Roberts J A, Kaack M B, Baskin G, Svenson S B
Department of Urology, Tulane University School of Medicine, New Orleans, Louisiana 70112.
Infect Immun. 1993 Dec;61(12):5214-8. doi: 10.1128/iai.61.12.5214-5218.1993.
Rhesus monkeys were vaccinated with a synthetic Escherichia coli serotype O8 oligosaccharide-protein conjugate. Using our experimental pyelonephritis monkey model, we tested whether such immunization was protective against the renal damage from inflammation following experimental infection with a P-fimbriated O-antigenically homologous E. coli strain. The vaccination did not significantly alter the duration of bacteriuria or interfere with the infection. However, the vaccine was efficient in renal protection, as vaccinated animals showed significantly less intratubular infiltration of neutrophils (P < 0.02) and the degree of renal scarring was also significantly less in these animals (P > 0.005) than in the control animals. Total kidney involvement in the vaccinated animals was 16.9%, compared with 32.5% in the control animals (P = 0.07).
恒河猴接种了一种合成的大肠杆菌O8血清型寡糖-蛋白共轭物。利用我们的实验性肾盂肾炎猴模型,我们测试了这种免疫接种是否能保护免受O抗原同源的菌毛P大肠杆菌菌株实验性感染后炎症引起的肾损伤。接种疫苗并没有显著改变菌尿持续时间或干扰感染。然而,该疫苗在肾脏保护方面是有效的,因为接种疫苗的动物肾小管内中性粒细胞浸润明显较少(P < 0.02),并且这些动物的肾瘢痕形成程度也明显低于对照动物(P > 0.005)。接种疫苗动物的肾脏总受累率为16.9%,而对照动物为32.5%(P = 0.07)。