Overview

Systems Biology of Flu Vaccine in Healthy Adults With and Without the Use of Antibiotics

Status:
Completed
Trial end date:
2017-05-26
Target enrollment:
0
Participant gender:
All
Summary
The purpose of the study is to better understand how the use of antibiotics changes micro-organisms in the intestines. The change to micro-organisms in the intestines may change the body's vaccine immune response and alter the effectiveness of the IIV (seasonal flu) vaccine. In particular, the investigators will be looking at certain markers in blood after vaccination with IIV (seasonal flu vaccine) with or without the use of antibiotics before vaccination. There will be two randomized groups. Group A will start taking antibiotic by mouth 3 days prior to vaccination and continue taking antibiotics the day of vaccination and one day after vaccination for a total of 5 days. Group B will only receive the IIV (seasonal flu vaccine) and will not take any antibiotics. The investigators hope to enroll 50 subjects at Emory.
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Emory University
Treatments:
Anti-Bacterial Agents
Antibiotics, Antitubercular
Metronidazole
Neomycin
Vaccines
Vancomycin
Criteria
Inclusion Criteria:

1. Healthy individuals aged 18-40 years.

2. Able to understand and give informed consent.

3. Women of child-bearing potential (not surgically sterile via tubal ligation, bilateral
oophorectomy or hysterectomy or who are not postmenopausal for ≥1 year) must agree to
practice adequate contraception that may include, but is not limited to, abstinence,
monogamous relationship with vasectomized partner, barrier methods such as condoms,
diaphragms, spermicides, intrauterine devices, and licensed hormonal methods for 30
days before and 30 days after TIV vaccination

Exclusion Criteria:

- You received blood product within 3 months of enrolling in the study or a live
attenuated vaccine within 4 weeks or inactivated vaccines within 2 weeks.

- You received the 2014-2015 flu vaccine or had a confirmed case of influenza during
2014-2015.

- You received any antibiotics 6 months prior to enrolling in the study or expect to
take antibiotics one month after vaccination.

- You received probiotics or prebiotics 3 months prior before enrolling in the study or
expect to take one month after vaccination.

- You received proton pump inhibitors, H2 blocker receptors, or antacids 3 months
regularly before enrolling in the study or one month after

- You had an allergic response or sensitivity to past vaccinations.

- You have health conditions that weaken your body's ability to fight infections or you
are taking drugs like steroids that weaken your body's ability to fight
infections.(Some nasal and topical steroids are allowed.).

- You have a chronic medical problem including (but not limited to) insulin dependent
diabetes, severe heart disease including arrhythmias, severe lung disease, auto immune
diseases and or grade 4 uncontrolled hypertension.

- Chronic neurological conditions such as seizure disorder, Parkinson disease,
myasthenia gravis, neuropathy, or histories of encephalopathy, meningitis or
ototoxicity.

- Any history of gastrointestinal disease, kidney or liver diseases.

- Alcohol or drug abuse or psychiatric conditions that in the opinion of the
investigator would compromise your participation in this trial.

- Pregnant or are breast feeding.