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Allergic RhinitisFLAIRNCT00617110

Effects of Diesel Exhaust Followed by Administration of Nasal Spray Flu Vaccine on Individuals With & Without Allergies

A study testing live attenuated influenza virus (LAIV) with clean air and LAIV and diesel exhaust particles in people with Allergic Rhinitis, run by University of North Carolina, Chapel Hill at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Allergic rhinitis (AR) is a condition that exists when an individual with a specific allergy reacts to that allergen resulting in a runny and/or stuffy nose, postnasal drip, and possible symptoms of sneezing, scratchy throat, itchy nose, ears or throat. Read more about this study

Who is it for?
Ages 18 to 35 yearsHealthy volunteers can take part
Conditions the study is for
Allergic Rhinitis
What is being tested?
live attenuated influenza virus (LAIV) with clean air and LAIV and diesel exhaust particles
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
54 participants
Where
1 siteUnited States
Study dates
Jan 2008to Apr 2014
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Normal lung function, defined as (Knudsen 1976/1984 predicted set):
  • FVC of > 75 % of that predicted for gender, ethnicity, age and height
  • FEV1 of > 75 % of that predicted for gender, ethnicity, age and height
  • FEV1/FVC ratio of .70
  • Oxygen saturation of > 94 %
  • Normal blood pressure (Systolic between 140 - 90, Diastolic between 90-60 mm Hg)
  • Symptom Score no greater than 6 (out of a possible 39) for total symptom score
  • On the day of a challenge, body temperature must be no greater than 37.8 degrees, measured orally

Who cannot join

  • A history of significant chronic illnesses (to include diabetes, autoimmune diseases, immunodeficiency state, known ischemic heart disease, chronic respiratory diseases such as chronic obstructive pulmonary disease or asthma, hypertension)
  • Allergy to any medications which may be used in the course of this study (albuterol, acetaminophen, aspirin or non-steroidal anti-inflammatory agents, corticosteroids)
  • Positive pregnancy test within 48 hours of the time of challenge
  • Medications which may impact the results of the experimental viral infection, interfere with any other medications potentially used in the study (to include nasal or oral corticosteroids, beta adrenergic antagonists, non-steroidal anti-inflammatory agents) or suggest an ongoing illness (such as antibiotics)
  • Acute, non-chronic, medical conditions, including (but not limited to) pneumonia or bronchitis requiring antibiotics, febrile illnesses, flu-like symptoms must be totally resolved symptomatically for 3 weeks
  • Unspecified illnesses, which in the judgment of the investigator increase the risk associated with the experimental LAIV infection, will be a basis for exclusion
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  • Use of any inhaled substance (for medical or recreational purposes)
  • Receipt of flu vaccine of any type (injection or nasal spray) during the prior season (2006/2007)
  • Current use of allergy immunotherapy ("allergy shots")

Trial locations and contacts

1 site in 1 country.

United States1 site
  • US EPA Human Studies Facility

    Chapel Hill, North Carolina, 27514

Other trials in United States

About this study

Official title: Effects of Diesel Exhaust Particles on Influenza-induced Nasal Inflammation in Allergic Rhinitics and Non-allergic Individuals

Allergic rhinitis (AR) is a condition that exists when an individual with a specific allergy reacts to that allergen resulting in a runny and/or stuffy nose, postnasal drip, and possible symptoms of sneezing, scratchy throat, itchy nose, ears or throat. When the allergic person is exposed to such an allergen, the body reacts with overproduction of certain chemicals which cause inflammation and subsequent symptoms of AR. These responses are related to the body's hyperreactive response to exposure to an otherwise harmless substance such as dust, ragweed, pollen, cat dander etc.

There are data to suggest that air pollution resulting from diesel exhaust can increase the body's response to airway inflammation caused by virus.

The purpose of this research study is to determine if individuals with AR have increased inflammatory responses to flu virus following exposure to diesel exhaust (DE) vs exposure to clean air compared to how individuals who do not have allergies respond to the same exposure conditions. The hypothesis for this study is that diesel exhaust exacerbates LAIV-induced allergic nasal inflammation, using controlled exposures in AR volunteers compared to non-allergic individuals

Read the detailed description

Screening day: This visit will occur approximately 2-4 weeks before your exposure day. You will come to the research facility where you will discuss this consent form with the study coordinator and complete the signature areas. Your vital signs (pulse, temperature, BP, oxygenation saturation) will be measured and the following evaluations will be performed:

