Coronaviral infection COVID-19
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: -written informed consent to participate in the study and store samples -age between 18 and 75 years - PCR confirmed SARS-CoV-2 infection - able to visit the Amsterdam UMC, location AMC 3-8 weeks after onset of COVID-19 symptoms. In the absence of symptoms, patients will visit the Amsterdam UMC, location AMC 3-8 weeks after PCR confirmation. A home visit by the study team is a possibility when the patient is unable to travel to the Amsterdam UMC.
Exclusion criteria
Exclusion criteria: -mental disorder that in the view of the investigator would interfere with adherence to the treatment or the study procedures, or the decision to participate in the study. -use of immunosuppressive medication (equivalent of > 7.5mg prednisolone / day). Note: Patients with only a short course of immunosuppressive medication can still participate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| For objective 1, the main endpoints are the percentage COVID-19 spike protein positive memory B cells and the neutralization potency of monoclonal antibodies derived from COVID-19 spike protein positive memory B cells. For objective 2 the main endpoint are the percentage Coronavirus (CoV) cross-reactive memory B cells and the neutralization potency and breadth of monoclonal antibodies derived from CoV cross-reactive memory B cells. | — |
Countries
Netherlands