Stanisic Danielle I, McCarthy James S, Good Michael F
Institute for Glycomics, Griffith University, Southport, Queensland, Australia
School of Medicine, The University of Queensland, Herston, Queensland, Australia.
Infect Immun. 2017 Dec 19;86(1). doi: 10.1128/IAI.00479-17. Print 2018 Jan.
Controlled human malaria infection (CHMI) entails deliberate infection with malaria parasites either by mosquito bite or by direct injection of sporozoites or parasitized erythrocytes. When required, the resulting blood-stage infection is curtailed by the administration of antimalarial drugs. Inducing a malaria infection via inoculation with infected blood was first used as a treatment (malariotherapy) for neurosyphilis in Europe and the United States in the early 1900s. More recently, CHMI has been applied to the fields of malaria vaccine and drug development, where it is used to evaluate products in well-controlled early-phase proof-of-concept clinical studies, thus facilitating progression of only the most promising candidates for further evaluation in areas where malaria is endemic. Controlled infections have also been used to immunize against malaria infection. Historically, CHMI studies have been restricted by the need for access to insectaries housing infected mosquitoes or suitable malaria-infected individuals. Evaluation of vaccine and drug candidates has been constrained in these studies by the availability of a limited number of isolates. Recent advances have included cryopreservation of sporozoites, the manufacture of well-characterized and genetically distinct cultured malaria cell banks for blood-stage infection, and the availability of -specific reagents. These advances will help to accelerate malaria vaccine and drug development by making the reagents for CHMI more widely accessible and also enabling a more rigorous evaluation with multiple parasite strains and species. Here we discuss the different applications of CHMI, recent advances in the use of CHMI, and ongoing challenges for consideration.
人体疟疾感染控制(CHMI)是指通过蚊虫叮咬或直接注射子孢子或受疟原虫感染的红细胞,使人故意感染疟原虫。在需要时,可通过使用抗疟药物来控制由此产生的血液阶段感染。20世纪初,欧洲和美国首次将通过接种感染血液诱导疟疾感染用作治疗神经梅毒的方法(疟原虫疗法)。最近,CHMI已应用于疟疾疫苗和药物开发领域,用于在严格控制的早期概念验证临床研究中评估产品,从而仅推动最有前景的候选产品在疟疾流行地区进行进一步评估。受控感染也已用于预防疟疾感染。从历史上看,CHMI研究受到需要进入饲养感染蚊子的昆虫饲养室或合适的疟疾感染个体的限制。在这些研究中,疫苗和药物候选物的评估受到可用分离株数量有限的制约。最近的进展包括子孢子的冷冻保存、用于血液阶段感染的特征明确且基因不同的培养疟原虫细胞库的建立,以及特异性试剂的可用性。这些进展将有助于加速疟疾疫苗和药物的开发,使CHMI试剂更广泛地可用,并能够对多种寄生虫菌株和物种进行更严格的评估。在这里,我们讨论CHMI的不同应用、CHMI使用方面的最新进展以及需要考虑的持续挑战。