Characterization of a Protective Monoclonal AntibodyRecognizing Staphylococcus aureus MSCRAMM ProteinClumping FactorA

AE Hall, PJ Domanski, PR Patel… - Infection and …, 2003 - Am Soc Microbiol
AE Hall, PJ Domanski, PR Patel, JH Vernachio, PJ Syribeys, EL Gorovits, MA Johnson…
Infection and immunity, 2003Am Soc Microbiol
The Staphylococcus aureus MSCRAMM (microbial surface components recognizing
adhesive matrix molecules) protein clumping factor A (ClfA) has been shown to be a critical
virulence factor in several experimental models of infection. This report describes the
generation, characterization, and in vivo evaluation of a murine monoclonal antibody (MAb)
against ClfA. Flow cytometric analysis revealed that MAb 12-9 recognized ClfA protein
expressed by all of the clinical S. aureus strains obtained from a variety of sources. In assays …
Abstract
The Staphylococcus aureus MSCRAMM (microbial surface components recognizing adhesive matrix molecules) protein clumping factor A (ClfA) has been shown to be a critical virulence factor in several experimental models of infection. This report describes the generation, characterization, and in vivo evaluation of a murine monoclonal antibody (MAb) against ClfA. Flow cytometric analysis revealed that MAb 12-9 recognized ClfA protein expressed by all of the clinical S. aureus strains obtained from a variety of sources. In assays measuring whole-cell S. aureus binding to human fibrinogen, MAb 12-9 inhibited S. aureus binding by over 90% and displaced up to 35% of the previously adherent S. aureus bacteria. Furthermore, a single infusion of MAb 12-9 was protective against an intravenous challenge with a methicillin-resistant strain of S. aureus in a murine sepsis model (P< 0.0001). These data suggest that anti-ClfA MAb 12-9 should be further investigated as a novel immunotherapy for the treatment and prevention of life-threatening S. aureus infections.
American Society for Microbiology