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A Study of Methods for Producing Cell-free Tumour Antigen from BP8 Mouse Ascites Tumour

机译:从BP8小鼠腹水肿瘤中产生无细胞肿瘤抗原的方法研究

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摘要

One million lymph node cells (LNC) from C57 B1 mice immunized with BP8 cells plus Freund's complete adjuvant (FCA) protected C3H mice against fatal challenge with BP8 injected i.p. 20 hours later. The LNC of C57 B1 mice immunized with the supernatant from BP8 cells treated with lysolecithin (1·5 μg/106 cells) gave equally good protection. BP8 cells after treatment with lysolecithin equalled untreated BP8 cells in antigenic efficiency. Cell-free preparations made from BP8 cells with 3 molar KCl were of doubtful antigenic efficiency. The LNC from C57 B1 mice immunized with C3H liver and spleen tissue plus FCA gave no protection and LNC from non-immunized C57 B1 mice did not protect C3H mice against BP8 tumour.Centrifugation of the supernatants at 105,000 g indicated that the antigenic properties of the lysolecithin supernatant might be due to subcellular particles which were not found in the 3 molar KCl preparations.
机译:用BP8腹膜内注射BP8细胞和弗氏完全佐剂(FCA)免疫的C57 B1小鼠的一百万个淋巴结细胞(LNC)保护C3H小鼠免受致命性攻击。 20小时后。用溶血卵磷脂处理过的BP8细胞(1·5μg/ 10 6 细胞)的上清液免疫的C57 B1小鼠的LNC具有同样好的保护作用。溶血卵磷脂处理后的BP8细胞在抗原效率上等于未处理的BP8细胞。由具有3摩尔KCl的BP8细胞制成的无细胞制剂的抗原效率令人怀疑。用C3H肝,脾脏组织和FCA免疫的C57 B1小鼠的LNC没有提供保护,而未免疫的C57 B1小鼠的LNC则没有保护C3H小鼠免受BP8肿瘤的侵害.105,000 g的上清液的离心分离表明其抗原性溶血卵磷脂上清液可能是由于在3摩尔KCl制剂中未发现亚细胞颗粒所致。

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