In vitro production of lectibody and bispecific antibodies targeting surface glycoproteins of SARS-CoV-2 by the novel off-the-shelf approach
- Funded by Academy of Finland
- Total publications:0 publications
Grant number: unknown
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Key facts
Disease
COVID-19Start & end year
20202022Known Financial Commitments (USD)
$427,522.26Funder
Academy of FinlandPrincipal Investigator
Hideo IwaiResearch Location
FinlandLead Research Institution
University of HelsinkiResearch 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
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
Antibodies play a critical defensive role in virus infections in humans. Vaccine-induced immunity could protect humans from COVID-19 by producing neutralizing antibodies. However, viruses have multiple strategies to evade antiviral immune responses of the host, e.g., by hijacking the host glycosylations systems to coat virus surface with glycans. Whereas neutralizing antibodies bind viral surface proteins, lectins from natural sources are known to have high antiviral activities by binding to the surface glycans on enveloped viruses, including SARS-COV-2. The novel off-the-shelf approach by the protein ligation technology opens a new avenue to produce various lectin-Fc fusion in vitro, termed lectibody. Bispecific lectin-antibodies, which can engage NK cells or T-cells, could inhibit viral infections as well as remove infected cells. The off-the-shelf approach could produce various drug candidates in vitro rapidly and also particularly useful for rapidly emerging infectious diseases.