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Source: COVID-19 News  Dec 23, 2020  2 years ago
COVID-19 News: Study By University Of Vienna Shockingly Shows Variety Of SARS-CoV-2 Mutations Including A222V And S477N Evade T Cell Immunity!.
COVID-19 News: Study By University Of Vienna Shockingly Shows Variety Of SARS-CoV-2 Mutations Including A222V And S477N Evade T Cell Immunity!.
Source: COVID-19 News  Dec 23, 2020  2 years ago
COVID-19 News:  Austrian researchers from the University of Vienna, Austrian Academy of Sciences, Kaiser Franz Josef Hospital-Vienna and the Medical University of Innsbruck have in a new study alarmingly discovered that the SARS-CoV-2 coronavirus that that is causing the COVID-19 pandemic are undergoing strategic mutations that affect the host immune capacity to recognize and combat the pathogen via T effector cells.

CD8+ T cell immunity to SARS-CoV-2 has been implicated in COVID-19 severity and virus control, though direct evidence has been lacking so far.
In this study the study team identified non-synonymous mutations in MHC-I restricted CD8+ T cell epitopes after deep sequencing of 747 SARS-CoV-2 virus isolates. Mutant peptides exhibited diminished or abrogated MHC-I binding, which was associated with a loss of recognition and functional responses by CD8+ T cells isolated from HLA-matched COVID-19 patients.
The study findings highlight the capacity of SARS-CoV-2 to subvert CD8+ T cell surveillance through escape mutations in MHC-I-restricted viral epitopes. This provides evolutionary evidence for CD8+ T cell immunity controlling SARS-CoV-2 with consequences for COVID-19 vaccine design.
The study findings will have huge implications on the current COVID-19 vaccines and also some of these mutations were found on the current new UK variant called B.1.1.7 or VOC 202012/01 
The study findings were published on a preprint server and are currently being peer reviewed. https://www.biorxiv.org/content/10.1101/2020.12.18.423507v1
The SARS-CoV-2 coronavirus virus elicits a broad spectrum of immune responses, both innate and adaptive. CD8+ cytotoxic T lymphocyte (CTL) responses occur in these patients, in response to the recognition of a number of antigenic epitopes. The CTLs are very important in clearing the infection as they kill the cell infected by the virus.
Typically this action is triggered by the recognition of the viral peptides displayed on the host cell surface, after they are specifically presented by the right human leukocyte antigen (HLA) in order to activate the corresponding CTLs. The HLA group of antigens is produced by the genes encoding the class I major histocompatibility complex (MHCI).
To date, there is much evidence that CTL-control of some RNA viruses prompts the emergence of viral mutations that prevent MHC-1 restricted recognition of viral antigens with subsequent killing by the CTLs.
The study team objective was to understand the effect of SARS-CoV-2 mutations on viral peptide presentation via MHC-I.
The team utilized used deep sequencing methods with the viral genome and bioinformatics to analyze the results. The genomes came from viral isolates from 747 patient samples.
The study team examined 27 CTL epitopes that were shown to be presented by the common subtype HLA-A*02:01, having an allele frequency of 0.29 in Austria, and by the minor subtype HLA-B*40:01 (allele frequency 0.03-0.05 in Austria).
The study team found around 197 mutations that resulted in amino acid substitutions at CTL epitopes, all present at frequencies of 0.02 or more, in around 230 samples!
Importantly the frequencies of 33 of them were between 0.1 and 0.5. Nine mutations had become the default allele in 53 samples from different patients.
As some of the epitopes overlapped, there resulted in about 207 different epitopes. Of these, 27 were on anchoring residues, while auxiliary residues were affected by 14 mutations. Both these types of amino acids are essential for MHC-I peptide presentation.
It was found that multiple variants were found that had emerged independently in different individuals following infection.
