A therapeutic agent with oriented carbohydrates for treatment of infections by Shiga toxin-producing <i>Escherichia coli</i> O157:H7

Kiyotaka Nishikawa(Jichi Medical University), Koji Matsuoka(Jichi Medical University), Eiji Kita(Jichi Medical University), Noriko Okabe(Jichi Medical University), Masashi Mizuguchi(Jichi Medical University), Kumiko Hino(Jichi Medical University), Shinobu Miyazawa(Jichi Medical University), Chisato Yamasaki(Jichi Medical University), Junken Aoki(Jichi Medical University), Sachio Takashima(Jichi Medical University), Yoshio Yamakawa(Jichi Medical University), Masahiro Nishijima(Jichi Medical University), Daiyo Terunuma(Jichi Medical University), Hiroyoshi Kuzuhara(Jichi Medical University), Yasuhiro Natori(Jichi Medical University)
Proceedings of the National Academy of Sciences
May 21, 2002
Cited by 198

Abstract

Infection with Shiga toxin (Stx)-producing Escherichia coli O157:H7, which causes diarrhea and hemorrhagic colitis in humans, often results in fatal systemic complications, such as neurological damage and hemolytic-uremic syndrome. Because Stx circulating in the blood is a major causative factor of these complications, the development of a Stx neutralizer that functions in the circulation holds promise as a viable therapy. Here we developed a series of carbosilane dendrimers, in which trisaccharides of globotriaosyl ceramide, a receptor for Stx, were variously oriented at their termini (referred to as SUPER TWIG), and identified a SUPER TWIG with six trisaccharides as a Stx neutralizer functioning in the circulation. This SUPER TWIG specifically bound to Stx with high affinity (K(d) = 1.1 x 10(-6) M) and inhibited the incorporation of the toxin into target cells. Intravenous administration of the SUPER TWIG along with Stx to mice substantially reduced the fatal brain damage and completely suppressed the lethal effect of Stx. Moreover, the SUPER TWIG protected mice from challenge with a fatal dose of E. coli O157:H7, even when administered after the establishment of the infection. The SUPER TWIG neutralized Stx in vivo by a mechanism in which the accumulation and immediate degradation of Stx by phagocytic macrophages present in the reticuloendothelial system were induced. Taken together, our findings indicate that this SUPER TWIG is therapeutic agent against infections by Stx-producing E. coli.


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