Progress Toward a Staphylococcus aureus Vaccine

被引:140
作者
Daum, Robert S. [1 ]
Spellberg, Brad [2 ]
机构
[1] Univ Chicago, Dept Pediat, Med Ctr, Infect Dis Sect, Chicago, IL 60637 USA
[2] Harbor Univ Calif Los Angeles Med Ctr, Los Angeles Biomed Res Inst, Dept Med, Div Gen Internal Med, Los Angeles, CA USA
关键词
INTERCELLULAR-ADHESION; CONJUGATE VACCINE; PROTECTS MICE; INFECTIONS; EPIDEMIOLOGY; RESISTANCE; SPECIFICITY; CARRIAGE; DISEASE;
D O I
10.1093/cid/cir828
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
High attack rates and the ability of Staphylococcus aureus to develop resistance to all antibiotics in medical practice heightens the urgency for vaccine development. S. aureus causes many disease syndromes, including invasive disease, pneumonia, and skin and soft tissue infections. It remains unclear whether a single vaccine could protect against all of these. Vaccine composition is also challenging. Active immunization with conjugated types 5 and 8 capsular polysaccharides, an iron scavenging protein, isdB, and passive immunization against clumping factor A and lipoteichoic acid have all proven unsuccessful in clinical trials. Many experts advocate an approach using multiple antigens and have suggested that the right combination of antigens has not yet been identified. Others advocate that a successful vaccine will require antigens that work by multiple immunologic mechanisms. Targeting staphylococcal protein A and stimulating the T-helper 17 lymphocyte pathway have each received recent attention as alternative approaches to vaccination in addition to the more traditional identification of opsonophagocytic antibodies. Many questions remain as to how to successfully formulate a successful vaccine and to whom it should be deployed.
引用
收藏
页码:560 / 567
页数:8
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