Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Int J Parasitol. 2012 Feb;42(2):155-60. doi: 10.1016/j.ijpara.2011.10.011. Epub 2011 Dec 27.
The establishment of a Plasmodium vivaxin vitro culture system is critical for the development of new vaccine, drugs and diagnostic tests. Although short-term cultures have been successfully set up, their reproducibility in laboratories without direct access to P. vivax-infected patients has been limited by the need for fresh parasite isolates. We explored the possibility of using parasite isolates and reticulocytes, both cryopreserved, to perform invasion and initiate short-term culture. Invasion results obtained with both cryopreserved isolates and reticulocytes were similar to those obtained with fresh samples. This method should be easily replicated in laboratories outside endemic areas and will substantially contribute to the development of a continuous P. vivax culture. In addition, this model could be used for testing vaccine candidates as well as for studying invasion-specific molecular mechanisms.
建立疟原虫(Plasmodium vivax)体外培养系统对于开发新型疫苗、药物和诊断测试至关重要。虽然已经成功建立了短期培养系统,但由于缺乏直接接触疟原虫感染患者的机会,需要新鲜的寄生虫分离物,这些培养系统在没有直接接触疟原虫感染患者的实验室中的可重复性受到限制。我们探索了使用冷冻保存的寄生虫分离物和网织红细胞进行入侵并启动短期培养的可能性。用冷冻保存的分离物和网织红细胞进行的入侵实验结果与用新鲜样本获得的结果相似。这种方法应该可以在非流行地区的实验室中轻松复制,这将极大地促进连续疟原虫培养的发展。此外,该模型可用于测试候选疫苗,以及研究入侵特异性分子机制。