Konadu E Y, Parke J C, Tran H T, Bryla D A, Robbins J B, Szu S C
National Institutes of Health, Bethesda, Maryland 20892-2720, USA.
J Infect Dis. 1998 Feb;177(2):383-7. doi: 10.1086/514203.
Escherichia coli O157 causes severe enteritis and the extraintestinal complication hemolytic-uremic syndrome. Serum IgG against the surface polysaccharide antigen, the O-specific polysaccharide of lipopolysaccharide (LPS), may confer protective immunity by lysing the inocula. In a phase 1 clinical study, three investigational vaccines were studied in 87 healthy adults. The vaccines were prepared by covalently binding E. coli O157 O-specific polysaccharide with Pseudomonas aeruginosa recombinant exoprotein A. No significant reactions were reported. Most volunteers (81%) responded with a > 4-fold increase in IgG LPS antibodies 1 week after vaccination; all volunteers responded with a > 4-fold rise at 4 weeks and this level was sustained for 26 weeks after injection. All three vaccines elicited high titers of serum bactericidal activity that roughly correlated with the serum IgG and IgM LPS antibody levels. A phase 2 study in young children is planned.
大肠杆菌O157可引发严重肠炎及肠外并发症溶血尿毒综合征。针对表面多糖抗原(脂多糖的O特异性多糖)的血清IgG,可能通过裂解接种物来赋予保护性免疫。在一项1期临床研究中,对87名健康成年人研究了三种研究性疫苗。这些疫苗是通过将大肠杆菌O157 O特异性多糖与铜绿假单胞菌重组外蛋白A共价结合制备而成。未报告有明显反应。大多数志愿者(81%)在接种疫苗1周后IgG LPS抗体增加了4倍以上;所有志愿者在4周时反应均为增加4倍以上,且该水平在注射后持续了26周。所有三种疫苗均引发了高滴度的血清杀菌活性,其大致与血清IgG和IgM LPS抗体水平相关。计划在幼儿中开展2期研究。