Shinomiya N, Tsuru S, Tsugita M, Takemura T, Katsura Y, Nomoto K
Department of Microbiology, National Defense Medical College, Saitama, Japan.
J Clin Lab Immunol. 1990 Oct;33(2):61-8.
In the present report, we compared activities of polymorphonuclear leukocytes (PMN) such as phagocytosis and bactericidal activity in vivo with those in vitro in sarcoma 180 (S 180)-bearing mice. Mice showed a remarkable leukocytosis and in increase in PMN fraction of peripheral blood leukocytes (PBL) after intraperitoneal injection of S 180 cells. Tumor-bearing mice infected with Escherichia coli (E. coli) intravenously and intraperitoneally showed an apparent delay in the clearance of bacteria compared to the non-tumor-bearing control mice. However, PBL of tumor-bearing mice showed a high phagocytic activity against beads and a high chemiluminescence (CL) activity. Dichlorofluorescein (DCFH) oxidation capacity of peripheral blood PMN in S 180-bearing mice after stimulation with phorbol myristate acetate (PMA) was about the same or a little stronger than that in control mice. On the contrary, serum and ascites of tumor-bearing mice strongly suppressed the phagocytic and bactericidal activities of casein-induced PMN against E. coli. During the early phase of E. coli infection, serum level of complement (C3) was not depressed in tumor-bearing hosts. From these results, it is concluded that leukocytosis and activation of functions of PMN in tumor-bearing mice were observed in vitro but they were not effective for the protection in the early phase of actual E. coli infection in vivo. The delay of in vivo clearance may be accounted for by a suppressive effect of serum components in tumor-bearing mice.
在本报告中,我们比较了荷肉瘤180(S 180)小鼠体内多形核白细胞(PMN)的吞噬作用和杀菌活性等活动与体外的情况。腹腔注射S 180细胞后,小鼠出现明显的白细胞增多,外周血白细胞(PBL)中PMN比例增加。与无肿瘤对照小鼠相比,经静脉和腹腔注射大肠杆菌(E. coli)的荷瘤小鼠清除细菌的时间明显延迟。然而,荷瘤小鼠的PBL对珠子表现出高吞噬活性和高化学发光(CL)活性。用佛波酯(PMA)刺激后,荷S 180小鼠外周血PMN的二氯荧光素(DCFH)氧化能力与对照小鼠大致相同或略强。相反,荷瘤小鼠的血清和腹水强烈抑制酪蛋白诱导的PMN对大肠杆菌的吞噬和杀菌活性。在大肠杆菌感染的早期阶段,荷瘤宿主的血清补体(C3)水平未降低。从这些结果可以得出结论,在体外观察到荷瘤小鼠白细胞增多和PMN功能激活,但它们在体内实际大肠杆菌感染的早期阶段对保护作用无效。体内清除延迟可能是由于荷瘤小鼠血清成分的抑制作用。