Laird Veronika R, Plucinski Mateusz M, Venkatesan Meera, Rondini Kelsey A, Randrianarivelojosia Milijaona, Andriamananjara Mauricette N, Moonga Hawela, Ishengoma Deus S, Chidimatembue Arlindo, Dimbu Pedro Rafael, Adeothy Adicatou-Laï, Beavogui Abdoul Habib, Kariuki Simon, Nsobya Sam L, Uwimana Aline, Kahunu Gauthier Mesia, Assefa Ashenafi, Koita Ousmane A, Lucchi Naomi W, Souza Samaly S Svigel, Zhou Zhiyong, Moriarty Leah F, Halsey Eric S
Department of Epidemiology, Emory University, Atlanta, GA, USA.
Malaria Branch, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, US President's Malaria Initiative, Atlanta, GA, USA.
Malar J. 2025 Jun 12;24(1):186. doi: 10.1186/s12936-025-05248-2.
Plasmodium falciparum multidrug resistance transporter 1 (Pfmdr1) gene mutations are associated with altered response to artemisinin-based combination therapy (ACT), particularly the combinations containing the partner drugs lumefantrine and amodiaquine (i.e., artemether-lumefantrine [AL] and artesunate-amodiaquine [ASAQ]). Past studies of Pfmdr1 single nucleotide polymorphisms (SNPs) at codons 86, 184, and 1246 have shown different responses to AL and ASAQ.
To determine whether infection with parasites carrying specific Pfmdr1 SNPs leads to increased risk of recurrent parasitaemia (recrudescent or new infection), data from 3,915 samples from 16 therapeutic efficacy studies from 13 African countries between 2013 and 2019 were analysed.
Patients treated with AL and infected with parasites carrying Pfmdr1 N86 were at greater risk of recurrent infection than those whose parasites carried 86Y. After treatment with ASAQ, individuals infected with parasites that carried Pfmdr1 86Y were more likely to experience a recurrent infection.
These results support prior studies that suggested: (1) patients given AL and infected with parasites carrying N86 were more likely to experience a recurrent infection; (2) patients given ASAQ and infected with parasites carrying 86Y were more likely to experience a recurrent infection. These findings suggest that ACT and Pfmdr1 genotype may influence outcome after Plasmodium falciparum infection.
恶性疟原虫多药耐药转运蛋白1(Pfmdr1)基因突变与基于青蒿素的联合疗法(ACT)的反应改变有关,特别是含有辅助药物鲁美他尼和阿莫地喹的联合疗法(即蒿甲醚-鲁美他尼[AL]和青蒿琥酯-阿莫地喹[ASAQ])。过去对Pfmdr1第86、184和1246密码子单核苷酸多态性(SNP)的研究显示对AL和ASAQ有不同反应。
为确定感染携带特定Pfmdr1 SNP的寄生虫是否会导致复发性寄生虫血症(复发或新感染)风险增加,分析了2013年至2019年间来自13个非洲国家16项治疗效果研究的3915份样本数据。
接受AL治疗且感染携带Pfmdr1 N86寄生虫的患者比感染携带86Y寄生虫的患者有更高的复发感染风险。接受ASAQ治疗后,感染携带Pfmdr1 86Y寄生虫的个体更易出现复发感染。
这些结果支持先前的研究,表明:(1)接受AL治疗且感染携带N86寄生虫的患者更易出现复发感染;(2)接受ASAQ治疗且感染携带86Y寄生虫的患者更易出现复发感染。这些发现表明ACT和Pfmdr1基因型可能影响恶性疟原虫感染后的结局。