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PMID: 11451694 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

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

Antimicrobial agents and chemotherapy ·Vol. 45 ·No. 8 ·2001-08-00 ·Pages 2340-7

Kurtz CB, Cannon EP, Brezzani A, Pitruzzello M, Dinardo C, Rinard E, Acheson DW, Fitzpatrick R, Kelly P, Shackett K, Papoulis AT, Goddard PJ, Barker RH, Palace GP, Klinger JD

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.

MeSH Terms
Animals Bacterial Proteins/antagonists & inhibitors Bacterial Toxins/metabolism Chlorocebus aethiops Cholestyramine Resin/therapeutic use Clostridioides difficile/physiology Clostridium Infections/drug therapy,metabolism,microbiology Colitis/drug therapy,metabolism,microbiology Cricetinae Enterotoxins/metabolism Humans In Vitro Techniques Ions/metabolism,pharmacology,therapeutic use Lactams/pharmacology Male Metronidazole/therapeutic use Microbial Sensitivity Tests Polymers/metabolism,pharmacology,therapeutic use Rats Rats, Wistar Sulfonic Acids Survival Rate Vero Cells/microbiology
Chemicals
Bacterial Proteins Bacterial Toxins Enterotoxins Ions Lactams Polymers Sulfonic Acids tcdA protein, Clostridium difficile toxB protein, Clostridium difficile Cholestyramine Resin Metronidazole styrenesulfonic acid polymer
Authors & Affiliations
15 authors, click to expand affiliations / ORCID
Kurtz C B
GelTex Pharmaceuticals, Inc., Waltham, Massachusetts 02451, USA. [email protected]
Cannon E P
Brezzani A
Pitruzzello M
Dinardo C
Rinard E
Acheson D W
Fitzpatrick R
Kelly P
Shackett K
Papoulis A T
Goddard P J
Barker R H
Palace G P
Klinger J D
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Article Info
Journal
Antimicrobial agents and chemotherapy
Abbr.
Antimicrob Agents Chemother
ISSN
0066-4804
Published
2001-08-00
Pages
2340-7
Language
English
Region
United States
NLM ID
0315061
PMCID
PMC90651
Subset
IM
Analysis Services
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