Detection and sequencing of SARS-CoV-2 derived HLA-I bound antigenic peptides in the blood of COVID-19 patients: mapping the CD8 T cell response.
- Funded by UK Research and Innovation (UKRI)
- Total publications:1 publications
Grant number: MR/V035851/1
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Key facts
Disease
COVID-19Start & end year
20202022Known Financial Commitments (USD)
$330,665.93Funder
UK Research and Innovation (UKRI)Principal Investigator
Dr. Simon PowisResearch Location
United KingdomLead Research Institution
University of St AndrewsResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Immunity
Special Interest Tags
N/A
Study Type
Non-Clinical
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Unspecified
Vulnerable Population
Unspecified
Occupations of Interest
Unspecified
Abstract
The immune response to SARS-CoV-2 will comprise both an antibody response (which it is obviously hoped will provide both immediate protection and also prolonged memory) but also crucially a killer T cell response. These cells can seek out and kill virus infected cells, whilst leaving nearby uninfected cells unharmed. Thus they remove the seat of the infection, which antibodies cannot do, and prevent the release of new virus particles. These killer T cells work by recognising small fragments of viral proteins presented to them on immune molecules called HLA class I molecules (HLA-I). Understanding which bits of the virus are being presented by HLA-I to the killer T cells will help inform upon future vaccine design, by incorporating the most targeted bits of the virus into the prospective vaccine. At present this information is not known. We have developed a new method to identify these viral fragments using simple to access blood samples from patients, thus vastly improving on traditional methods which would require a solid lung tissue biopsy. Blood samples contain HLA-I molecules in both a soluble form and also expressed on small vesicles, released from cells in the body, including virus infected cells. Both of these are frequently raised in diseased states where inflammation is present. We will use an antibody that recognises HLA-I molecules to isolate them from patient blood (after first safely inactivating any virus in the blood samples). The small virus fragments are then released from the HLA-I molecules and analysed by a highly sensitive technique called mass spectrometry, which allows us to determine the protein sequence of the virus fragment. Using this technique we can build a picture of which bits of the virus are being seen by these key killer T cells of the immune system. Also, because there are many thousands of different HLA-I molecules present in the human population, our system allows us to identify data which is relevant across a wide spectrum of the population. Our data will allow future vaccine design to incorporate the most relevant bits of the SARS-CoV-2 virus to promote optimal immune responses with, hopefully, long term protection being generated.
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