Division of Dermatology, Department of Medicine, Montefiore Medical Center, Bronx, NY, USA.
Virulence. 2012 Jan-Feb;3(1):62-7. doi: 10.4161/viru.3.1.18816. Epub 2012 Jan 1.
Nitric oxide (NO) is a critical component of host defense against invading pathogens; however, its therapeutic utility is limited due to a lack of practical delivery systems. Recently, a NO-releasing nanoparticulate platform (NO-np) was shown to have in vitro broad-spectrum antimicrobial activity and in vivo pre-clinical efficacy in a dermal abscess model. To extend these findings, both topical (TP) and intralesional (IL) NO-np administration was evaluated in a MRSA intramuscular murine abscess model and compared with vancomycin. All treatment arms accelerated abscess clearance clinically, histologically, and by microbiological assays on both days 4 and 7 following infection. However, abscesses treated with NO-np via either route demonstrated a more substantial, statistically significant decrease in bacterial survival based on colony forming unit assays and histologically revealed less inflammatory cell infiltration and preserved muscular architecture. These data suggest that the NO-np may be an effective addition to our armament for deep soft tissue infections.
一氧化氮(NO)是宿主防御入侵病原体的关键组成部分;然而,由于缺乏实用的输送系统,其治疗用途受到限制。最近,一种释放一氧化氮的纳米颗粒平台(NO-np)在皮肤脓肿模型中显示出体外广谱抗菌活性和体内临床前疗效。为了扩展这些发现,在金黄色葡萄球菌肌肉脓肿小鼠模型中评估了局部(TP)和病灶内(IL)NO-np 给药,并与万古霉素进行了比较。所有治疗组在感染后第 4 天和第 7 天通过临床、组织学和微生物学检测均加速了脓肿清除。然而,通过任何途径用 NO-np 治疗的脓肿在基于集落形成单位检测的细菌存活方面表现出更大、具有统计学意义的降低,组织学显示炎症细胞浸润减少,肌肉结构得到保留。这些数据表明,NO-np 可能是深部软组织感染治疗的有效手段。