Safety and efficacy of SARS-CoV-2 antibodies

  • Funded by Netherlands Organisation for Health Research and Development (ZonMW)
  • Total publications:22 publications

Grant number: 10150062010008

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2021
  • Funder

    Netherlands Organisation for Health Research and Development (ZonMW)
  • Principal Investigator

    Dr BL. Haagmans
  • Research Location

    N/A
  • Lead Research Institution

    Not available
  • Research 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

22 Publications linked via Europe PMC

Revealing the significance of IL-2 and IL-5 in SARS-CoV-2-specific T-cell responses in kidney transplant recipients.

SARS-CoV-2 Omicron entry is type II transmembrane serine protease-mediated in human airway and intestinal organoid models.

Divergent SARS-CoV-2 Omicron-reactive T and B cell responses in COVID-19 vaccine recipients.

Antigenic cartography of SARS-CoV-2 reveals that Omicron BA.1 and BA.2 are antigenically distinct.

Omicron BA.1 and BA.2 are antigenically distinct SARS-CoV-2 variants

Seasonal coronavirus-specific B cells with limited SARS-CoV-2 cross-reactivity dominate the IgG response in severe COVID-19.

SARS-CoV-2 Omicron efficiently infects human airway, but not alveolar epithelium

Divergent SARS CoV-2 Omicron-specific T- and B-cell responses in COVID-19 vaccine recipients

A CRISPR/Cas9 genetically engineered organoid biobank reveals essential host factors for coronaviruses.