Overview
Background
Early evidence in the COVID-19 pandemic suggests that smokers are at a higher risk of having severe effects or dying from the disease. Smoking causes changes in immune cells. Researchers think this may be the reason why smokers are more likely to have severe effects from COVID-19. Researchers want to better understand the interaction between smoking history, the immune system, and COVID-19.
ObjectiveTo better understand how COVID-19 affects smokers and non-smokers immune systems before and after being infected with the virus.
EligibilityHealthy people ages 30-55 who are a smokers or non-smokers who may potentially contract COVID-19
DesignParticipants will be screened over the phone. They will answer questions about their demographics, medical history, medications, and smoking status.
Participants will have up to 6 monthly visits.
At the first visit, participants will have blood tests. Blood will be drawn through a needle in an arm vein. They will provide a saliva sample in a container. Their height and weight will be taken. They will complete questionnaires about their medical history and smoking status.
Participants will then have monthly visits. They will have blood draws to test for COVID-19 antibodies. These visits will occur 4 times or until they have a positive antibody result.
Participants will have a final visit. They will have blood tests.
If at any time participants test positive for a COVID-19, they will be rescheduled 14 days or more after they no longer have symptoms....
Description
Study Description: This study is a prospective, longitudinal, observational, single-center, exploratory study to collect samples and data that will enable explorations of the interaction between smoking, immune system characteristics and Coronavirus Disease 2019 (COVID-19). This study will collect baseline samples and data prior to COVID-19 infection required to explore these interactions prospectively. Early evidence in the COVID-19 pandemic suggests that smokers have higher risk for morbidity and mortality associated with COVID-19 infection. We have identified smoking-associated altered epigenetics, transcription and changes in immune cell profiles. Smoking exposure drives loss of naive CD8+ T cells and increases in senescent CD8+ T cells and these effects are signs of immune system dysfunction. We propose that the immune system senescence associated with prior smoking is a susceptibility factor in COVID-19 morbidity.
ObjectivesPrimary Objective: To prospectively collect biospecimens and data at baseline and longitudinally in an identified fashion from eligible participants and retain for future use to better understand the interaction between smoking history, immune cell profiles and the natural history of COVID-19 morbidity. We hypothesize that senescent CD8 T cells will be higher in smokers who develop COVID-19.
To test this hypothesis, we will establish a bank of cryopreserved peripheral blood mononuclear cells (PBMCs) from before and after COVID-19 exposure from smokers and nonsmokers and use mass cytometry (CyTOF) to analyze detailed immune profiles, test if the frequency of senescent CD8 T cells is higher among smokers who develop COVID-19 (antibody positivity) relative to those who do not develop COVID-19 positivity.
Exploratory Objective: To compare potential immunological biomarkers of susceptibility to viral infection with genetic, epigenetic and other biological characteristics measured in blood before and after recovery from COVID-19 illness and develop assays that indicate immune cell dysfunction and COVID-19 susceptibility.
EndpointsPrimary Endpoint: Levels of senescent CD16+CD8+ T cells before COVID-19 and time to COVID-19 morbidity.
Exploratory Endpoints:
- Smoking exposure biomarkers
- Immune cell profiles identified by CyTOF assays or other single cell assays
- Transcriptional profiles from immune cell subtypes
- DNA methylation profiles of candidate genes in immune cell subtypes
Study Population: Male and female participants aged 30 to 55 years old, generally healthy with a history of smoking (n=60) and nonsmoking (n=30).
Description of Sites/Facilities Enrolling Participants: All visits will be conducted at the NIEHS Clinical Research Unit (CRU) in Durham, North Carolina, USA.
Study Duration: Estimated time from enrollment to completion of data analyses is 24 months.
Participant Duration: Estimated average amount of time for a participant to complete all study visits is 6 months.
Eligibility
- INCLUSION CRITERIA:
In order to be eligible to participate in this study, an individual must meet all of the following criteria:
- Stated willingness to comply with all study procedures and availability for the duration of the study
- Male and females
- Age 30 to 55 years
- Able to travel to study visits at the NIEHS CRU for required study visits
- Body mass index (BMI) range between 18 and 35 at enrollment
- Must self-identify as a current smoker (cigarettes and/or use of an e-cigarette/vaping device), have smoked for 5 years or longer or identify as a non-smoker, having never used of any other forms of tobacco, nicotine, or smoked marijuana and not currently residing with a smoker
EXCLUSION CRITERIA:
An individual who meets any of the following criteria will be excluded from participation in this study:
- History of confirmed COVID-19 infection
- Current diagnosis of cancer or prior history of cancer
- Bleeding disorder or any reason that a blood sample cannot be provided
- Current pregnancy or lactation, by participant verbal confirmation.
- Any condition that, in the investigator's opinion, places the participant at undue risk for complications associated with required study procedures