Campbell G H, Mrema J E, O'Leary T R, Jost R C, Rieckmann K H
Bull World Health Organ. 1979;57 Suppl 1(Suppl):219-25.
An in vitro assay for measuring growth and reinvasion inhibition of Plasmodium falciparum was developed from a microculture system. Inhibition of growth was observed after parasites had been incubated with Aotus serum obtained from monkeys that had become immune to malaria after repeated exposure to P. falciparum. Immune Aotus serum (IAS), at concentrations as low as 1.25%, showed a marked inhibitory effect upon parasites cultured in 10% normal human serum (NHS). Growth was also inhibited when 5% of normal Aotus serum (NAS) was added to medium containing 10% of NHS. The inhibitory activity of NAS, but not of IAS, could be removed by lowering serum concentrations below 2.5% or by exposing the serum to 56 degrees C for 30 minutes. Further investigations with relatively synchronous microcultures showed that (3)H-hypoxanthine, a nucleic acid precursor, was incorporated preferentially into the more mature parasites of P. falciparum. Additional studies with the microculture system should elucidate the effects of immune serum on different asexual erythrocyte stages and, in general, facilitate the study of immune effector mechanisms in falciparum malaria.
一种用于测量恶性疟原虫生长和再侵袭抑制的体外试验是从微培养系统发展而来的。在寄生虫与从经反复暴露于恶性疟原虫后对疟疾产生免疫的猴子获得的夜猴血清一起孵育后,观察到了生长抑制。浓度低至1.25%的免疫夜猴血清(IAS)对在10%正常人血清(NHS)中培养的寄生虫显示出显著的抑制作用。当将5%的正常夜猴血清(NAS)添加到含有10%NHS的培养基中时,生长也受到抑制。通过将血清浓度降低到2.5%以下或使血清在56℃下暴露30分钟,可以去除NAS的抑制活性,但不能去除IAS的抑制活性。对相对同步的微培养物进行的进一步研究表明,核酸前体(3)H-次黄嘌呤优先掺入恶性疟原虫更成熟的寄生虫中。使用微培养系统进行的其他研究应阐明免疫血清对不同无性红细胞阶段的影响,并总体上促进对恶性疟免疫效应机制的研究。