Safety and efficacy of SARS-CoV-2 antibodies
- Funded by Netherlands Organisation for Health Research and Development (ZonMW)
- Total publications:0 publications
Grant number: 1.01501E+13
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Key facts
Disease
COVID-19Start & end year
20202021Funder
Netherlands Organisation for Health Research and Development (ZonMW)Principal Investigator
Dr BL. HaagmansResearch Location
N/ALead Research Institution
Not availableResearch Priority Alignment
N/A
Research Category
Clinical characterisation and management
Research Subcategory
Supportive care, processes of care and management
Special Interest Tags
N/A
Study Type
Clinical
Clinical Trial Details
Not applicable
Broad Policy Alignment
Pending
Age Group
Unspecified
Vulnerable Population
Other
Occupations of Interest
Unspecified
Abstract
Severely immunocompromised patients, such as organ transplant recipients and patients with hematological malignancies, are at increased risk for severe coronavirus disease 2019 (COVID-19)-related morbidity and mortality. Plasma from COVID-19 infected individuals that contains antibodies that neutralize the virus can be used to treat those patients. However, our results from clinical and animal studies in which plasma was administered showed that the amount of neutralizing antibodies in the donor plasma and the time of administration are critical parameters for treatment effectiveness. In addition, resistance often occurred when monoclonal antibodies were used. Alternatively, we tested plasma obtained from individuals who received multiple COVID-19 vaccinations. Using in vitro assays, we were able to select those individuals with high levels of broadly reactive neutralizing antibodies against different SARSCoV-2 variants for plasma apheresis. These plasma preparations are now being tested in clinical trials to treat hospitalized severely immunocompromised patients. More information about research into corona and COVID-19 at www.zonmw.nl/coronaonderzoek