  • For females of child bearing potential, a urine pregnancy test
  • Review your medical history and any recent health changes
  • Completion of a questionnaire regarding your allergy symptoms
  • Collection of spirometric (pulmonary function testing) data will be performed. You must demonstrate normal pulmonary function in order to continue in the study. You will be asked to inhale as deeply as possible, then exhale as rapidly and completely as possible into a mouthpiece which is connected to a computer which measures various lung volumes and which will tell us if your lung function is normal.
  • Blood draw from a hand or arm vein to test for HIV and recent influenza exposure, as well as serum markers, T cell stimulation and WBC characterization. The volume of blood will be up to 50 cc (approximately 3 tablespoons).
  • A buccal swab will be performed for genotyping which entails rubbing a toothbrush on the inside of your cheeks to loosen the cells followed by repeating the rubbing in the same place with a soft swab (similar to a Q tip® with a longer stick).
  • Physical examination by a study physician
  • Allergy skin test if this has not been performed during the previous 2 years
  • Collection of nasal lavage fluid which will involve spraying some salt water into your nose repeatedly and then blowing your nose into a cup
  • Nasal biopsy during which the researcher gently scrapes the inside lining of your nose with a plastic stick

Day 0 (Monday): You will be asked to eat a light breakfast and arrive at the EPA in early to mid morning. You will need to wear comfortable clothes and shoes, and bring a lunch.

  • Collection of vital sign measurements and update in medical condition as well as medications taken since the previous visit
  • Urine pregnancy test, if applicable
  • A telemetry monitor will be placed so that your heart rhythm can be monitored during your chamber exposure. This will include having monitor wires attached to your chest and shoulders with an adhesive pad. The other end of the wires is connected to a box that can be tied to your waste and which will transmit your heart rhythm to a screen so we can observe it
  • Spirometry measurements: This test measures the volume of air that can be exhaled and the rate of airflow during exhalation after a maximal inhalation. You will inhale as deeply as possible, then exhale as rapidly and completely as possible into the spirometer. Measurements obtained from each maneuver include the forced vital capacity (FVC), the forced expiratory volume in the first second (FEV1), the maximal mid-expiratory flow rate (FEF 25-75%) and the peak flow (PF). The largest FVC and FEV1, from at least 3 acceptable trials, are selected for analysis; the flow rates are selected from the trial with the largest sum of FVC.
  • Nasal lavage
  • You will have a 2 hour exposure to either diesel particles or air. The type of exposure you will receive will be randomized, meaning that you will be assigned to the air or diesel exposure group by chance, like flipping a coin. The exposure will be double blind which means that neither you nor the study investigators and staff will know whether you are being exposed to diesel exhaust or air except in the event of any emergency when this information could be revealed. If you are randomized to receive a diesel exposure, the diesel will be generated from an engine mounted on a vehicle located outside of the EPA Human studies Facility (HSF). The diesel exhaust (DE) is then introduced into the exposure chamber after dilution with clean filtered and humidified air by approximately 1/30th to give a chamber concentration of approximately 100 μg/m3. The amount of DE used for exposure in this study would be equivalent to concentrations encountered at busy intersections in large urban areas. DE concentrations proposed are below occupational levels for some truck drivers (generally about 100-300 µg/m3) and 1-2 mg/m3 for some mines. Some areas of heavily trafficked streets in Los Angeles and New York City have had DE levels > 20 µg/m3, and nearby residents could have exposure to these concentrations over several hours. If you are randomized to clean air, you will receive Chapel Hill air which has been filtered to remove ambient air pollutants
  • After your exposure you will have additional spirometry testing and return to the medical station where you will be monitored for 3 hours. You will also have time to eat your lunch which we are requesting that you bring with you from home
  • Both before and after your exposure, the level of carbon monoxide in your blood will be tested
  • Three hours after your exposure is complete, the FluMist® vaccine will be administered by spraying the vaccine once into each nostril. Shortly after that you will be discharged home

Days 1-3 (Tuesday-Thursday). Each day, the following will be obtained:

  • Vital signs and update any changes in medical condition
  • Nasal lavage

Day 4 (Friday):

  • Vital signs and medical update
  • Nasal lavage
  • Nasal biopsy
  • Blood draw - serum markers, WBC characterization. The volume of blood will be up to 50cc (approximately 3 tablespoons)

Day 9 +/- 1 day (one visit sometime between the Tuesday through Thursday after the week you have received the FluMist®):

