Homologies between SARS-CoV-2 and allergen proteins may direct T cell-mediated heterologous immune responses

Abstract The outbreak of the new severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is a public health emergency. Asthma does not represent a risk factor for COVID-19 in several published cohorts. We hypothesized that the SARS-CoV-2 proteome contains T cell epitopes, which are potentially...

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Autores principales: Kathrin Balz, Abhinav Kaushik, Meng Chen, Franz Cemic, Vanessa Heger, Harald Renz, Kari Nadeau, Chrysanthi Skevaki
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/d7ea8bc1a9ad40099bef607fbcee3efe
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spelling oai:doaj.org-article:d7ea8bc1a9ad40099bef607fbcee3efe2021-12-02T13:34:46ZHomologies between SARS-CoV-2 and allergen proteins may direct T cell-mediated heterologous immune responses10.1038/s41598-021-84320-82045-2322https://doaj.org/article/d7ea8bc1a9ad40099bef607fbcee3efe2021-02-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-84320-8https://doaj.org/toc/2045-2322Abstract The outbreak of the new severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is a public health emergency. Asthma does not represent a risk factor for COVID-19 in several published cohorts. We hypothesized that the SARS-CoV-2 proteome contains T cell epitopes, which are potentially cross-reactive to allergen epitopes. We aimed at identifying homologous peptide sequences by means of two distinct complementary bioinformatics approaches. Pipeline 1 included prediction of MHC Class I and Class II epitopes contained in the SARS-CoV-2 proteome and allergens along with alignment and elaborate ranking approaches. Pipeline 2 involved alignment of SARS-CoV-2 overlapping peptides with known allergen-derived T cell epitopes. Our results indicate a large number of MHC Class I epitope pairs including known as well as de novo predicted allergen T cell epitopes with high probability for cross-reactivity. Allergen sources, such as Aspergillus fumigatus, Phleum pratense and Dermatophagoides species are of particular interest due to their association with multiple cross-reactive candidate peptides, independently of the applied bioinformatic approach. In contrast, peptides derived from food allergens, as well as MHC class II epitopes did not achieve high in silico ranking and were therefore not further investigated. Our findings warrant further experimental confirmation along with examination of the functional importance of such cross-reactive responses.Kathrin BalzAbhinav KaushikMeng ChenFranz CemicVanessa HegerHarald RenzKari NadeauChrysanthi SkevakiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Kathrin Balz
Abhinav Kaushik
Meng Chen
Franz Cemic
Vanessa Heger
Harald Renz
Kari Nadeau
Chrysanthi Skevaki
Homologies between SARS-CoV-2 and allergen proteins may direct T cell-mediated heterologous immune responses
description Abstract The outbreak of the new severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is a public health emergency. Asthma does not represent a risk factor for COVID-19 in several published cohorts. We hypothesized that the SARS-CoV-2 proteome contains T cell epitopes, which are potentially cross-reactive to allergen epitopes. We aimed at identifying homologous peptide sequences by means of two distinct complementary bioinformatics approaches. Pipeline 1 included prediction of MHC Class I and Class II epitopes contained in the SARS-CoV-2 proteome and allergens along with alignment and elaborate ranking approaches. Pipeline 2 involved alignment of SARS-CoV-2 overlapping peptides with known allergen-derived T cell epitopes. Our results indicate a large number of MHC Class I epitope pairs including known as well as de novo predicted allergen T cell epitopes with high probability for cross-reactivity. Allergen sources, such as Aspergillus fumigatus, Phleum pratense and Dermatophagoides species are of particular interest due to their association with multiple cross-reactive candidate peptides, independently of the applied bioinformatic approach. In contrast, peptides derived from food allergens, as well as MHC class II epitopes did not achieve high in silico ranking and were therefore not further investigated. Our findings warrant further experimental confirmation along with examination of the functional importance of such cross-reactive responses.
format article
author Kathrin Balz
Abhinav Kaushik
Meng Chen
Franz Cemic
Vanessa Heger
Harald Renz
Kari Nadeau
Chrysanthi Skevaki
author_facet Kathrin Balz
Abhinav Kaushik
Meng Chen
Franz Cemic
Vanessa Heger
Harald Renz
Kari Nadeau
Chrysanthi Skevaki
author_sort Kathrin Balz
title Homologies between SARS-CoV-2 and allergen proteins may direct T cell-mediated heterologous immune responses
title_short Homologies between SARS-CoV-2 and allergen proteins may direct T cell-mediated heterologous immune responses
title_full Homologies between SARS-CoV-2 and allergen proteins may direct T cell-mediated heterologous immune responses
title_fullStr Homologies between SARS-CoV-2 and allergen proteins may direct T cell-mediated heterologous immune responses
title_full_unstemmed Homologies between SARS-CoV-2 and allergen proteins may direct T cell-mediated heterologous immune responses
title_sort homologies between sars-cov-2 and allergen proteins may direct t cell-mediated heterologous immune responses
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/d7ea8bc1a9ad40099bef607fbcee3efe
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