A Novel High Throughput Assay To Measure Plasma Neutralizing Activity Against Sars-cov-2 (NEUTRACOV)
- Funded by Luxembourg National Research Fund
- Total publications:0 publications
Grant number: unknown
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Key facts
Disease
COVID-19Known Financial Commitments (USD)
$54,000Funder
Luxembourg National Research FundPrincipal Investigator
Danielle Perez BercoffResearch Location
LuxembourgLead Research Institution
Luxembourg Institute of Health (LIH)Research Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Diagnostics
Special Interest Tags
N/A
Study Type
Non-Clinical
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Not Applicable
Vulnerable Population
Not applicable
Occupations of Interest
Not applicable
Abstract
There is currently is no vaccine and no specific antiviral agent against coronaviruses. Existing antiviral drugs against other viruses are being repurposed to treat COVID-19 patients as best we can. In many countries including Luxembourg, hospitals might face a shortage in medication on top of hospital saturation and economic lockdown. Therefore alternative treatment options are urgently needed and many efforts are being deployed to develop a vaccine against SARS-CoV-2, the new Coronavirus causing COVID-19. Nevertheless, little is known on immunity against SARS-CoV-2 and on the efficacy and persistance of the antibody response. Passive immunization of patients with severe or critical COVID-19 using the plasma from recovered patients (plasmapheresis) is one approach considered to test COVID-19 patients. It has been used in the past to treat other lethal viral infections such as SARS, Flu, Ebola. Clinical protocols of plasmapheresis to treat COVID-19 are being launched in the US, in France and at Centre Hospitalier de Luxembourg (CHL). This project aims to develop a high througput assay to measure the neutralizing activity of plasma and antibodies against SARS-CoV-2. It will be used in the short term to assist CHL by identifying plasma from recovered COVID-19 patients with high neutralizing activity for plasmapheresis. It will also be used to identify which antibodies have neutralizing activity, thereby providing a rationale to predict patient outcome. On the mid-long term, it will be used to follow the effectiveness, duration and waning of neutralizing antibodies in patients recovered from COVID-19 and in vaccinated individuals when a vaccine becomes available. Additionnally, it can be used to screan for entry inhibitors, such as Hydrodychlorquine, Lopinavir/ritonavir or novel compounds. It will thus be a useful tool for projects in the COVID-19 Task Force.