Efficacy of an Immune Modulator in Experimental <emph>Chlamydia trachomatis</emph> Infection of the Female Genital Tract
<p><emph>Objective.</emph> The aim of this study was to determine if vaginal application of the immune response modifier imiquimod (Aldara cream, 3M Pharmaceuticals, St Paul, Minn) would alter the course and/or outcome of female genital tract infection with a human isolate of <...
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2006-01-01
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Series: | Infectious Diseases in Obstetrics and Gynecology |
Online Access: | http://www.hindawi.com/GetArticle.aspx?doi=10.1155/IDOG/2006/61265 |
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doaj-90ea8b9d54324d93a0fcef59dede69282020-11-24T23:04:54ZengHindawi LimitedInfectious Diseases in Obstetrics and Gynecology1064-74492006-01-012006Efficacy of an Immune Modulator in Experimental <emph>Chlamydia trachomatis</emph> Infection of the Female Genital Tract<p><emph>Objective.</emph> The aim of this study was to determine if vaginal application of the immune response modifier imiquimod (Aldara cream, 3M Pharmaceuticals, St Paul, Minn) would alter the course and/or outcome of female genital tract infection with a human isolate of <emph>Chlamydia trachomatis</emph> in a murine model. <emph>Methods.</emph> Groups of CF-1 mice were treated with Aldara on three different schedules: (1) ongoing beginning 5 days prior to and continuing through day 5 of infection; (2) a single prophylactic dose 2 hours prior to infection; and (3) therapeutic from day 4 to day 14 of infection. Mice were infected vaginally with a serovar D strain of <emph>C trachomatis</emph>, and monitored by culture to determine the level of shedding and duration of infection. <emph>Results.</emph> We observed a significant reduction in both duration of infection and the level of shedding during the acute phase in mice treated on an ongoing basis commencing 5 days prior to infection. There was no effect with respect to the other regimens. <emph>Conclusion.</emph> These results demonstrate that ongoing Aldara treatment has efficacy and may enhance local innate immunity which reduces the duration of subsequent infection with human isolates of <emph>C trachomatis</emph> in a murine model of female genital tract infection.</p>http://www.hindawi.com/GetArticle.aspx?doi=10.1155/IDOG/2006/61265 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
title |
Efficacy of an Immune Modulator in Experimental <emph>Chlamydia trachomatis</emph> Infection of the Female Genital Tract |
spellingShingle |
Efficacy of an Immune Modulator in Experimental <emph>Chlamydia trachomatis</emph> Infection of the Female Genital Tract Infectious Diseases in Obstetrics and Gynecology |
title_short |
Efficacy of an Immune Modulator in Experimental <emph>Chlamydia trachomatis</emph> Infection of the Female Genital Tract |
title_full |
Efficacy of an Immune Modulator in Experimental <emph>Chlamydia trachomatis</emph> Infection of the Female Genital Tract |
title_fullStr |
Efficacy of an Immune Modulator in Experimental <emph>Chlamydia trachomatis</emph> Infection of the Female Genital Tract |
title_full_unstemmed |
Efficacy of an Immune Modulator in Experimental <emph>Chlamydia trachomatis</emph> Infection of the Female Genital Tract |
title_sort |
efficacy of an immune modulator in experimental <emph>chlamydia trachomatis</emph> infection of the female genital tract |
publisher |
Hindawi Limited |
series |
Infectious Diseases in Obstetrics and Gynecology |
issn |
1064-7449 |
publishDate |
2006-01-01 |
description |
<p><emph>Objective.</emph> The aim of this study was to determine if vaginal application of the immune response modifier imiquimod (Aldara cream, 3M Pharmaceuticals, St Paul, Minn) would alter the course and/or outcome of female genital tract infection with a human isolate of <emph>Chlamydia trachomatis</emph> in a murine model. <emph>Methods.</emph> Groups of CF-1 mice were treated with Aldara on three different schedules: (1) ongoing beginning 5 days prior to and continuing through day 5 of infection; (2) a single prophylactic dose 2 hours prior to infection; and (3) therapeutic from day 4 to day 14 of infection. Mice were infected vaginally with a serovar D strain of <emph>C trachomatis</emph>, and monitored by culture to determine the level of shedding and duration of infection. <emph>Results.</emph> We observed a significant reduction in both duration of infection and the level of shedding during the acute phase in mice treated on an ongoing basis commencing 5 days prior to infection. There was no effect with respect to the other regimens. <emph>Conclusion.</emph> These results demonstrate that ongoing Aldara treatment has efficacy and may enhance local innate immunity which reduces the duration of subsequent infection with human isolates of <emph>C trachomatis</emph> in a murine model of female genital tract infection.</p> |
url |
http://www.hindawi.com/GetArticle.aspx?doi=10.1155/IDOG/2006/61265 |
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1725628662475128832 |