Open AccessThis article is
- freely available
Toxin-Specific Antibodies for the Treatment of Clostridium difficile: Current Status and Future Perspectives†
Institute for Biological Sciences, National Research Council of Canada, 100 Sussex Drive, Ottawa, Ontario, K1A 0R6, Canada
† This is NRC publication number 42534.
* Author to whom correspondence should be addressed.
Received: 26 March 2010; in revised form: 29 April 2010 / Accepted: 5 May 2010 / Published: 7 May 2010
Abstract: Therapeutic agents targeting bacterial virulence factors are gaining interest as non-antibiotic alternatives for the treatment of infectious diseases. Clostridium difficile is a Gram-positive pathogen that produces two primary virulence factors, enterotoxins A and B (TcdA and TcdB), which are responsible for Clostridium difficile-associated disease (CDAD) and are targets for CDAD therapy. Antibodies specific for TcdA and TcdB have been shown to effectively treat CDAD and prevent disease relapse in animal models and in humans. This review summarizes the various toxin-specific antibody formats and strategies under development, and discusses future directions for CDAD immunotherapy, including the use of engineered antibody fragments with robust biophysical properties for systemic and oral delivery.
Keywords: Clostridium difficile; Clostridium difficile-associated disease; toxin; antibody; single-domain antibody; neutralization; therapy
Article StatisticsClick here to load and display the download statistics.
Notes: Multiple requests from the same IP address are counted as one view.
Cite This Article
MDPI and ACS Style
Hussack, G.; Tanha, J. Toxin-Specific Antibodies for the Treatment of Clostridium difficile: Current Status and Future Perspectives. Toxins 2010, 2, 998-1018.
Hussack G, Tanha J. Toxin-Specific Antibodies for the Treatment of Clostridium difficile: Current Status and Future Perspectives. Toxins. 2010; 2(5):998-1018.
Hussack, Greg; Tanha, Jamshid. 2010. "Toxin-Specific Antibodies for the Treatment of Clostridium difficile: Current Status and Future Perspectives." Toxins 2, no. 5: 998-1018.