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COVID-19 Vaccine Induced Immunity

U

University of Manitoba

Status

Unknown

Conditions

Covid19

Treatments

Drug: covid19 vaccine

Study type

Observational

Funder types

Other

Identifiers

NCT04713163
B2021:008

Details and patient eligibility

About

This study aims to address the following three objectives:

  1. Longitudinal evaluation of the development of CMI responses in response to SARS-CoV-2 Vaccine: T cells isolated from the blood of COVID-19 vaccine recipients will be evaluated for their functionality in response to vaccine antigens. The temporal and functional properties of CMI responses will be correlated with the humoral or antibody responsiveness. CMI responses will be measured in vaccine recipients prior to vaccination to determine whether the presence or functionality of pre-existing responses to common cold coronaviruses (CCCs) or previous SARS-CoV-2 infections affect the development of CMI responses to the COVID-19 vaccine.

  2. Identification of cellular and soluble factors that influence vaccine responsiveness:

    While it is known that poor clinical outcomes in COVID-19 patients are strongly associated with markers of systemic inflammation, the influence these systemic markers will have on COVID-19 vaccine responsiveness is not clear. Using systems biology approaches, the investigators will perform comprehensive profiling of cellular immune subsets, inflammatory signatures to identify determinants influencing the development of CMI responses to vaccine.

  3. Examine variability of immune and viral genes and their relationship to vaccine induced immune responses: Human leukocyte antigen (HLA), T cell receptor (TCR) and B cell receptor (BCR) proteins are highly genetically diverse and critical to development of protective immunity. The investigators will perform HLA sequencing on whole blood-derived DNA samples and TCR and BCR sequencing on sorted, SARS-CoV2 vaccine antigen-specific T cells and B cells, respectively, to assess how different sequence combinations impact the CMI responses to vaccine.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • all individuals eligible to receive one of the approved SARS-CoV-2/COVID-19 vaccines.

Exclusion criteria

  • individuals under 18 years of age

Trial design

200 participants in 2 patient groups

Health care or laboratory-based workers
Description:
Healthy individuals about to receive any approved COVID-19 vaccine
Treatment:
Drug: covid19 vaccine
Outpatients
Description:
Outpatients about to receive any approved COVID-19 vaccine
Treatment:
Drug: covid19 vaccine

Trial documents
1

Trial contacts and locations

0

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Central trial contact

Lyle R Mckinnon, PhD; Blake Ball, PhD

Data sourced from clinicaltrials.gov

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