Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10965093 | Vaccine | 2015 | 4 Pages |
Abstract
Staphylococcus aureus is a cause of sepsis and meningitis in very-low-birth-weight (VLBW) infants. Clinical trials with S. aureus specific antibodies failed to protect VLBW neonates, which may be due to the immune evasive attributes of staphylococcal protein A (SpA). Here we show that mouse monoclonal antibody SpAKKAA-mAb 3F6, which neutralizes the immunoglobulin Fcγ-binding and B cell receptor crosslinking attributes of SpA, protects neonatal mice against S. aureus sepsis and raises protective immunity against subsequent staphylococcal infection. We developed a humanized SpAKKAA-mAb that protects neonatal mice against S. aureus sepsis and may therefore be subjected to clinical testing in VLBW neonates.
Keywords
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Immunology
Authors
Vilasack Thammavongsa, Sabine Rauch, Hwan Keun Kim, Dominique M. Missiakas, Olaf Schneewind,