| Literature DB >> 24683195 |
Zhiyong Yang1, Diane Schmidt2, Weilong Liu2, Shan Li1, Lianfa Shi1, Jinliang Sheng1, Kevin Chen1, Hua Yu1, Jacqueline M Tremblay2, Xinhua Chen3, Kurt H Piepenbrink4, Eric J Sundberg5, Ciaran P Kelly3, Guang Bai6, Charles B Shoemaker2, Hanping Feng1.
Abstract
The incidence of Clostridium difficile infection (CDI) and associated mortality have increased rapidly worldwide in recent years. Therefore, it is critical to develop new therapies for CDI. In this study, we generated a novel, potently neutralizing, tetravalent, and bispecific antibody composed of 2 heavy-chain-only VH (VHH) binding domains against both TcdA and TcdB (designated "ABA") that reverses fulminant CDI in mice infected with an epidemic 027 strain after a single injection of the antibody. We demonstrated that ABA bound to both toxins simultaneously and displayed a significantly enhanced neutralizing activity both in vitro and in vivo. Additionally, ABA was able to broadly neutralize toxins from clinical C. difficile isolates that express both TcdA and TcdB but failed to neutralize the toxin from TcdA(-)TcdB(+) C. difficile strains. This study thus provides a rationale for the development of multivalent VHHs that target both toxins and are broadly neutralizing for treating severe CDI.Entities:
Keywords: Clostridium difficile; VHH; antibody; immunotherapy; toxins
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Year: 2014 PMID: 24683195 PMCID: PMC4192054 DOI: 10.1093/infdis/jiu196
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226