Influenza
Conditions
Keywords
immunology, Microbiota
Brief summary
This study will serve to determine how influenza infection alters the bacterial colonization patterns in the nasal and oropharyngeal compartments, and whether the immune response correlate with these alterations. The investigators will be determining bacterial composition and immune responses in the nose and oropharynx during influenza infection. Specific Aims Therefore, the overall aims of this study are as follows: 1. To identify baseline composition and kinetic changes in the nasal and oropharyngeal microflora and immune responses after administering intranasal live attenuated influenza virus (i.e., FluMist® vaccine) or saline mist to healthy subjects; 2. To identify nasal and oropharyngeal microbial composition and local immune responses during influenza infections and after resolution of infection, and correlate these changes with clinical outcomes.
Detailed description
Randomization and Post-Randomization Visits After undergoing the nasal swabs and nasopharyngeal washes, and nasal epithelial brushing, healthy volunteers will be randomly assigned to receive either saline nasal spray (placebo) or FluMist® nasal influenza vaccine (live attenuated influenza vaccine, or LAIV). They will return 1-2 weeks and 4-6 weeks later to repeat the nasal swabs and nasopharyngeal washes, and nasal epithelial brushings done at the Enrollment Visit. Samples will be processed to isolate 16s bacterial RNA and host RNA. 16s rRNA will be analyzed by 16S sequencing for to determine the composition of the bacterial microbiome pre and post LAIV or saline (placebo) administration. Host immune responses will be assessed based upon microarray analysis of host RNA pre and post LAIV or saline administration.
Interventions
BIOLOGICALLAIV
Subjects underwent nasal swabs, nasopharyngeal saline wash, and nasal brushings pre, and 1-2 weeks and 4-6 weeks following intranasal administration of LAIV.
OTHERSaline
Subjects underwent nasal swabs, nasopharyngeal saline wash, and nasal brushings pre, and 1-2 weeks and 4-6 weeks following intranasal administration of saline nasal spray.
Sponsors
University of California, Los Angeles
J. Craig Venter Institute
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
Yes
Inclusion criteria
* Healthy volunteers: * Healthy subjects between the ages of 18 and 65. Approximately half of the subjects will be female and approximately half will be male. * Must be eligible to receive live-attenuated nasal version of the influenza vaccine. * Must be able to provide signed and dated informed consent. * Healthy subjects willing and able to provide oropharyngeal and nasal cavity specimens
Exclusion criteria
* Immunosuppressive conditions or medications * chronic systemic medical illness * infections or antibiotic use within the past 60 days
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in the bacterial composition (Bacterial "microbiome") over time | Changes from baseline at 1-2 weeks and 4-6 weeks after LAIV or saline spray | isolation of 16S RNA from nasal swabs and nasopharyngeal washes for 16S sequencing for bacterial microbiome |
| Changes in gene expression in the nasal lining of study participants | Changes from baseline at 1-2 weeks after LAIV or saline spray | RNA isolation from nasal brushes which will undergo microarray analysis to measure changes in immune gene expression |
Countries
United States
Outcome results
None listed