Targeting Alpha Toxin To Mitigate Its Lethal Toxicity in Ferret and Rabbit Models of Staphylococcus aureus Necrotizing Pneumonia.
Binh An DiepJamese J HilliardVien T M LeChristine TkaczykHoan N LeVuvi G TranRenee L RaoEtyene Castro DipEliane P Pereira-FranchiPaulyn ChaScott JacobsonRosemary BroomeLily I ChengWilliam WeissLaszlo ProkaiVien NguyenC Ken StoverBret R SellmanPublished in: Antimicrobial agents and chemotherapy (2017)
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.
Keyphrases
- staphylococcus aureus
- methicillin resistant staphylococcus aureus
- escherichia coli
- monoclonal antibody
- antimicrobial resistance
- respiratory failure
- healthcare
- community acquired pneumonia
- endothelial cells
- oxidative stress
- emergency department
- biofilm formation
- mental health
- small molecule
- extracorporeal membrane oxygenation
- mechanical ventilation
- drug delivery
- intensive care unit
- acute respiratory distress syndrome
- candida albicans
- smoking cessation
- induced pluripotent stem cells
- adverse drug