Druilhe P, Gentilini M
Med Trop (Mars). 1982 Jul-Aug;42(4):437-62.
Five years after Trager and Jensen fixed the requirements for a continuous culture of exo-erythrocytic stages in a semisynthetic medium, major advances have been realized. However all practical applications of this method have not yet been investigated. Its main interest is to offer the observation of the intraerythrocytic asexual multiplication and the beginning of the sexual cycle in monitored conditions, beyond the organism regulating processes, and with endless possibility to modify these conditions according to the necessities of the experiment. Compared with the previous use of expensive monkeys, this culture allows a study of P. falciparum in its natural host, cell, the human erythrocyte. It has been already applied for several investigations: - ultrastructure, metabolism, ADN and ARN sequencies of the parasite itself; - the relations between host and parasite (invasion of the erythrocyte by the merozoïte); - constitutional factors of resistance to malaria (hemoglobin S, C, E, deficiency in G6PD, elliptocytosis); - nutritional factors and immunologic defenses (antibodies, cytotoxic cells, ADCC...); - production of plasmodial antigens at the various erythrocytic stages; - chemotherapy (resistance to antimalarial drugs, screening of new drugs and study of their mode of action). The main disadvantages of Trager's and Jensen's method are for one part it concerns the sole erythrocytic stages and for the other part the parasite growth requires components of human origin (serum and erythrocytes). Human serum is hardly adapted to a standardization and appears as the main cause of variations observed in the in vitro proliferation of the parasite. Erythrocytes have a short survival and their metabolism is difficult to separate from that of the parasite. The minor disadvantages of the culture are: - a relative lack of reproductibility which raises difficulties for interpretation of inhibition tests either by antibodies or by antimalarial drugs; - a low output; - a rather expensive cost. Besides, adapting a strain to culture conditions probably induces clone selection (i.e.; loss of protuberances on the erythrocyte membrane). Paradoxically, the successful cultivation of erythrocytic stages raised a need to cultivate the other stages of parasite, that is to say, mainly, the exo-erythrocytic intra-hepatic stages and the sporogonic stages which take place in the mosquito. Somes valuable advances have been recently made in these two ways with animal parasites. The method of culture of P. falciparum has given to all laboratories, even to those out of the endemic area the most valuable opportunity to extend their investigations towards human malaria.
在特拉格和詹森确定了在半合成培养基中连续培养疟原虫红细胞外期的条件五年后,取得了重大进展。然而,这种方法的所有实际应用尚未得到研究。其主要意义在于能够在可控条件下观察疟原虫在红细胞内的无性繁殖以及有性周期的开始,不受生物体调节过程的限制,并且有无限可能根据实验需要改变这些条件。与以往使用昂贵的猴子相比,这种培养方法使得能够在其天然宿主细胞——人类红细胞中研究恶性疟原虫。它已被应用于多项研究:——寄生虫自身的超微结构、代谢、DNA和RNA序列;——宿主与寄生虫之间的关系(裂殖子侵入红细胞);——对疟疾的抗性构成因素(血红蛋白S、C、E、葡萄糖-6-磷酸脱氢酶缺乏症、椭圆形红细胞增多症);——营养因素和免疫防御(抗体、细胞毒性细胞、抗体依赖的细胞介导的细胞毒作用……);——疟原虫在不同红细胞阶段产生的抗原;——化疗(对抗疟药物的抗性、新药筛选及其作用方式的研究)。特拉格和詹森方法的主要缺点在于,一方面它仅涉及红细胞阶段,另一方面寄生虫生长需要人源成分(血清和红细胞)。人血清难以标准化,似乎是寄生虫体外增殖中观察到的变异的主要原因。红细胞存活时间短,其代谢难以与寄生虫的代谢区分开来。该培养方法的次要缺点包括:——相对缺乏可重复性,这给通过抗体或抗疟药物进行的抑制试验的解释带来困难;——产量低;——成本相当高。此外,使菌株适应培养条件可能会导致克隆选择(即红细胞膜上突起的丧失)。矛盾的是,红细胞阶段培养的成功引发了培养寄生虫其他阶段的需求,也就是说,主要是肝内红细胞外期和在蚊子体内发生的孢子生殖期。最近在这两个方面对动物寄生虫取得了一些有价值的进展。恶性疟原虫的培养方法为所有实验室,甚至是流行区以外的实验室提供了最宝贵的机会,将其研究扩展到人类疟疾。