Vancomycin‐resistantent enterococci(VRE)に対する抗菌化学療法  リネゾリドを中心に

  • 柳原 克紀
    長崎大学医学部第二内科 長崎大学大学院医歯薬学総合研究科薬物治療学
  • 河野 茂
    長崎大学医学部第二内科 長崎大学大学院感染分子病態学

書誌事項

タイトル別名
  • Antimicrobial agents against vancomycin-resistant enterococci (Linezolid).
  • Resistant enterococci (Linezolid)mycin
  • リネゾリドを中心に

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抄録

Oxazolidinones are a new class of antimicrobials with a unique mechanism of action. This class of bacterial protein synthesis inhibitors functions by binding to the 50 S ribosomal subunit and preventing formation of a functional initiation complex in bacterial translation systems.Linezolid (LZD), an oxazolidinone anti-bacterial agent with a mechanism of action distinct from those of conventional antibacterial agents, was recently developed and its effectiveness against methicillin-resistant Staphylococcus aureus (MRSA) or vancomycin-insensitive S. aureus (VISA) highly anticipated. LZD has been approved as a new antibiotic against infections with gram-positive organisms by many countries, including the United States. Aclinical trial with LZD against MRSA infection hes been done in Japan.

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