Mehlotra Rajeev K, Henry-Halldin Cara N, Zimmerman Peter A
Center for Global Health and Diseases, Case Western Reserve University, School of Medicine, Wolstein Research Building #4204, 2103 Cornell Road, Cleveland, OH 44106-7286, USA.
Pharmacogenomics. 2009 Mar;10(3):435-49. doi: 10.2217/14622416.10.3.435.
Drug resistance in malaria jeopardizes the most elementary objectives of malaria control--reducing suffering and eliminating mortality. An important, and so far the only known, mechanism of drug resistance appears to be polymorphisms in the malaria parasite genes. Efforts to circumvent antimalarial drug resistance now range from the use of combination therapies with existing agents to genomics-based studies directed toward discovering novel targets and agents. However, the potential contribution of host genetic/molecular factors, particularly those associated with antimalarial drug metabolism, remains largely unexplored. Our knowledge concerning the basic mechanisms involved in the pharmacokinetics of antimalarial drugs is fragmentary. In addition, the link between antimalarial drug pharmacokinetics and treatment outcomes is generally unclear. The purpose of this article is to provide general background information on antimalarial drug resistance and associated parasite genetic factors, and subsequently highlight the aforementioned unexplored and unclear areas, with a view to stimulate much needed further research.
疟疾耐药性危及疟疾控制的最基本目标——减轻痛苦和消除死亡。耐药性的一个重要且迄今为止唯一已知的机制似乎是疟原虫基因的多态性。目前,规避抗疟药物耐药性的努力范围广泛,从使用现有药物的联合疗法到旨在发现新靶点和新药物的基于基因组学的研究。然而,宿主遗传/分子因素的潜在贡献仍未得到充分探索,尤其是那些与抗疟药物代谢相关的因素。我们对抗疟药物药代动力学所涉及的基本机制的了解支离破碎。此外,抗疟药物药代动力学与治疗结果之间的联系通常也不明确。本文旨在提供有关抗疟药物耐药性及相关寄生虫遗传因素的一般背景信息,随后突出上述未探索和不明确的领域,以期激发急需的进一步研究。