van Dissel J T, Stikkelbroeck J J, Sluiter W, Leijh P C, van Furth R
J Immunol. 1986 Feb 1;136(3):1074-80.
The contribution of granulocytes to differences in the innate susceptibility of mouse strains to infection by Salmonella typhimurium was assessed on the basis of the size and composition of the inflammatory exudate after i.p. injection of bacteria and the intracellular killing of the bacteria by exudate peritoneal cells and blood granulocytes of resistant CBA and susceptible C57BL/10 mice. The increase in the numbers of both peritoneal granulocytes and macrophages 24 hr after i.p. injection of various numbers of live S. typhimurium was two to four times higher in C57BL/10 mice (p less than 0.05) than in CBA mice. However, despite the larger number of phagocytes in the inflammatory exudate, the numbers of viable S. typhimurium in the peritoneal cavity 24 hr after injection was higher (p less than 0.01) in C57BL/10 mice than in CBA mice. Because the proportion of noningested bacteria was similar in the two mouse strains (less than 30%), these findings indicate a difference in the rate of intracellular killing of the bacteria by exudate peritoneal cells (greater than 75% granulocytes) of the two mouse strains. Subsequent determination of the initial rate of intracellular killing (Kk) of S. typhimurium revealed that after phagocytosis of the bacteria in vivo, exudate peritoneal granulocytes (harvested 24 hr after i.p. injection of 10(3) live S. typhimurium) of CBA mice killed S. typhimurium twice as efficiently (Kk = 0.014 min-1; p less than 0.01) as exudate granulocytes of C57BL/10 mice (Kk = 0.008 min-1) did. Similarly, the initial rate of intracellular killing of the ingested S. typhimurium by blood granulocytes of CBA mice (Kk = 0.017 min-1) was two times higher (p less than 0.01) than that of C57BL/10 mice (Kk = 0.007 min-1). These findings may be specific for S. typhimurium, because L. monocytogenes were killed with equal efficiency by exudate granulocytes and blood granulocytes of these mouse strains (p greater than 0.20). The results of the present study are relevant with respect to the innate resistance of mice to S. typhimurium, particularly during the initial phase of infection when the inflammatory exudate contains predominantly granulocytes.
通过腹腔注射细菌后炎症渗出物的大小和组成,以及抗性CBA小鼠和易感C57BL/10小鼠的渗出腹膜细胞和血液粒细胞对细菌的细胞内杀伤作用,评估了粒细胞对小鼠品系对鼠伤寒沙门氏菌感染先天易感性差异的影响。腹腔注射不同数量的活鼠伤寒沙门氏菌24小时后,C57BL/10小鼠腹膜粒细胞和巨噬细胞数量的增加(p<0.05)比CBA小鼠高两到四倍。然而,尽管炎症渗出物中的吞噬细胞数量较多,但注射后24小时C57BL/10小鼠腹腔内活鼠伤寒沙门氏菌的数量(p<0.01)比CBA小鼠高。由于两种小鼠品系中未摄取细菌的比例相似(小于30%),这些发现表明两种小鼠品系的渗出腹膜细胞(大于75%为粒细胞)对细菌的细胞内杀伤率存在差异。随后对鼠伤寒沙门氏菌细胞内杀伤初始速率(Kk)的测定表明,在体内细菌被吞噬后,CBA小鼠的渗出腹膜粒细胞(腹腔注射10³ 活鼠伤寒沙门氏菌24小时后收获)杀伤鼠伤寒沙门氏菌的效率是C57BL/10小鼠渗出粒细胞(Kk = 0.008分钟⁻¹)的两倍(Kk = 0.014分钟⁻¹;p<0.01)。同样,CBA小鼠血液粒细胞对摄取的鼠伤寒沙门氏菌的细胞内杀伤初始速率(Kk = 0.017分钟⁻¹)比C57BL/10小鼠(Kk = 0.007分钟⁻¹)高两倍(p<0.01)。这些发现可能对鼠伤寒沙门氏菌具有特异性,因为这些小鼠品系的渗出粒细胞和血液粒细胞对单核细胞增生李斯特菌的杀伤效率相同(p>0.20)。本研究结果与小鼠对鼠伤寒沙门氏菌的先天抵抗力有关,特别是在感染初期,此时炎症渗出物主要含有粒细胞。