to leverage mutational antigenic profiling to advance the design of vaccines and therapeutics to SARS-CoV-2, influenza virus and HIV

Grant number: INV-004949

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Key facts

  • Disease

    COVID-19, Unspecified
  • Start & end year

    2020
  • Known Financial Commitments (USD)

    $899,997
  • Funder

    Gates Foundation
  • Research Location

    United States of America
  • Lead Research Institution

    Fred Hutchinson Cancer Center
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics
  • Research Subcategory

    Pathogen genomics, mutations and adaptations
  • Special Interest Tags

    N/A
  • Study Type

    Not applicable
  • Clinical Trial Details

    N/A
  • Broad Policy Alignment

    Pending
  • Age Group

    Not Applicable
  • Vulnerable Population

    Not applicable
  • Occupations of Interest

    Not applicable

Abstract

N/A

11 Publications linked via Europe PMC

Mapping the neutralizing specificity of human anti-HIV serum by deep mutational scanning.

Deep mutational scans for ACE2 binding, RBD expression, and antibody escape in the SARS-CoV-2 Omicron BA.1 and BA.2 receptor-binding domains.

A pseudovirus system enables deep mutational scanning of the full SARS-CoV-2 spike.

Neutralizing monoclonal antibodies elicited by mosaic RBD nanoparticles bind conserved sarbecovirus epitopes.

The SARS-CoV-2 Delta variant induces an antibody response largely focused on class 1 and 2 antibody epitopes.

A SARS-CoV-2 variant elicits an antibody response with a shifted immunodominance hierarchy.

Complete map of SARS-CoV-2 RBD mutations that escape the monoclonal antibody LY-CoV555 and its cocktail with LY-CoV016.

Complete Mapping of Mutations to the SARS-CoV-2 Spike Receptor-Binding Domain that Escape Antibody Recognition.

Comprehensive mapping of mutations in the SARS-CoV-2 receptor-binding domain that affect recognition by polyclonal human plasma antibodies.