  • Vital signs and health update
  • Nasal lavage

Day 21 +/-7 days after the FluMist dose

  • Vital signs and health update
  • Urine pregnancy test, if applicable
  • Blood draw to check your post -vaccine anti-influenza titer, as well as serum markers, T cell stimulation and WBC characterization. The volume of blood will be up to 50 cc (approximately 3 tablespoons)
Being tested
live attenuated influenza virus (LAIV) with clean air, LAIV and diesel exhaust particles
Keywords
diesel exhaust particles, live attenuated influenza virus vaccine, flu vaccine
Medical subject headings
Rhinitis, Allergic, Influenza, Human

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • live attenuated influenza virus (LAIV) with clean airOther

    Also called FluMist

    Allergic subjects will be exposed to air followed by administration of live attenuated influenza virus

  • LAIV and diesel exhaust particlesOther

    Also called FLuMist

    subjects with allergic rhinitis will be exposed to diesel exhaust particles followed by LAIV

Study groups in NCT00617110
Study groupRoleWhat they receive
allergic clean airSham comparatorsubjects with allergic rhinitis will be exposed to clean air followed by LAIV
Receives: Other: live attenuated influenza virus (LAIV) with clean air
Allergic dieselActive comparatorsubjects with allergic rhinitis will be exposed to diesel exhaust particles followed by LAIV
Receives: Other: LAIV and diesel exhaust particles
control clean airSham comparatorHealthy control subjects will be exposed to clean air followed by LAIV
Receives: Other: live attenuated influenza virus (LAIV) with clean air
Control dieselSham comparatorHealthy control will be exposed to diesel followed by LAIV
Receives: Other: LAIV and diesel exhaust particles

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in IL-13 and ECP in nasal lavage fluids (NLF) compared to pre-virus baseline

    Measured: 1-21 days post challenge

Secondary outcomes (7)
  1. Duration/quantity of virus shedding

    Measured: 0-21 days post challenge

  2. Change in inflammatory cells in NLF at specific time points compared to baseline

    Measured: 0-21 days post challenge

  3. Change in inflammatory cytokines/chemokines and other mediators (PGE2, tryptase, MPO, adenosine) in NLF at specific time points compared to baseline

    Measured: 0-21 days post challenge

  4. Post LAIV change in overall "oxidative stress" in nasal epithelial cells

    Measured: 0-21 days post challenge

  5. Post LAIV change in epithelial gene expression profiles for innate immune and oxidant/antioxidant network arrays in nasal epithelial biopsies

    Measured: 0-21 days post challenge

  6. Change in levels and activities of circulating white blood cells, including eosinophils, basophils, monocytes, and lymphocytes

    Measured: 0-21 days post challenge

  7. Outcomes for GSTM1 null vs. sufficient genotype individuals

    Measured: 0-21 days post challenge

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Feb 2008 (estimated)
  2. Study startJan 2008
  3. Primary completionMar 2014
  4. Study completionApr 2014

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
54 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00617110
Sponsor's protocol ID
07-1064
Other IDs
2R01ES013611
Acronym
FLAIR
Status last verified
Jun 2015
First submitted
5 Feb 2008
Last updated
3 Jun 2015
Results posted
No
Data monitoring committee
No

Publications

  • Pawlak EA, Noah TL, Zhou H, Chehrazi C, Robinette C, Diaz-Sanchez D, Muller L, Jaspers I. Diesel exposure suppresses natural killer cell function and resolution of eosinophil inflammation: a randomized controlled trial of exposure in allergic rhinitics. Part Fibre Toxicol. 2016 May 6;13(1):24. doi: 10.1186/s12989-016-0135-7.

    PubMed 27154411
  • Noah TL, Zhou H, Zhang H, Horvath K, Robinette C, Kesic M, Meyer M, Diaz-Sanchez D, Jaspers I. Diesel exhaust exposure and nasal response to attenuated influenza in normal and allergic volunteers. Am J Respir Crit Care Med. 2012 Jan 15;185(2):179-85. doi: 10.1164/rccm.201103-0465OC. Epub 2011 Oct 27.

    PubMed 22071326

Questions about this trial

What is this clinical trial studying?

A study testing live attenuated influenza virus (LAIV) with clean air and LAIV and diesel exhaust particles in people with Allergic Rhinitis, run by University of North Carolina, Chapel Hill at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Jun 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in IL-13 and ECP in nasal lavage fluids (NLF) compared to pre-virus baseline (time frame: 1-21 days post challenge). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00617110, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Jun 2015.

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