Oligosaccharide Sequences Attached to an Inert Support (SYNSORB) as Potential Therapy for Antibiotic-Associated Diarrhea and Pseudomembranous Colitis
Toxin A produced by Clostridium difficile, the causative agent of pseudomembranous colitis and antibiotic-associated diarrhea, was shown to bind to synthetic oligosaccharide sequences attached to an inert support (SYNSORB). The oligosaccharide sequences that bind to toxin A were related to sequences...
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Published in: | The Journal of infectious diseases Vol. 169; no. 6; pp. 1291 - 1296 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Chicago, IL
The University of Chicago Press
01-06-1994
University of Chicago Press |
Subjects: | |
Online Access: | Get full text |
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Summary: | Toxin A produced by Clostridium difficile, the causative agent of pseudomembranous colitis and antibiotic-associated diarrhea, was shown to bind to synthetic oligosaccharide sequences attached to an inert support (SYNSORB). The oligosaccharide sequences that bind to toxin A were related to sequences previously identified as potential receptors for the toxin. Various SYNSORBs containing a variety of oligosaccharides were examined for their potential to neutralize toxin A activity from toxin-containing solutions as well as clinical stool samples from patients with either pseudomembranous colitisor antibiotic-associated diarrhea. The results from neutralization experiments suggest SYNSORB can effectively neutralize toxin A activity from stool samples and thus could serve as a potential therapy for C. difficile-associated diarrhea. |
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Bibliography: | istex:66C8FB45A46921863CE3E465CE7691E5C8D6E46F Reprints or correspondence: Dr. Louis D. Heerze, Dept. of Medical Microbiology and Infectious Diseases, 1-41 Medical Sciences Bldg., University of Alberta, Edmonton, Alberta. Canada T6G 2H7. ark:/67375/HXZ-RCKP9MGP-5 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0022-1899 1537-6613 |
DOI: | 10.1093/infdis/169.6.1291 |