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In Vitro Analysis of the Effect of SARS-CoV-2 Non-VOC and four Variants of Concern on MHC-Class-I Expression on Calu-3 and Caco-2 Cells †

As the MHC-I-pathway is key to antigen presentation to cytotoxic T-cells and, therefore, recognition by the host adaptive immune system, we hypothesized that SARS-CoV-2 including its Variants of Concern (VOCs), influences MHC-I expression on epithelial cell surfaces as an immune evasion strategy. We...

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Autores principales: Bahlmann, Nora A., Mautner, Lena, Hoyos, Mona, Sallard, Erwan, Berger, Carola, Dangel, Alexandra, Jönsson, Franziska, Fischer, Johannes C., Kreppel, Florian, Zhang, Wenli, Esposito, Irene, Bölke, Edwin, Baiker, Armin, Ehrhardt, Anja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378856/
https://www.ncbi.nlm.nih.gov/pubmed/37510253
http://dx.doi.org/10.3390/genes14071348
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author Bahlmann, Nora A.
Mautner, Lena
Hoyos, Mona
Sallard, Erwan
Berger, Carola
Dangel, Alexandra
Jönsson, Franziska
Fischer, Johannes C.
Kreppel, Florian
Zhang, Wenli
Esposito, Irene
Bölke, Edwin
Baiker, Armin
Ehrhardt, Anja
author_facet Bahlmann, Nora A.
Mautner, Lena
Hoyos, Mona
Sallard, Erwan
Berger, Carola
Dangel, Alexandra
Jönsson, Franziska
Fischer, Johannes C.
Kreppel, Florian
Zhang, Wenli
Esposito, Irene
Bölke, Edwin
Baiker, Armin
Ehrhardt, Anja
author_sort Bahlmann, Nora A.
collection PubMed
description As the MHC-I-pathway is key to antigen presentation to cytotoxic T-cells and, therefore, recognition by the host adaptive immune system, we hypothesized that SARS-CoV-2 including its Variants of Concern (VOCs), influences MHC-I expression on epithelial cell surfaces as an immune evasion strategy. We conducted an in vitro time course experiment with the human airway epithelial cell line Calu-3 and the human colorectal adenocarcinoma cell line Caco-2. Cells were infected with SARS-CoV-2 strains non-VOC/B.1.1, Alpha/B.1.1.7, Beta/B.1.351, Gamma/P.1, and Delta/B.1.617.2. At 2, 24, 48 and 72 h post-infection we performed RT-qPCR to track viral replication. Simultaneously, we performed intracellular staining with a serum of a double-vaccinated healthy adult containing a high amount of spike protein antibody. In flow cytometry experiments, we differentiated between infected (spike protein positive) and bystander (spike protein negative) cells. To compare their HLA expression levels, cells were stained extracellularly with anti-HLA-A-IgG and anti-HLA-B,C-IgG. While HLA-A expression was stable on infected Calu-3 cells for all variants, it increased to different degrees on bystander cells in samples infected with VOCs Beta, Gamma, Delta, or non-VOC over the time course analyzed. In contrast, HLA-A levels were stable in bystander Calu-3 cells in samples infected with the Alpha variant. The upregulation of MHC-I on spike protein negative bystander cells in Calu-3 cell cultures infected with Beta, Gamma, Delta, and partly non-VOC might suggest that infected cells are still capable of secreting inflammatory cytokines like type-I interferons stimulating the MHC-I expression on bystander cells. In comparison, there was no distinct effect on HLA expression level on Caco-2 cells of any of the VOCs or non-VOC. Further investigations of the full range of immune evasion strategies of SARS-CoV-2 variants are warranted.
