Scaffold vaccination for prevention of orthopedic device infection
Abstract
Staphylococcus aureus is the leading cause of global bacterial mortality. While S. aureus can cause a variety of diseases, orthopedic device infections are particularly challenging due to the need for additional surgeries with associated morbidity. Conventional vaccine technology has failed to prevent S. aureus orthopedic device infection in animal models and clinical trials. In this study, injectable scaffold vaccines are presented as a modality to augment host immunity and mitigate orthopedic device infection. These scaffold vaccines increased cytokine production, antigen-specific cell-mediated immune responses, and humoral responses. When loaded with a pool of antigens collected via an engineered human opsonin, these scaffold vaccines decreased the bacterial burden against methicillin-susceptible and methicillin-resistant S. aureus (MRSA) strains in a murine model of orthopedic device infection. Scaffold vaccination was ~100× more effective in decreasing S. aureus burden compared to prior published immunotherapy attempts in murine models of orthopedic device infection. Scaffold vaccination was also effective when using a monovalent protein-based antigen. Scaffold vaccination is an alternative strategy to facilitate more robust immunity in scenarios where conventional bolus vaccines have not been effective.
Article Details
Journal Info
Proceedings of the National Academy of Sciences
National Academy of Sciences
Authors (9)
Alexander M. Tatara
Department of Medicine, Division of Infectious Diseases, Massachusetts General Hospital
Shanda Lightbown
Harvard University Wyss Institute for Biologically Inspired Engineering
Shawn Kang
Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.
Wei-Hung Jung
Harvard University School of Engineering and Applied Sciences
Hamza Ijaz
Harvard University Wyss Institute for Biologically Inspired Engineering
Jean C. Lee
Brigham and Women’s Hospital, Department of Medicine, Division of Infectious Diseases
Sandra B. Nelson
Department of Medicine, Division of Infectious Diseases, Massachusetts General Hospital
Michael Super
Harvard University Wyss Institute for Biologically Inspired Engineering
David J. Mooney
Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.