Predicted impact of the viral mutational landscape on the cytotoxic response against SARS-CoV-2.
Ontology highlight
ABSTRACT: The massive assessment of immune evasion due to viral mutations that increase COVID-19 susceptibility can be computationally facilitated. The adaptive cytotoxic T response is critical during primary infection and the generation of long-term protection. Here, potential HLA class I epitopes in the SARS-CoV-2 proteome were predicted for 2,915 human alleles of 71 families using the netMHCIpan EL algorithm. Allele families showed extreme epitopic differences, underscoring genetic variability of protective capacity between humans. Up to 1,222 epitopes were associated with any of the twelve supertypes, that is, allele clusters covering 90% population. Next, from all mutations identified in ~118,000 viral NCBI isolates, those causing significant epitope score reduction were considered epitope esca
SUBMITTER: Foix A
PROVIDER: S-EPMC8830725 | biostudies-literature | 2022 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA