Dormoi Jérôme, Amalvict Rémy, Gendrot Mathieu, Pradines Bruno
Unité Parasitologie et Entomologie, Département Microbiologie et Maladies Infectieuses, Institut de Recherche Biomédicale des Armées, 13005 Marseille, France.
Aix Marseille Univ, IRD, SSA, AP-HM, VITROME, 13005 Marseille, France.
Pharmaceutics. 2022 Sep 24;14(10):2031. doi: 10.3390/pharmaceutics14102031.
Untreated malaria can progress rapidly to severe forms (<24 h). Moreover, resistance to antimalarial drugs is a threat to global efforts to protect people from malaria. Given this, it is clear that new chemotherapy must be developed. We contribute new data about using methylene blue (MB) to cure malaria and cerebral malaria in a combined therapy with common antimalarial drugs, including mefloquine (MQ) and amodiaquine (AQ). A C57BL6/J mouse model was used in an experimental cerebral malaria model. Mice were infected with Plasmodium berghei ANKA on Day 0 (D0) and the treatment started on D3 (nearly 1% parasitaemia) with AQ, MQ or MB alone or in combination with AQ or MQ. AQ, MQ and MB alone were unable to prevent cerebral malaria as part of a late chemotherapy. MB-based combination therapies were efficient even if treatment began at a late stage. We found a significant difference in survival rate (p < 0.0001) between MBAQ and the untreated group, but also with the AQ (p = 0.0024) and MB groups (p < 0.0001). All the infected mice treated with MB in combination with AQ were protected from cerebral malaria. Partial protection was demonstrated with MB associated with MQ. In this group, a significant difference was found between MBMQ and the untreated group (p < 0.0001), MQ (p = 0.0079) and MB (p = 0.0039). MB associated with AQ would be a good candidate for preventing cerebral malaria.
未经治疗的疟疾可在短时间内(<24小时)迅速发展为重症形式。此外,疟原虫对抗疟药物的耐药性对全球疟疾防治工作构成威胁。鉴于此,显然必须研发新的化疗方法。我们提供了关于使用亚甲蓝(MB)与常用抗疟药物(包括甲氟喹(MQ)和阿莫地喹(AQ))联合治疗疟疾和脑型疟疾的新数据。在实验性脑型疟疾模型中使用C57BL6/J小鼠模型。小鼠于第0天(D0)感染伯氏疟原虫ANKA,并于第3天(寄生虫血症接近1%)开始单独使用AQ、MQ或MB,或与AQ或MQ联合治疗。单独使用AQ、MQ和MB作为晚期化疗的一部分无法预防脑型疟疾。基于MB的联合疗法即使在晚期开始治疗也有效。我们发现MBAQ组与未治疗组之间的生存率存在显著差异(p < 0.0001),与AQ组(p = 0.0024)和MB组(p < 0.0001)相比也有差异。所有接受MB与AQ联合治疗的感染小鼠均免受脑型疟疾侵害。MB与MQ联合显示出部分保护作用。在该组中,MBMQ组与未治疗组(p < 0.0001)、MQ组(p = 0.0079)和MB组(p = 0.0039)之间存在显著差异。MB与AQ联合可能是预防脑型疟疾的良好候选方案。