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BCG vaccine may generate cross-reactive T cells against SARS-CoV-2: In silico analyses and a hypothesis
The world is facing the rising emergency of SARS-CoV-2. The outbreak of COVID-19 has caused a global public health and economic crisis. Recent epidemiological studies have shown that a possible association of BCG vaccination program with decreased COVID-19-related risks, suggesting that BCG may prov...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7440160/ https://www.ncbi.nlm.nih.gov/pubmed/32863070 http://dx.doi.org/10.1016/j.vaccine.2020.08.045 |
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author | Tomita, Yusuke Sato, Ryo Ikeda, Tokunori Sakagami, Takuro |
author_facet | Tomita, Yusuke Sato, Ryo Ikeda, Tokunori Sakagami, Takuro |
author_sort | Tomita, Yusuke |
collection | PubMed |
description | The world is facing the rising emergency of SARS-CoV-2. The outbreak of COVID-19 has caused a global public health and economic crisis. Recent epidemiological studies have shown that a possible association of BCG vaccination program with decreased COVID-19-related risks, suggesting that BCG may provide protection against COVID-19. Non-specific protection against viral infections is considered as a main mechanism of BCG and clinical trials to determine whether BCG vaccine can protect healthcare workers from the COVID-19 are currently underway. We hypothesized that BCG may carry similar T cell epitopes with SARS-CoV-2 and evaluated the hypothesis by utilizing publicly available database and computer algorithms predicting human leukocyte antigen (HLA) class I‐binding peptides. We found that BCG contains similar 9-amino acid sequences with SARS-CoV-2. These closely-related peptides had moderate to high binding affinity for multiple common HLA class I molecules, suggesting that cross-reactive T cells against SARS-CoV-2 could be generated by BCG vaccination. |
format | Online Article Text |
id | pubmed-7440160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Authors. Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74401602020-08-21 BCG vaccine may generate cross-reactive T cells against SARS-CoV-2: In silico analyses and a hypothesis Tomita, Yusuke Sato, Ryo Ikeda, Tokunori Sakagami, Takuro Vaccine Short Communication The world is facing the rising emergency of SARS-CoV-2. The outbreak of COVID-19 has caused a global public health and economic crisis. Recent epidemiological studies have shown that a possible association of BCG vaccination program with decreased COVID-19-related risks, suggesting that BCG may provide protection against COVID-19. Non-specific protection against viral infections is considered as a main mechanism of BCG and clinical trials to determine whether BCG vaccine can protect healthcare workers from the COVID-19 are currently underway. We hypothesized that BCG may carry similar T cell epitopes with SARS-CoV-2 and evaluated the hypothesis by utilizing publicly available database and computer algorithms predicting human leukocyte antigen (HLA) class I‐binding peptides. We found that BCG contains similar 9-amino acid sequences with SARS-CoV-2. These closely-related peptides had moderate to high binding affinity for multiple common HLA class I molecules, suggesting that cross-reactive T cells against SARS-CoV-2 could be generated by BCG vaccination. The Authors. Published by Elsevier Ltd. 2020-09-22 2020-08-20 /pmc/articles/PMC7440160/ /pubmed/32863070 http://dx.doi.org/10.1016/j.vaccine.2020.08.045 Text en © 2020 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Short Communication Tomita, Yusuke Sato, Ryo Ikeda, Tokunori Sakagami, Takuro BCG vaccine may generate cross-reactive T cells against SARS-CoV-2: In silico analyses and a hypothesis |
title | BCG vaccine may generate cross-reactive T cells against SARS-CoV-2: In silico analyses and a hypothesis |
title_full | BCG vaccine may generate cross-reactive T cells against SARS-CoV-2: In silico analyses and a hypothesis |
title_fullStr | BCG vaccine may generate cross-reactive T cells against SARS-CoV-2: In silico analyses and a hypothesis |
title_full_unstemmed | BCG vaccine may generate cross-reactive T cells against SARS-CoV-2: In silico analyses and a hypothesis |
title_short | BCG vaccine may generate cross-reactive T cells against SARS-CoV-2: In silico analyses and a hypothesis |
title_sort | bcg vaccine may generate cross-reactive t cells against sars-cov-2: in silico analyses and a hypothesis |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7440160/ https://www.ncbi.nlm.nih.gov/pubmed/32863070 http://dx.doi.org/10.1016/j.vaccine.2020.08.045 |
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