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

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

  • J Infect Dis. 2001 Sep 15;184(6):738-42. doi: 10.1086/323082.
S Yamagami 1 M Motoki T Kimura H Izumi T Takeda Y Katsuura Y Matsumoto
Affiliations

Affiliation

  • 1 Teijin Institute for Bio-Medical Research, Teijin Ltd., Tokyo 191-8512, Japan. [email protected]
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.

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