Prevention of experimental Haemophilus ducreyi infection:: A randomized, controlled clinical trial

被引:28
作者
Thornton, AC
O'Mara, EM
Sorensen, SJ
Hiltke, TJ
Fortney, K
Katz, B
Shoup, RE
Hood, AF
Spinola, SM
机构
[1] Indiana Univ, Dept Med, Indianapolis, IN 46202 USA
[2] Indiana Univ, Dept Immunol & Microbiol, Indianapolis, IN 46202 USA
[3] Indiana Univ, Dept Pharm, Indianapolis, IN 46202 USA
[4] Indiana Univ, Dept Dermatol, Indianapolis, IN 46202 USA
[5] Indiana Univ, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
[6] BAS Analyt, W Lafayette, IN USA
关键词
D O I
10.1086/515320
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human subjects were infected with Haemophilus ducreyi All subjects developed papules and were randomized to treatment with a single dose of azithromycin (1g) or ciprofloxacin (500 mg). At weekly intervals, volunteers were reinoculated with H. ducreyi, and drug concentrations were measured in peripheral blood mononuclear cells (PBMC). When papules developed, the subjects were treated with antibiotics and dismissed from the study. Eight of the ciprofloxacin-treated subjects developed papules 1 week after the initial treatment, and the ninth subject developed disease 2 weeks after treatment. The 9 azithromycin-treated subjects developed papules 4-10 weeks (mean, 6.8) after the initial treatment (P < .001). Azithromycin was detected in PBMC for 3-6 weeks (mean, 4). Pre-and posttreatment lesions had histology typical of experimental chancroid or were culture positive. Azithromycin prevents experimental chancroid for nearly 2 months. These findings have implications for strategies to prevent chancroid.
引用
收藏
页码:1608 / 1613
页数:6
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