Bitzan M, Moebius E, Ludwig K, Müller-Wiefel D E, Heesemann J, Karch H
Department of Pediatrics, University Hospital Hamburg-Eppendorf, Germany.
J Pediatr. 1991 Sep;119(3):380-5. doi: 10.1016/s0022-3476(05)82049-9.
Because the classic hemolytic-uremic syndrome has been etiologically linked to intestinal infections by Escherichia coli O157 and other verotoxin-producing E. coli (VTEC), we examined 22 consecutive children with acute hemolytic-uremic syndrome for the presence of VTEC, using microbiologic methods, and for a specific immune response to O157 lipopolysaccharide in acute-phase and follow-up sera, using the indirect hemagglutination assay and the immunoblot procedure. Of 22 children with enteropathic hemolytic-uremic syndrome, 15 (68%) had evidence of VTEC infection by culture of the pathogen or detection of free verotoxin in the feces, or both. Significantly elevated titers of short-lived agglutinins and IgM class antibodies against the O157 lipopolysaccharide were found in 20 (91%) of 22 patients, but not in two of three patients with non-O157 E. coli isolates or in healthy children or children with diarrhea caused by other enteric pathogens (p less than 0.01). The combined microbiologic and serologic procedures provided evidence for VTEC infection in all 22 patients. The high incidence of anti-O157 lipopolysaccharide antibodies in these patients indicates the predominance and the pathogenic potential of this serogroup. Both serologic techniques proved to be valuable tools to further characterize this form of hemolytic-uremic syndrome. Future studies on the induction of protective immunity seem warranted.
由于经典型溶血尿毒综合征在病因学上与大肠杆菌O157及其他产志贺毒素大肠杆菌(VTEC)引起的肠道感染有关,我们采用微生物学方法检查了22例连续性急性溶血尿毒综合征患儿是否存在VTEC,并采用间接血凝试验和免疫印迹法检测急性期及随访血清中对O157脂多糖的特异性免疫反应。在22例肠病性溶血尿毒综合征患儿中,15例(68%)通过病原体培养或粪便中游离志贺毒素检测或两者均检测到,有VTEC感染的证据。22例患者中有20例(91%)针对O157脂多糖的短寿命凝集素和IgM类抗体滴度显著升高,但在3例非O157大肠杆菌分离株患者中的2例、健康儿童或其他肠道病原体引起腹泻的儿童中未发现升高(P<0.01)。微生物学和血清学联合检测方法为所有22例患者的VTEC感染提供了证据。这些患者中抗O157脂多糖抗体的高发生率表明该血清群的优势地位及其致病潜力。两种血清学技术都被证明是进一步明确这种溶血尿毒综合征形式的有价值工具。未来关于诱导保护性免疫的研究似乎很有必要。