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Infect Immun, May 1998, p. 2018-2025, Vol. 66, No. 5
Ophidian Pharmaceuticals, Inc., Madison,
Wisconsin
Received 12 December 1997/Returned for modification 13 February
1998/Accepted 25 February 1998
Clostridium difficile causes antibiotic-associated
diarrhea and colitis in humans through the actions of toxin A and toxin B on the colonic mucosa. At present, broad-spectrum antibiotic drugs
are used to treat this disease, and patients suffer from high relapse
rates after termination of treatment. This study examined the role of
both toxins in pathogenesis and the ability of orally administered
avian antibodies against recombinant epitopes of toxin A and toxin B to
treat C. difficile-associated disease (CDAD). DNA fragments
representing the entire gene of each toxin were cloned, expressed, and
affinity purified. Hens were immunized with these purified
recombinant-protein fragments of toxin A and toxin B. Toxin-neutralizing antibodies fractionated from egg yolks were
evaluated by a toxin neutralization assay in Syrian hamsters. The
carboxy-terminal region of each toxin was most effective in generating
toxin-neutralizing antibodies. With a hamster infection model,
antibodies to both toxins A and B (CDAD antitoxin) were required to
prevent morbidity and mortality from infection. In contrast to
vancomycin, CDAD antitoxin prevented relapse and subsequent C. difficile reinfection in the hamsters. These results indicate that CDAD antitoxin may be effective in the treatment and management of
CDAD in humans.
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Antibodies to Recombinant Clostridium
difficile Toxins A and B Are an Effective Treatment and Prevent
Relapse of C. difficile-Associated Disease in a
Hamster Model of Infection
*
Corresponding author. Mailing address: Ophidian
Pharmaceuticals, Inc., 5445 East Cheryl Pkwy., Madison, WI 53711. Phone: (608) 271-0878. Fax: (608) 277-2395. E-mail: ophidian{at}ophd.com.
Present address: BioNebraska, Lincoln, NE 68524.
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