Beno D W, Mathews H L
Department of Microbiology and Immunology, Stritch School of Medicine, Loyola University of Chicago, Maywood, IL 60153.
J Immunol Methods. 1993 Sep 15;164(2):155-64. doi: 10.1016/0022-1759(93)90308-t.
A rapid and reproducible assay has been developed to measure the capacity of lymphocytes to inhibit the growth of Candida albicans. Fungal growth inhibition was assessed optimally as the incorporation of [3H]uridine into preformed hyphae, following interaction of the hyphae with effector lymphocytes. The assay was sensitive to the detection of fungal growth inhibition by lymphocytes at low effector to target ratios and results correlated well with other methods for measurement of anti-C. albicans growth inhibition in vitro. Although the assay was developed for the measurement of lymphocyte mediated anti-fungal activity, other mammalian cell populations can be assayed for growth inhibition of C. albicans as well. The described assay utilizes the enzyme lyticase to reduce the surface binding of C. albicans. The use of this enzyme permits the efficient harvest of large numbers of experimental samples with a multiple automated sample harvester.
已开发出一种快速且可重复的检测方法,用于测量淋巴细胞抑制白色念珠菌生长的能力。在菌丝与效应淋巴细胞相互作用后,通过将[3H]尿苷掺入预先形成的菌丝中来最佳地评估真菌生长抑制情况。该检测方法在低效应细胞与靶细胞比例下对淋巴细胞介导的真菌生长抑制检测很敏感,并且结果与其他体外测量抗白色念珠菌生长抑制的方法相关性良好。尽管该检测方法是为测量淋巴细胞介导的抗真菌活性而开发的,但其他哺乳动物细胞群体也可用于检测白色念珠菌的生长抑制情况。所描述的检测方法利用溶菌酶来减少白色念珠菌的表面结合。使用这种酶可通过多通道自动样品收集器高效收集大量实验样品。