Boraschi D, Meltzer M S
J Immunol. 1979 Apr;122(4):1587-91.
Macrophages from A/J mice fail to develop tumoricidal activity after any of several in vivo or in vitro treatments that activate cells from C3H/HeN mice. Peritoneal macrophages from A/J mice treated i.p. with viable Mycobacterium bovis, strain BCG, killed Corynebacterium parvum, or pyran copolymer fail to develop in vitro tumoricidal activity; varying the numbers of macrophages from treated mice added to target cells, or the dose and time of treatment, or the treatment schedule of these in vivo activation stimuli did not evoke cytotoxic activity. Moreover, cytotoxic activity by macrophages from A/J mice was not observed with any of four target cell lines derived from three different mouse strains. In vitro treatment of peritoneal exudate macrophages from A/J mice with lymphokine-rich supernatants, bacterial endotoxins, or T cell mitogens was also ineffective; varying the numbers of treated macrophages added to target cells, the dose of in vitro activation stimuli, or the time of treatment did not evoke cytotoxic activity. Thus, A/J mice exhibit a profound defect in macrophage tumoricidal capacity to both in vivo and in vitro activation stimuli over a wide range of experimental conditions.
在几种能激活C3H/HeN小鼠细胞的体内或体外处理后,A/J小鼠的巨噬细胞无法产生杀肿瘤活性。用活的牛分枝杆菌卡介苗菌株经腹腔注射处理A/J小鼠后,其腹腔巨噬细胞对短小棒状杆菌或聚吡喃共聚物产生反应,但无法在体外产生杀肿瘤活性;改变从处理过的小鼠中添加到靶细胞的巨噬细胞数量、处理的剂量和时间,或这些体内激活刺激的处理方案,均无法引发细胞毒性活性。此外,来自A/J小鼠的巨噬细胞对源自三种不同小鼠品系的四种靶细胞系中的任何一种均未表现出细胞毒性活性。用富含淋巴因子的上清液、细菌内毒素或T细胞有丝分裂原对A/J小鼠的腹腔渗出巨噬细胞进行体外处理也无效;改变添加到靶细胞的处理过的巨噬细胞数量、体外激活刺激的剂量或处理时间,均无法引发细胞毒性活性。因此,在广泛的实验条件下,A/J小鼠在巨噬细胞杀肿瘤能力方面对体内和体外激活刺激均表现出严重缺陷。