Seasonal Coronaviruses: Receptor Binding, Immune Evasion and Cross-species Transmission
- Funded by Canadian Institutes of Health Research (CIHR)
- Total publications:0 publications
Grant number: 504819
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Key facts
Disease
Otherstart year
2024Known Financial Commitments (USD)
$74,271.6Funder
Canadian Institutes of Health Research (CIHR)Principal Investigator
Rini James MResearch Location
CanadaLead Research Institution
University of TorontoResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Pathogen morphology, shedding & natural history
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
Four seasonal coronaviruses are responsible for 15-30% of the human common cold. As with all coronaviruses, the S-proteins of the seasonal coronaviruses are responsible for entry into the cells of the respiratory tract. To mediate this process, the S-proteins must first bind to molecules on the surface of these cells known as "receptors". Among the seasonal coronaviruses, different host proteins and carbohydrates serve as receptors. At the same time, the human immune system produces "neutralizing antibodies" that bind to the S-protein to block its ability to bind its receptors. In this way, antibodies protect us from viral infection and disease. Vast animal coronavirus reservoirs exist in bats, rodents and other animals and the emergence of new viral threats is deemed to be high. The goal of this work is to study the varied ways that the seasonal coronaviruses have evolved to infect humans and evade the immune system. The knowledge gained will serve in the development of therapeutics and vaccines should new coronaviruses cross species barriers to infect humans.