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用抗志贺毒素(Stx)2人源化单克隆抗体TMA-15对产志贺毒素大肠杆菌致死性攻击的小鼠进行感染后治疗的效果。

Efficacy of postinfection treatment with anti-Shiga toxin (Stx) 2 humanized monoclonal antibody TMA-15 in mice lethally challenged with Stx-producing Escherichia coli.

作者信息

Yamagami S, Motoki M, Kimura T, Izumi H, Takeda T, Katsuura Y, Matsumoto Y

机构信息

Teijin Institute for Bio-Medical Research, Teijin Ltd., Tokyo 191-8512, Japan.

出版信息

J Infect Dis. 2001 Sep 15;184(6):738-42. doi: 10.1086/323082. Epub 2001 Aug 9.

Abstract

Infection with Shiga toxin (Stx)-producing Escherichia coli (STEC) causes hemorrhagic colitis and hemolytic uremic syndrome. TMA-15 is a humanized monoclonal antibody against Stx2, a major pathogenic factor. In a mouse infection model that used B2F1, a virulent STEC strain, the efficacy of TMA-15 was assessed when it was administered after bacterial and toxin exposure. In this model, a time-course analysis of the serum Stx2 level showed that the toxin was detectable from 24 h after infection. In an evaluation of the time-dependent efficacy, treatment with TMA-15 up to 24 h after infection ameliorated the lethal challenge, although treatment at 48 h showed no efficacy. To determine the effective dose, escalating doses were administered at 24 h after infection. The number of mice that survived after doses of 0, 0.25, 0.5, 1.0, and 2.0 mg/kg were 0/20, 11/20, 17/20, 20/20, and 20/20, respectively. These findings suggest that TMA-15 shows potential for prevention of severe complications associated with STEC infection.

摘要

感染产志贺毒素(Stx)的大肠杆菌(STEC)会导致出血性结肠炎和溶血尿毒综合征。TMA-15是一种针对主要致病因子Stx2的人源化单克隆抗体。在使用强毒STEC菌株B2F1的小鼠感染模型中,评估了细菌和毒素暴露后给予TMA-15的疗效。在该模型中,对血清Stx2水平的时间进程分析表明,感染后24小时即可检测到毒素。在评估时间依赖性疗效时,感染后24小时内用TMA-15治疗可减轻致死性攻击,尽管48小时治疗无效。为确定有效剂量,在感染后24小时给予递增剂量。0、0.25、0.5、1.0和2.0mg/kg剂量后存活的小鼠数量分别为0/20、11/20、17/20、20/20和20/20。这些发现表明,TMA-15在预防与STEC感染相关的严重并发症方面具有潜力。

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