Neutralizing Alpha-Toxin Accelerates Healing of Staphylococcus aureus-Infected Wounds in Nondiabetic and Diabetic Mice

• Published in: Antimicrobial agents and chemotherapy Vol. 62; no. 3
• Main Authors: Ortines, Roger V, Liu, Haiyun, Cheng, Lily I, Cohen, Taylor S, Lawlor, Heather, Gami, Abhishek, Wang, Yu, Dillen, Carly A, Archer, Nathan K, Miller, Robert J, Ashbaugh, Alyssa G, Pinsker, Bret L, Marchitto, Mark C, Tkaczyk, Christine, Stover, C Kendall, Sellman, Bret R, Miller, Lloyd S
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01-03-2018
• Subjects: Antibodies, Monoclonal; Antibodies, Neutralizing; Bacterial Toxins; Diabetes Mellitus, Experimental; Experimental Therapeutics; Hemolysin Proteins; Staphylococcal Skin Infections; Wound Healing; Wounds, Nonpenetrating; wound; wound healing; wound infection; alpha-toxin; macrophage; monocyte; neutrophil extracellular traps (NETs); hla; diabetes; neutrophil; Staphylococcus aureus
• ISSN: 0066-4804; 1098-6596
• DOI: 10.1128/aac.02288-17

wound infections delay healing and result in invasive complications such as osteomyelitis, especially in the setting of diabetic foot ulcers. In preclinical animal models of
skin infection, antibody neutralization of alpha-toxin (AT), an
-secreted pore-forming cytolytic toxin, reduces disease severity by inhibiting skin necrosis and restoring effective host immune responses. However, whether therapeutic neutralization of alpha-toxin is effective against
-infected wounds is unclear. Herein, the efficacy of prophylactic treatment with a human neutralizing anti-AT monoclonal antibody (MAb) was evaluated in an
skin wound infection model in nondiabetic and diabetic mice. In both nondiabetic and diabetic mice, anti-AT MAb treatment decreased wound size and bacterial burden and enhanced reepithelialization and wound resolution compared to control MAb treatment. Anti-AT MAb had distinctive effects on the host immune response, including decreased neutrophil and increased monocyte and macrophage infiltrates in nondiabetic mice and decreased neutrophil extracellular traps (NETs) in diabetic mice. Similar therapeutic efficacy was achieved with an active vaccine targeting AT. Taken together, neutralization of AT had a therapeutic effect against
-infected wounds in both nondiabetic and diabetic mice that was associated with differential effects on the host immune response.