Official Title
How Immune Responses Shape Virological and Clinical Characteristics of COVID-19: a Prospective Cohort Study
Brief Summary

This single-center prospective observational study will examine immune responses to to SARS-CoV-2 and how they correlate with its virological characteristics and clinical manifestations in infected patients. Household contacts will also be included so that early immune responses and viral kinetics can be captured. Patients and contacts will be followed for 8 and 2 weeks, respectively. The study will include a maximum of 250 participants.

Detailed Description

The primary aim of this single-center prospective observational study is to establish how
immune responses to SARS-CoV-2 or to cross-reactive viruses correlate with the virological
and clinical characteristics of SARS- CoV-2-infected patients and their exposed household
contacts. Through iterative sampling, the viral kinetics of at least 50 infected patients
will be evaluated in relation to symptom severity and innate and adaptive immune responses,
while their household contacts will be observed for viral detection and immune responses.
Patients and contacts will be followed for 8 and 2 weeks, respectively. The study will
include a maximum of 250 participants.

Completed
SARS-CoV-2 Viral Kinetics and Host Immune Responses

Other: NA (no intervention)

NA (no intervention)

Eligibility Criteria

Inclusion Criteria:

The following persons may be included:

- A patient of any age meeting the European Centre for Disease Control and Prevention's
confirmed case definition: "A person with laboratory confirmation of virus causing
COVID-19, irrespective of clinical signs and symptoms" (and/or high suspicion/actively
being treated as CoVID+ cases pending test confirmation)

- Household contacts (defined as those sleeping in the same apartment/house as an
infected patient) of a patient with laboratory-confirmed COVID-19 (and/or high
suspicion/actively being treated as CoVID+ cases pending test confirmation), whether
symptomatic or not, and whether testing positive or not during a period of 14 days

Exclusion Criterion:

- Long-term incapacity leading to the inability to provide informed consent while not
having a patient representative with the ability to provide informed consent

Eligibility Gender
All
Eligibility Age
Minimum: N/A ~ Maximum: N/A
Countries
Switzerland
Locations

University Hospitals of Geneva
Geneva, Switzerland

Claire-Anne Siegrist, MD, Principal Investigator
Professor of vaccinology

University of Geneva, Switzerland
NCT Number