Literature DB >> 11451694

GT160-246, a toxin binding polymer for treatment of Clostridium difficile colitis.

C B Kurtz1, E P Cannon, A Brezzani, M Pitruzzello, C Dinardo, E Rinard, D W Acheson, R Fitzpatrick, P Kelly, K Shackett, A T Papoulis, P J Goddard, R H Barker, G P Palace, J D Klinger.   

Abstract

GT160-246, a high-molecular-weight soluble anionic polymer, was tested in vitro and in vivo for neutralization of Clostridium difficile toxin A and B activities. Five milligrams of GT160-246 per ml neutralized toxin-mediated inhibition of protein synthesis in Vero cells induced by 5 ng of toxin A per ml or 1.25 ng of toxin B per ml. In ligated rat ileal loops, 1 mg of GT160-246 neutralized fluid accumulation caused by 5 microg of toxin A. At doses as high as 80 mg/loop, cholestyramine provided incomplete neutralization of fluid accumulation caused by 5 microg of toxin A. GT160-246 protected 80% of the hamsters from mortality caused by infection with C. difficile, whereas cholestyramine protected only 10% of animals. Treatment of C. difficile-infected hamsters with metronidazole initially protected 100% of the hamsters from mortality, but upon removal of treatment, 80% of the hamsters had relapses and died. In contrast, removal of GT160-246 treatment did not result in disease relapse in the hamsters. GT160-246 showed no antimicrobial activity in tests with a panel of 16 aerobic bacteria and yeast and 22 anaerobic bacteria and did not interfere with the in vitro activities of most antibiotics. GT160-246 offers a novel, nonantimicrobial treatment of C. difficile disease in humans.

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Year:  2001        PMID: 11451694      PMCID: PMC90651          DOI: 10.1128/AAC.45.8.2340-2347.2001

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  25 in total

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Authors:  D M Lyerly; H C Krivan; T D Wilkins
Journal:  Clin Microbiol Rev       Date:  1988-01       Impact factor: 26.132

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Authors:  W L George; R D Rolfe; S M Finegold
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5.  Oligosaccharide sequences attached to an inert support (SYNSORB) as potential therapy for antibiotic-associated diarrhea and pseudomembranous colitis.

Authors:  L D Heerze; M A Kelm; J A Talbot; G D Armstrong
Journal:  J Infect Dis       Date:  1994-06       Impact factor: 5.226

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Journal:  Gastroenterol Clin North Am       Date:  1993-09       Impact factor: 3.806

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Authors:  N S Taylor; J G Bartlett
Journal:  J Infect Dis       Date:  1980-01       Impact factor: 5.226

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Authors:  S W Rothman; J E Brown; A Diecidue; D A Foret
Journal:  Infect Immun       Date:  1984-11       Impact factor: 3.441

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8.  A new formulation of tolevamer, a novel nonantibiotic polymer, is safe and well-tolerated in healthy volunteers: a randomized phase I trial.

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