Targeting the host-pathogen interface for treatment of Staphylococcus aureus infection

被引:17
|
作者
Park, Bonggoo [1 ,2 ]
Liu, George Y. [1 ,2 ]
机构
[1] Cedars Sinai Med Ctr, Div Pediat Infect Dis, Los Angeles, CA 90048 USA
[2] Cedars Sinai Med Ctr, Immunobiol Res Inst, Los Angeles, CA 90048 USA
基金
美国国家卫生研究院;
关键词
S; aureus; MRSA; Virulence; Antibiotic resistance; Probiotics; Inflammation; PANTON-VALENTINE LEUKOCIDIN; COMMUNITY-ASSOCIATED MRSA; CHRONIC GRANULOMATOUS-DISEASE; VIRIDANS GROUP STREPTOCOCCI; FORMYL PEPTIDE RECEPTOR; INNATE IMMUNE-SYSTEM; BACTERIAL INTERFERENCE; IN-VIVO; ALPHA-TOXIN; NASAL CARRIAGE;
D O I
10.1007/s00281-011-0297-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent emergence of methicillin-resistant Staphylococcus aureus both within and outside healthcare settings has accelerated the use of once reserved last line antibiotics such as vancomycin. With increased use of antibiotics, there has been a rapid rise in the rate of resistance development to the anti-MRSA drugs. As the antibiotic pipeline becomes strained, alternative strategies are being sought for future treatment of S. aureus. Here, we review several novel antistaphylococcal strategies that, unlike conventional antibiotics, do not target essential gene products elaborated by the pathogen. The approaches seek instead to weaken the S. aureus defense by neutralizing its virulence factors or boosting host immunity. Other strategies target commensal bacteria that naturally colonize the human host to inhibit S. aureus colonization. Ultimately, the aim is to shift the balance between host defense and pathogen virulence in favor of inhibition of S. aureus pathogenic activities.
引用
收藏
页码:299 / 315
页数:17
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