Mary Ellen Jones
Chapel Hill, North Carolina, 27599, United States
Location status: Recruiting
NCT Number: NCT06841913
This study will investigate the effects of woodsmoke (WS) exposure on human nasal mucosal immune responses to viral infection. The study tests the hypotheses that WS exposure modifies biomarkers of nasal mucosal immune function, increases in Live Attenuated Influenza Virus (LAIV) -induced nasal symptoms, and reduces mucosal antibody production.
Interested in participating?
Request Info18 year–49 year
All sexes
Interventional
Phase 4
Chapel Hill, North Carolina, 27599, United States
Location status: Recruiting
This study will investigate the effects of woodsmoke (WS) exposure on human nasal mucosal immune responses to viral infection. The study tests the hypotheses that WS exposure modifies biomarkers of nasal mucosal immune function, increases LAIV-induced nasal symptoms, and reduces mucosal antibody production. Healthy volunteers will be randomized for a 2-hr exposure to WS or placebo (filtered air) and then inoculated with either live attenuated influenza virus (LAIV) or placebo. Nasal mucosal samples, symptoms, and peripheral blood will be collected on days 1,2,3,7, and 21 post-exposure/LAIV and assessed for a) mucosal antiviral responses using targeted and non-targeted analysis of the secretome and tissue-level gene expression; b) symptoms, virus quantity, differential cell count, and virus-specific antibody levels; and c) biomarker signatures associated with infection outcomes using computational modeling tools.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Inoculation with LAIV
Other names: Live Attenuated Influenza Vaccine, Flumist
Wood smoke exposure concentrations at 500 ug/m3 for two hours.
Placebo for LAIV inoculation. Nasal administration of normal saline.
Clean Air Exposure for 2 hours
Time frame: Day 0 to Day 7
Analysis of the nasal mucosal secretome (secreted factors identified as responsive to WS and/or LAIV). Area under the curve (AUC) will be calculated for each proteomic profile. Descriptive statistics (means and standard deviations) will be computed for outcomes of interest (AUCs), assuming normal distribution as in previous studies.
Time frame: Day 0 to Day 7
Tissue-level gene expression (genes identified as responsive to WS and/or LAIV) and assessed for: tissue-level gene expression and untargeted metabolomic and proteomic profiles. Area under the curve (AUC) will be calculated for each gene profile. Descriptive statistics (means and standard deviations) will be computed for outcomes of interest (AUCs), assuming normal distribution as in previous studies.
Time frame: Day 0 to Day 7
Virus quantity in nasal secretions
Time frame: Day 0 to Day 7
nasal secretion
Time frame: Day 0 to Day 7
virus-specific antibody levels in nasal secretions
Time frame: Day 0 to Day 7
virus-specific antibody levels in blood
Time frame: Day 0 to Day 21
Peak value of Tissue-level gene expression (genes identified as responsive to WS and/or LAIV)
Time frame: Day 0 to Day 21
Peak Analysis value of the nasal mucosal secretome (secreted factors identified as responsive to WS and/or LAIV)
Time frame: Day 0 to day 21
Peak value of Virus quantity in nasal secretions
Time frame: Day 0 to Day 21
Peak value of nasal neutrophils
Time frame: Day 0 to Day 21
Peak value of virus-specific antibody levels in nasal secretions
Time frame: Day 0 to Day 21
Peak value of virus-specific antibody levels in blood
Time frame: Day 0 to Day 21
Peak Day of Tissue-level gene expression (genes identified as responsive to WS and/or LAIV)
Time frame: Day 0 to Day 21
Peak Analysis Day of the nasal mucosal secretome (secreted factors identified as responsive to WS and/or LAIV)
Time frame: Day 0 to day 21
Peak Day of Virus quantity in nasal secretions
Time frame: Day 0 to Day 21
Peak Day of nasal secretion
Time frame: Day 0 to Day 21
Peak day of virus-specific antibody levels in nasal secretions
Time frame: Day 0 to Day 21
Peak Day of virus-specific antibody levels in blood
Time frame: Day 0-21
Flu symptom questionnaire. A score from 0-18 will be recorded. Zero being symptom free and 18 the most symptomatic.
Time frame: Day 0-21
Flu symptom questionnaire. A score from 0-18 will be recorded. Zero being symptom free and 18 the most symptomatic. The day in which there is the highest score will be recorded.
Contact information is provided by the study sponsor or research team.
University of North Carolina, Chapel Hill
Other
The Effects of Woodsmoke Exposure on Nasal Immune Responses to Influenza Infection in Normal Human Volunteers
Acronym: SmokeyFlu
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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