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Live Imaging and Quantification of Viral Infection in K18 hACE2 Transgenic Mice Using Reporter-Expressing Recombinant SARS-CoV-2
Published on: November 5, 2021
Immune Profile of SARS-CoV-2 Variants of Concern
Caterina A M La Porta1,2,3, Stefano Zapperi1,4,5
1Center for Complexity and Biosystems, University of Milan, Milan, Italy.
Abstract:
The spread of the current Sars-Cov-2 pandemics leads to the development of mutations that are constantly monitored because they could affect the efficacy of vaccines. Three recently identified mutated strains, known as variants of concern, are rapidly spreading worldwide. Here, we study possible effects of these mutations on the immune response to Sars-Cov-2 infection using NetTepi a computational method based on artificial neural networks that considers binding and stability of peptides obtained by proteasome degradation for widely represented HLA class I alleles present in human populations as well as the T-cell propensity of viral peptides that measures their immune response. Our results show variations in the number of potential highly ranked peptides ranging between 0 and 20% depending on the specific HLA allele. The results can be useful to design more specific vaccines.
Insights
New severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mutations may impact vaccine effectiveness. This study used computational methods to analyze how these mutations affect the immune response to SARS-CoV-2, potentially guiding vaccine design.
Area of Science:
- Immunology
- Virology
- Computational Biology
Background:
- The ongoing SARS-CoV-2 pandemic necessitates monitoring viral mutations due to their potential impact on vaccine efficacy.
- Three rapidly spreading variants of concern (VOCs) have emerged globally, posing a significant public health challenge.
Purpose of the Study:
- To computationally investigate the effects of SARS-CoV-2 mutations on the human immune response.
- To assess how viral peptide binding and stability to human leukocyte antigen (HLA) class I alleles are influenced by these mutations.
Main Methods:
- Utilized NetTepi, a computational tool employing artificial neural networks.
- Analyzed peptide binding and stability to common HLA class I alleles.
- Evaluated the T-cell response propensity of viral peptides.
Main Results:
- Identified variations in the number of highly ranked immunogenic peptides, ranging from 0% to 20% across different HLA alleles.
- Demonstrated that specific mutations can alter the landscape of potential T-cell epitopes.
Conclusions:
- SARS-CoV-2 mutations can significantly modulate the immune response by affecting the presentation of viral peptides to T-cells.
- These findings provide valuable insights for the rational design of next-generation vaccines with improved efficacy against emerging variants.
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