Identification of similar epitopes between severe acute respiratory syndrome coronavirus-2 and Bacillus Calmette-Guérin: potential for cross-reactive adaptive immunity.

2019‐nCoV BCG Bacillus Calmette–Guérin COVID‐19 SARS‐CoV‐2

Journal

Clinical & translational immunology
ISSN: 2050-0068
Titre abrégé: Clin Transl Immunology
Pays: Australia
ID NLM: 101638268

Informations de publication

Date de publication:
2020
Historique:
received: 20 06 2020
revised: 20 11 2020
accepted: 22 11 2020
entrez: 15 12 2020
pubmed: 16 12 2020
medline: 16 12 2020
Statut: epublish

Résumé

Bacillus Calmette-Guérin (BCG) vaccination has been implicated in protection against severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and as a non-specific immunisation method against the virus. We therefore decided to investigate T-cell and B-cell epitopes within the BCG-Pasteur strain proteome for similarity to immunogenic peptides of SARS-CoV-2. We used NetMHC 4.0 and BepiPred 2.0 epitope prediction methods for the analysis of the BCG-Pasteur proteome to identify similar peptides to established and novel SARS-CoV-2 T-cell and B-cell epitopes. We found 112 BCG MHC-I-restricted T-cell epitopes similar to MHC-I-restricted T-cell SARS-CoV-2 epitopes and 690 BCG B-cell epitopes similar to SARS-CoV-2 B-cell epitopes. The SARS-CoV-2 T-cell epitopes represented 16 SARS-CoV-2 proteins, and the SARS-CoV-2 B-cell epitopes represented 5 SARS-CoV-2 proteins, including the receptor binding domain of the spike glycoprotein. Altogether, our results provide a mechanistic basis for the potential cross-reactive adaptive immunity that may exist between the two microorganisms.

Identifiants

pubmed: 33318797
doi: 10.1002/cti2.1227
pii: CTI21227
pmc: PMC7724920
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e1227

Informations de copyright

© 2020 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Szabolcs Urbán (S)

Department of Nuclear Medicine University of Szeged Szeged Hungary.

Gábor Paragi (G)

MTA-SZTE Biomimetic Systems Research Group University of Szeged Szeged Hungary.
Institute of Physics University of Pecs Pecs Hungary.

Katalin Burián (K)

Department of Medical Microbiology and Immunobiology University of Szeged Szeged Hungary.

Gary R McLean (GR)

Cellular and Molecular Immunology Research Centre London Metropolitan University London UK.
National Heart and Lung Institute Imperial College London London UK.

Dezső P Virok (DP)

Department of Medical Microbiology and Immunobiology University of Szeged Szeged Hungary.

Classifications MeSH