Domer J E, Moser S A
Infect Immun. 1978 Apr;20(1):88-98. doi: 10.1128/iai.20.1.88-98.1978.
Attempts were made to isolate an antigen(s) from Candida albicans suitable for detecting hypersensitivity in a murine model of candidiasis. Using footpad reactivity in cutaneously infected animals as the assay, comparisons were made of two commercial extracts and cell wall and cytoplasmic preparations made in the laboratory. An extract of the cell wall, a glycoprotein (GP) removed with ethylenediamine, and an extract prepared from the membrane fraction of disrupted C. albicans blastospores proved most useful in demonstrating delayed hypersensitivity in the murine model. The activity of the GP fraction was considerably reduced by oxidation with periodate and was abrogated entirely by digestion with proteolytic enzymes. The extract from the membrane fraction was obtained by incubating the insoluble membrane fraction with phosphate-buffered saline, pH 7.4, at 50 degrees C, and the proteins in the extract were subsequently precipitated with ammonium sulfate to yield a test preparation that was approximately 75% protein and 25% carbohydrate. The precipitated extract was designated ppt-HEX. Footpad reactivity to ppt-HEX could be transferred with cells and not with serum if the cells were taken from animals at the appropriate time after sensitization. Since the membrane and GP fractions appear to elicit true delayed hypersensitivity reactions, further investigations into their specificity and biochemistry seem warranted.
人们试图从白色念珠菌中分离出一种抗原,以便在念珠菌病的小鼠模型中检测超敏反应。以皮肤感染动物的足垫反应性作为检测方法,对两种市售提取物以及实验室制备的细胞壁和细胞质制剂进行了比较。结果表明,细胞壁提取物、用乙二胺去除的一种糖蛋白(GP)以及由破碎的白色念珠菌芽生孢子的膜部分制备的提取物,在小鼠模型中最有助于证明迟发型超敏反应。GP部分的活性在用高碘酸盐氧化后显著降低,并用蛋白水解酶消化后则完全丧失。膜部分的提取物是通过将不溶性膜部分与pH 7.4的磷酸盐缓冲盐水在50℃下孵育获得的,提取物中的蛋白质随后用硫酸铵沉淀,得到一种测试制剂,其蛋白质含量约为75%,碳水化合物含量约为25%。沉淀的提取物被命名为ppt-HEX。如果在致敏后适当时间从动物体内获取细胞,足垫对ppt-HEX的反应性可以通过细胞传递,而不能通过血清传递。由于膜部分和GP部分似乎能引发真正的迟发型超敏反应,因此有必要对其特异性和生物化学进行进一步研究。