| Literature DB >> 28115346 |
Binh An Diep1, Jamese J Hilliard2, Vien T M Le3, Christine Tkaczyk2, Hoan N Le3, Vuvi G Tran3, Renee L Rao3, Etyene Castro Dip3, Eliane P Pereira-Franchi3, Paulyn Cha4, Scott Jacobson4, Rosemary Broome4, Lily I Cheng5, William Weiss6, Laszlo Prokai6, Vien Nguyen6, C Ken Stover2, Bret R Sellman7.
Abstract
The role broad-spectrum antibiotics play in the spread of antimicrobial resistance, coupled with their effect on the healthy microbiome, has led to advances in pathogen-specific approaches for the prevention or treatment of serious bacterial infections. One approach in clinical testing is passive immunization with a monoclonal antibody (MAb) targeting alpha toxin for the prevention or treatment of Staphylococcus aureus pneumonia. Passive immunization with the human anti-alpha toxin MAb, MEDI4893*, has been shown to improve disease outcome in murine S. aureus pneumonia models. The species specificity of some S. aureus toxins necessitates testing anti-S. aureus therapeutics in alternate species. We developed a necrotizing pneumonia model in ferrets and utilized an existing rabbit pneumonia model to characterize MEDI4893* protective activity in species other than mice. MEDI4893* prophylaxis reduced disease severity in ferret and rabbit pneumonia models against both community-associated methicillin-resistant S. aureus (MRSA) and hospital-associated MRSA strains. In addition, adjunctive treatment of MEDI4893* with either vancomycin or linezolid provided enhanced protection in rabbits relative to the antibiotics alone. These results confirm that MEDI4893 is a promising candidate for immunotherapy against S. aureus pneumonia.Entities:
Keywords: Staphylococcus aureus; alpha toxin; antibacterial; antibiotic; hemolysins; monoclonal antibodies
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Year: 2017 PMID: 28115346 PMCID: PMC5365647 DOI: 10.1128/AAC.02456-16
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191