Fraser L B, Cater D B
Br J Exp Pathol. 1972 Apr;53(2):98-110.
C57 B1 mice were immunized against BP8 tumour cells emulsified in Freund's complete adjuvant. Spleens and lymph-nodes from the immunized animals were homogenized and crude preparations of mitochondria, microsomes and the soluble supernatant fraction were made by centrifugation. Injected into C3H mice, all 3 fractions were able to protect against fatal challenge with BP8 tumour cells, but only animals protected by the pellet fractions were able to reject a second challenge 40 days later. Protection by the soluble supernatant was not abolished by pretreatment with ribonuclease, and it was found that the active factor could be eluted from microsomes by treatment with EDTA. For comparison purposes some results of protecting C3H mice with similar extracts made from immunized C3H mice or guinea-pigs are included.
将C57 B1小鼠用弗氏完全佐剂乳化的BP8肿瘤细胞进行免疫。将免疫动物的脾脏和淋巴结匀浆,通过离心制备线粒体、微粒体和可溶性上清液部分的粗制品。注射到C3H小鼠体内后,所有这三个部分都能够保护小鼠免受BP8肿瘤细胞的致命攻击,但只有受沉淀部分保护的动物能够在40天后排斥第二次攻击。可溶性上清液的保护作用不会因用核糖核酸酶预处理而消除,并且发现活性因子可以通过用乙二胺四乙酸(EDTA)处理从微粒体中洗脱出来。为了进行比较,还包括了用免疫的C3H小鼠或豚鼠制备的类似提取物保护C3H小鼠的一些结果。