Evron R
Infect Immun. 1980 Jun;28(3):963-71. doi: 10.1128/iai.28.3.963-971.1980.
The ability of sensitized mouse peritoneal macrophages to phagocytose and inhibit Candida albicans was studied in an in vitro system. Mice were sensitized to C. albicans by intraperitoneal infection with viable organisms or by intracutaneous injection of heat-inactivated cells in Freund complete adjuvant. Development of delayed hypersensitivity to C. albicans was evaluated by footpad tests with cytoplasmic and cell wall antigens as well as by macrophage migration inhibition by these antigens and by whole heat-inactivated cells. Inhibition of macrophage migration by heat-inactivated cells was significantly greater when the mice were sensitized by viable organisms. The macrophages from these mice were also larger and showed a greaer ability to inhibit germ tube production by phagocytosed yeasts. This suggests that macrophages may play a protective role in infection by C. albicans.
在体外系统中研究了致敏小鼠腹腔巨噬细胞吞噬和抑制白色念珠菌的能力。通过腹腔注射活的生物体或在弗氏完全佐剂中皮内注射热灭活细胞使小鼠对白色念珠菌致敏。通过用细胞质和细胞壁抗原进行足垫试验以及这些抗原和全热灭活细胞对巨噬细胞迁移的抑制来评估对白色念珠菌迟发型超敏反应的发展。当小鼠通过活的生物体致敏时,热灭活细胞对巨噬细胞迁移的抑制作用明显更大。这些小鼠的巨噬细胞也更大,并且显示出更强的抑制吞噬的酵母产生芽管的能力。这表明巨噬细胞可能在白色念珠菌感染中发挥保护作用。