Evaluation of serotypes 5 and 8 capsular polysaccharides in protection against Staphylococcus aureus in murine models of infection

Staphylococcus aureus is the leading cause of nosocomial and community-acquired infections, including soft tissue and skin infections and bacteremia. However, efforts to develop an effective vaccine against S. aureus infections have not been successful. We evaluated serotypes 5 and 8 capsule polysac...

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מידע ביבליוגרפי
Main Authors: Brian L. Cheng, Travis B. Nielsen, Paul Pantapalangkoor, Fan Zhao, Jean C. Lee, Christopher P. Montgomery, Brian Luna, Brad Spellberg, Robert S. Daum
פורמט: Article
שפה:English
יצא לאור: Taylor & Francis Group 2017-07-01
סדרה:Human Vaccines & Immunotherapeutics
נושאים:
גישה מקוונת:http://dx.doi.org/10.1080/21645515.2017.1304334
תיאור
סיכום:Staphylococcus aureus is the leading cause of nosocomial and community-acquired infections, including soft tissue and skin infections and bacteremia. However, efforts to develop an effective vaccine against S. aureus infections have not been successful. We evaluated serotypes 5 and 8 capsule polysaccharides (CP) CRM197 conjugates as vaccine candidates in murine models of bacteremia, lethal sepsis, and skin infection. The conjugate vaccines elicited a good antibody response, and active immunization of CP5-CRM or CP8-CRM conjugates protected against staphylococcal bacteremia. In the skin infection model, CP8-CRM but not CP5-CRM protected against dermonecrosis, and CP8-CRM immunization significantly decreased the bacterial burden in the lesion. However, neither CP5-CRM nor CP8-CRM protected against mortality in the lethal sepsis model. The results indicate the capsular vaccines elicit protection against some, but not all, aspects of staphylococcal infection.
ISSN:2164-5515
2164-554X