Microbiome Clinical Trial
Official title:
Microbiomic and Immunologic Profiling of Women With Antibiotic Induced Vaginal Candidiasis
Background:
- Vaginal yeast infections are caused by a fungus called Candida. Candida can live harmlessly
in the vagina, but most women will have symptoms from a vaginal yeast infection at some point
during their life. Antibiotics increase the risk for yeast infections, but it is unclear why.
They may disrupt the balance of healthy bacteria in the vagina. This could make it harder for
the body to fight off yeast infections. Researchers will give healthy women a common
antibiotic or a placebo. They will study how the antibiotic affects bacteria and yeast in the
vagina and other parts of the body. This will let researchers study the normal changes of
healthy bacteria and yeast over time.
Objectives:
- To see how the study drug changes healthy bacteria in the vagina, and how these changes may
increase the risk for yeast infections.
Eligibility:
- Healthy women ages 18 to 40 who are not allergic to penicillin.
Design:
- Participants will be screened with medical history, physical exam (including vaginal
exam), blood tests and tests for sexually transmitted diseases.
- Participants must take birth control pills for at least 3 months before, and during the
study.
- Participants will take the study antibiotic or placebo for 10 days.
- Participants will have 7 study visits over 3 months. Visits will be timed around
participants menstrual cycles.
- At the visits, participants will answer questions about their health and undergo tests.
These may include swabs of the vagina, mouth and skin as well as blood tests. Vaginal
fluid, saliva and urine will also be collected.
- Between visits, participants will collect stool and vaginal samples at home and bring
them to the next clinic visit.
This protocol is a prospective, interventional, randomized, double-blind, placebo controlled
longitudinal study designed to investigate the microbiomic and immunologic perturbations that
lead to vulvovaginal candidiasis (VVC) in women who receive antibiotics. VVC is the most
common fungal infection affecting women. Although asymptomatic vaginal Candida colonization
occurs in ~10-20% of healthy women, ~75% of women will experience at least one episode of
symptomatic VVC during their lifetime. Nonetheless, the local mucosal factors that allow
Candida to convert from a commensal organism to an opportunistic pathogen are not well
defined. Antibiotic use (particularly beta-lactams) is a well-recognized risk factor for the
development of VVC in healthy women, suggesting that alterations in the endogenous vaginal
microbial flora results in deregulation of local mucosal anti-Candida immune responses.
However, which commensal vaginal microbiota are important for protection against Candida
infection, and the mechanism(s) whereby vaginal microbiota influence the local mucosal immune
response against Candida, remain unknown.
To address these questions, healthy women of reproductive age will receive a 10-day course of
amoxicillin (a broad-spectrum, beta-lactam antibiotic) or a placeboand will undergo vaginal
sampling for microbiomic and immunologic analyses before, during and after antibiotic
administration over a 90-day period. The hypothesis of this study is that women who develop
amoxicillin-associated VVC will have a characteristic microbiomic profile (as compared to
women with absent or asymptomatic Candida colonization) with associated impairment in local
mucosal anti-Candida immune responses. The aim of this study is to elucidate the vaginal
microbiomic and immunologic perturbations that allow Candida to transition from commensal to
pathogen in the context of antibiotic administration. A better understanding of the role of
specific microbiota and mucosal immune factors in averting Candida infection may lead to the
design of targeted preventive and/or therapeutic interventions against VVC.
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