Immunotherapeutic strategies to combat staphylococcal infections

被引:51
作者
Ohlsen, Knut [1 ]
Lorenz, Udo [2 ]
机构
[1] Univ Wurzburg, Inst Mol Infect Biol, D-97080 Wurzburg, Germany
[2] Univ Clin Wurzburg, Ctr Operat Med, Dept Gen Visceral Vasc & Pediat Surg, Wurzburg, Germany
关键词
Staphylococcus aureus; MRSA; Vaccine; New targets; Immunotherapy; PANTON-VALENTINE LEUKOCIDIN; COMMUNITY-ASSOCIATED MRSA; HUMORAL IMMUNE-RESPONSE; CLUMPING FACTOR-A; CAPSULAR POLYSACCHARIDE; SURFACE-PROTEINS; VIRULENCE DETERMINANT; MONOCLONAL-ANTIBODIES; AUREUS INFECTIONS; NASAL CARRIERS;
D O I
10.1016/j.ijmm.2010.04.015
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Antibiotic-resistant staphylococci are the leading cause of nosocomial infections in many hospitals around the world. Meanwhile, methicillin-resistant Staphylococcus aureus (MRSA) spread also in the community where highly virulent strains infect healthy adults that have no predisposing risk factors. Although a few novel antibiotics have been recently introduced into clinical practice, the search for alternative strategies to efficiently combat staphylococcal infections is urgently demanded to decrease the enormous burden caused by pathogenic staphylococci. In particular, immunological strategies based on vaccine development or therapeutic antibodies may significantly enhance the efficiency of antistaphylococcal therapy. Most approaches are directed against surface components of staphylococci such as cell wall-linked adhesins, teichoic acids, capsule, the biofilm component PIA/PNAG, or soluble virulence determinants such as alpha-toxin, Panton-Valentine leukocidin, or superantigenic enterotoxins. Although 2 recent clinical trials have failed, several novel promising vaccines and therapeutic antibodies are currently in preclinical and clinical development. (C) 2010 Elsevier GmbH. All rights reserved.
引用
收藏
页码:402 / 410
页数:9
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