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spelling pubmed-103788562023-07-29 In Vitro Analysis of the Effect of SARS-CoV-2 Non-VOC and four Variants of Concern on MHC-Class-I Expression on Calu-3 and Caco-2 Cells † Bahlmann, Nora A. Mautner, Lena Hoyos, Mona Sallard, Erwan Berger, Carola Dangel, Alexandra Jönsson, Franziska Fischer, Johannes C. Kreppel, Florian Zhang, Wenli Esposito, Irene Bölke, Edwin Baiker, Armin Ehrhardt, Anja Genes (Basel) Brief Report As the MHC-I-pathway is key to antigen presentation to cytotoxic T-cells and, therefore, recognition by the host adaptive immune system, we hypothesized that SARS-CoV-2 including its Variants of Concern (VOCs), influences MHC-I expression on epithelial cell surfaces as an immune evasion strategy. We conducted an in vitro time course experiment with the human airway epithelial cell line Calu-3 and the human colorectal adenocarcinoma cell line Caco-2. Cells were infected with SARS-CoV-2 strains non-VOC/B.1.1, Alpha/B.1.1.7, Beta/B.1.351, Gamma/P.1, and Delta/B.1.617.2. At 2, 24, 48 and 72 h post-infection we performed RT-qPCR to track viral replication. Simultaneously, we performed intracellular staining with a serum of a double-vaccinated healthy adult containing a high amount of spike protein antibody. In flow cytometry experiments, we differentiated between infected (spike protein positive) and bystander (spike protein negative) cells. To compare their HLA expression levels, cells were stained extracellularly with anti-HLA-A-IgG and anti-HLA-B,C-IgG. While HLA-A expression was stable on infected Calu-3 cells for all variants, it increased to different degrees on bystander cells in samples infected with VOCs Beta, Gamma, Delta, or non-VOC over the time course analyzed. In contrast, HLA-A levels were stable in bystander Calu-3 cells in samples infected with the Alpha variant. The upregulation of MHC-I on spike protein negative bystander cells in Calu-3 cell cultures infected with Beta, Gamma, Delta, and partly non-VOC might suggest that infected cells are still capable of secreting inflammatory cytokines like type-I interferons stimulating the MHC-I expression on bystander cells. In comparison, there was no distinct effect on HLA expression level on Caco-2 cells of any of the VOCs or non-VOC. Further investigations of the full range of immune evasion strategies of SARS-CoV-2 variants are warranted. MDPI 2023-06-26 /pmc/articles/PMC10378856/ /pubmed/37510253 http://dx.doi.org/10.3390/genes14071348 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Bahlmann, Nora A.
Mautner, Lena
Hoyos, Mona
Sallard, Erwan
Berger, Carola
Dangel, Alexandra
Jönsson, Franziska
Fischer, Johannes C.
Kreppel, Florian
Zhang, Wenli
Esposito, Irene
Bölke, Edwin
Baiker, Armin
Ehrhardt, Anja
In Vitro Analysis of the Effect of SARS-CoV-2 Non-VOC and four Variants of Concern on MHC-Class-I Expression on Calu-3 and Caco-2 Cells †
title In Vitro Analysis of the Effect of SARS-CoV-2 Non-VOC and four Variants of Concern on MHC-Class-I Expression on Calu-3 and Caco-2 Cells †
title_full In Vitro Analysis of the Effect of SARS-CoV-2 Non-VOC and four Variants of Concern on MHC-Class-I Expression on Calu-3 and Caco-2 Cells †
title_fullStr In Vitro Analysis of the Effect of SARS-CoV-2 Non-VOC and four Variants of Concern on MHC-Class-I Expression on Calu-3 and Caco-2 Cells †
title_full_unstemmed In Vitro Analysis of the Effect of SARS-CoV-2 Non-VOC and four Variants of Concern on MHC-Class-I Expression on Calu-3 and Caco-2 Cells †
title_short In Vitro Analysis of the Effect of SARS-CoV-2 Non-VOC and four Variants of Concern on MHC-Class-I Expression on Calu-3 and Caco-2 Cells †
title_sort in vitro analysis of the effect of sars-cov-2 non-voc and four variants of concern on mhc-class-i expression on calu-3 and caco-2 cells †
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378856/
https://www.ncbi.nlm.nih.gov/pubmed/37510253
http://dx.doi.org/10.3390/genes14071348
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