Macrophage Regulation of Ozone-Induced Lung Inflammation

Description

The purpose of this research study to understand how prior respiratory infections affect the susceptibility to lung inflammation following environmental exposures.

Conditions

SARS-CoV-2 Pneumonia

Study Overview

Study Details

Study overview

The purpose of this research study to understand how prior respiratory infections affect the susceptibility to lung inflammation following environmental exposures.

Macrophage Regulation of Ozone-Induced Lung Inflammation

Macrophage Regulation of Ozone-Induced Lung Inflammation

Condition
SARS-CoV-2 Pneumonia
Intervention / Treatment

-

Contacts and Locations

Durham

Duke University Medical Center, Durham, North Carolina, United States, 27710

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Individuals between 18-55 yrs. of age (No subject will be excluded from the study on the basis of gender or ethnicity)
  • * Individuals with knowledge of prior SARS-CoV-2 infection history allowing them to be segregated into one of three cohorts
  • * Cohort 1 - No history of SARS-CoV-2 infection (defined as no symptoms consisted with SARS-CoV-2 nor history of a positive SARS-CoV-2 test)
  • * Cohort 2 - Documented mild SARS-CoV-2 infection (a positive test, either PCR- or antigen-based) but with mild to no symptoms and no evidence of a lower respiratory tract infection (including no hospitalization, and no oxygen use)
  • * Cohort 3 - History of SARS-CoV-2 infection and symptoms/imaging consistent with a lower respiratory tract infection who have recovered, are \>6 months out from their infection, and have normal lung function (spirometry with FVC, FEV1 and FEV1/FVC)
  • * There will be no maximal period from SARS-CoV-2 infection for inclusion in the study, the minimal period will be \>6 months out from infection
  • * Individuals with prior SARS-CoV-2 pneumonia who have ongoing respiratory symptoms, are still using supplemental oxygen, or have abnormal lung function
  • * Individuals with prior SARS-CoV-2 infection that cannot provide documentation of a positive test
  • * Current smokers of tobacco products including e-cigarettes or those with previous smoking history within the prior 5 years
  • * Pregnant women and women who are presently lactating.
  • * Subjects that have received antibiotic administration or an upper respiratory infection within the previous 4 weeks
  • * College and graduate students or employees who are under direct supervision by any of the investigators in this protocol
  • * Alcohol or illicit substance abuse
  • * Chronic cardio/pulmonary respiratory disorders or other medical conditions as determined by the investigator
  • * Increased airway hyperresponsiveness at baseline as measured by a positive methacholine challenge response (methacholine PC20 FEV1 \< 4 mg/ml)
  • * Subjects will be requested to refrain from antihistamines, nonsteroidal anti-inflammatory agents, antioxidants (e.g. beta-carotene, selenium, and lutein) and supplemental vitamins (e.g. C and E), for 1 week prior to, and during testing.

Ages Eligible for Study

18 Years to 55 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Robert Tighe, MD,

Robert Tighe, MD, PRINCIPAL_INVESTIGATOR, Duke University

Study Record Dates

2028-05