines to be shortened. However, even if a drug is marketed for a human or veterinary indication, the safety margin and dosing regimen will need to be re-evaluated to determine the risk in humans. Drug repurposing is a promising approach to enlarging the pool of active molecules in the drug development pipeline. Another consideration when providing new treatment options is the use of combinations, which is not addressed in this review. We here summarize recent advances in the late preclinical or early clinical stage in the search for a potent macrofilaricide, including drugs against the nematode and against its endosymbiont, Wolbachia pipientis.
20 种疾病被世界卫生大会决议确认为被忽视的热带病(NTDs),包括人类丝虫病。NTDs 的终结被嵌入到 2030 年可持续发展目标中,目标 3.3 下。盘尾丝虫病影响全球约 2090 万人,其中 90%以上的感染者居住在非洲。控制规划在大规模药物管理和空中幼虫杀灭方面为盘尾丝虫病的管理做出了巨大努力;然而,疾病的消除尚未实现。在新的世卫组织路线图中,人们认识到,能够杀死或永久绝育成体丝虫的新药或药物方案将显著缩短消除时间表,并加速实现消除疾病的方案目标。然而,药物开发受到高淘汰率的阻碍,许多有前途的分子在临床前开发或随后的毒理学、安全性和疗效测试中失败;因此,研究和开发(R&D)成本加起来非常高。NTDs 的药物发现和开发主要由全球卫生界提出的未满足的医疗需求驱动;该领域资金不足,由于不可能有高投资回报,因此没有专门的人类丝虫病药物开发管道。重新利用现有药物是填补人类丝虫病药物开发管道的一种方法。新药物的发现和开发成本高、速度慢,导致了“旧”药物的重新利用,因为这更具成本效益,并允许缩短开发时间表。然而,即使一种药物已经上市用于人类或兽医适应症,也需要重新评估其安全性和剂量方案,以确定其在人类中的风险。药物再利用是扩大药物开发管道中有效分子库的一种很有前途的方法。在提供新的治疗选择时,另一个需要考虑的因素是联合用药,这在本综述中没有涉及。在这里,我们总结了在寻找有效的大丝虫杀剂方面,晚期临床前或早期临床阶段的最新进展,包括针对线虫和其共生菌沃尔巴克氏体的药物。