The study team looked at fixed mutations in over 145,000 sequences retrieved from the Global Initiative for Sharing All Influenza Data (GISAID) database. This global dataset showed mutations in up to 7.34% of epitopes. Each of the 27 CTL epitopes had 10-11,700 non-synonymous mutations, the average being 807. The low-frequency mutations identified in the current analysis were also found in GISAID as fixed mutations.
An alanine to valine mutation in one epitope was found in over 75 of the sequences analyzed. This particular allele was first reported in June 2020, but is now a defining mutation of the 20A.EU1 subclade. (the mutation is knon as the A222V mutation).This was, however, found to have been present in samples collected from March to April, though at low frequency. This supports the emergence of the same mutation independently in different individuals.

Interestingly, longitudinal sampling from the same patients showed that mutant epitopes arose at a later time period of the infection. This suggests that positive selection pressure due to CTL effector activity was shaping these mutations.
Another subclade 20A.EU2 had the S477N mutation.
Interestingly modeling studies to estimate the binding strength of the peptides in the wildtype and mutant viruses to HLA-A*02:01 and HLA-B*40:01 showed weaker peptide binding to MHC-I.
The study team chose 11 and 17 wildtype and mutant peptides, respectively, that were predicted to have lower binding strength, testing them against recombinant HLA-A*02:01 or HLA-B*40:01 proteins.
The team found that 9/11 wildtype peptides bound to these HLA antigens, stabilizing their structure by strong binding at physiological temperature.
Significantly of the mutants, however, 11 had reduced binding and stabilizing capacity for MHC-I. MEVTPSGTWL is a peptide that binds only to the minor allele HLA-B*40:01 and not to HLA-A*02:01. Other mutants showed weak or no binding, respectively. One of the predicted CTL epitopes was not bound by wildtype or mutant peptides.
The study team then constructed peptide-loaded tetramers of both HLA antigens, for both wildtype and mutant peptides. They found that the latter tetramer type bound with cognate T cells in response to T cell receptor activation at 4°C but not at 37°C. The most likely reason was peptide loss leading to the breakdown of MHC-I structure.
The study team also looked at peptide-specific effector cell responses in peripheral blood mononuclear cells (PBMCs), obtained from COVID-19 patients with either of these alleles. Stimulating HLA-matched PBMCs with these peptides confirmed they were actual T cell epitopes. These virus-stimulated T cells showed interferon-gamma secretion.
However, mutant peptides reduced the immune response, with fewer tetramer-positive CTLs and lower IFN-gamma secretion.
The researchers hypothesized that the SARS-CoV-2 ORF8 protein reduces the expression of MHC-I molecules on the host cell, but more study is required.
The shocking study findings of this current study show that effector T cells may give rise to SARS-CoV-2 mutations which escape immune surveillance.
Corresponding author, Dr Andreas Bergthaler from the CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences-Vienna told Thailand Medical News, “These results imply that mutations found in SARS-CoV-2 isolates promote immune escape from HLA-dependent recognition by CTLs.”
Importantly, the low frequencies of the non-synonymous mutations showed that they had not become fixed, perhaps because of the short periods of infection with this virus compared to HIV or HCV.
At the same time, the fact that there are many separate HLA profiles within the population affects the spread of the virus, since for each individual, there are different sets of CTL epitopes that are triggered by the infection. Thus, different selection pressures were exerted by these varying subsets that shape different viral mutational escapes.
More work is required to understand how single epitope mutations affect virus control.
The study findings highlight the capacity of SARS-CoV-2 to evade adaptive immune responses and provide further evidence for the impact of endogenous CTL responses and their participation in conferring protection in natural and vaccine-induced immunity.
The study team added, “Natural CTL responses in infected individuals seem to be limited to subsets of epitopes, which raises the question whether and how mutations in single epitopes affect virus control.  This may be of particular importance for SARS-CoV-2 subunit vaccines that induce responses against a limited number of epitopes. In summary, our study findings highlight the capacity of SARS-CoV-2 to evade adaptive immune responses and provide further evidence for the impact of endogenous CTL responses and their participation in conferring protection in natural and vaccine-induced immunity.”
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