Forsyth C B, Mathews H L
Department of Microbiology and Immunology, Stritch School of Medicine, Loyola University of Chicago, Maywood, IL 60153.
J Immunol Methods. 1993 Sep 27;165(1):113-9. doi: 10.1016/0022-1759(93)90112-k.
A rapid and reproducible assay has been developed to measure the capacity of lymphocytes to bind to Candida albicans. Lymphocytes that bound to C. albicans were either the large granular lymphocyte cell line, YT, or interleukin-2 activated lymphocytes. Lymphocyte binding was assessed as the associated radioactivity of 51Cr-labeled lymphocytes with preformed hyphae. The assay was sensitive to detection of 0.6 lymphocytes/one hyphal form at one half maximal lymphocyte binding capacity. The assay correlated well with direct microscopic assessment of lymphocyte binding to C. albicans and provided quantitative radiometric data. Although the assay was developed for the assessment of lymphocyte adhesion to C. albicans, it can be used to measure binding of other mammalian cells (e.g., polymorphonuclear leukocytes) to this fungus. In addition, the assay may be used to identify molecules involved in the adhesion of lymphocytes and other mammalian cells to C. albicans.
已开发出一种快速且可重复的检测方法,用于测量淋巴细胞与白色念珠菌结合的能力。与白色念珠菌结合的淋巴细胞要么是大颗粒淋巴细胞系YT,要么是白细胞介素-2激活的淋巴细胞。淋巴细胞结合情况通过51Cr标记的淋巴细胞与预先形成的菌丝的相关放射性来评估。该检测方法在淋巴细胞最大结合能力的一半时,对检测每一个菌丝形态0.6个淋巴细胞很敏感。该检测方法与淋巴细胞与白色念珠菌结合的直接显微镜评估结果相关性良好,并提供定量放射性数据。尽管该检测方法是为评估淋巴细胞与白色念珠菌的黏附而开发的,但它可用于测量其他哺乳动物细胞(如多形核白细胞)与这种真菌的结合。此外,该检测方法可用于鉴定参与淋巴细胞和其他哺乳动物细胞与白色念珠菌黏附的分子。