Efficacy of Postinfection Treatment with Anti-Shiga Toxin (Stx) 2 Humanized Monoclonal Antibody TMA-15 in Mice Lethally Challenged with Stx-Producing Escherichia coli.

Autor: Yamagani, Shunsuke, Motoki, Masamichi, Kimura, Tsuyoshi, Izumi, Hiroyuki, Takeda, Tae, Katsuura, Yasuhiro, Matsumoto, Yoh-ichi
Předmět:
Zdroj: Journal of Infectious Diseases; 9/15/2001, Vol. 184 Issue 6, p738, 5p
Abstrakt: 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. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index