Redd H, Christensen R D, Fischer G W
Division of Human Development and Aging, University of Utah School of Medicine, Salt Lake City 81432.
J Infect Dis. 1988 Apr;157(4):705-12. doi: 10.1093/infdis/157.4.705.
Marked neutropenia, complete depletion of the neutrophil storage pool, and death within 48 h were observed in newborn rats intrapulmonically inoculated with 10(5) type III group B streptococci (GBS). Intraperitoneal administration of 225 mg of intravenous human immune globulin (IVIG) immediately after intrapulmonic inoculation of GBS significantly lessened the degree of neutropenia and prevented depletion of the neutrophil storage pool and death. No effect of IVIG on neutrophil production was observed in vitro, in cultures of granulocytic progenitor cells, or in vivo, as assessed by quantifying circulating and storage pools in normal neonatal rats injected with IVIG. IVIG, however, markedly hastened release of neutrophils from the reserves into the blood and hastened the arrival of neutrophils at the site of the bacterial injection (the right lung). Specific antibody to GBS, as opposed to a nonspecific IgG effect, appeared to be responsible for the improvements in neutrophils kinetics and for survival of the animals.
在经肺内接种10(5)型B族链球菌(GBS)的新生大鼠中,观察到明显的中性粒细胞减少、中性粒细胞储存池完全耗竭以及在48小时内死亡。在肺内接种GBS后立即腹腔注射225mg静脉用人免疫球蛋白(IVIG),可显著减轻中性粒细胞减少的程度,并防止中性粒细胞储存池耗竭和死亡。通过对注射IVIG的正常新生大鼠的循环池和储存池进行定量评估,未观察到IVIG在体外、粒细胞祖细胞培养物中或体内对中性粒细胞生成有影响。然而,IVIG显著加速了中性粒细胞从储备中释放到血液中,并加速了中性粒细胞到达细菌注射部位(右肺)。与非特异性IgG效应相反,GBS特异性抗体似乎是中性粒细胞动力学改善和动物存活的原因。