A Sequence Homology and Bioinformatic Approach Can Predict Candidate Targets for Immune Responses to SARS-CoV-2
Identifieur interne : 000A44 ( 2020/Analysis ); précédent : 000A43; suivant : 000A45A Sequence Homology and Bioinformatic Approach Can Predict Candidate Targets for Immune Responses to SARS-CoV-2
Auteurs : Alba Grifoni [États-Unis] ; John Sidney [États-Unis] ; Yun Zhang [États-Unis] ; Richard H. Scheuermann [États-Unis] ; Bjoern Peters [États-Unis] ; Alessandro Sette [États-Unis]Source :
- Cell Host & Microbe [ 1931-3128 ] ; 2020.
Descripteurs français
- KwdFr :
- Bases de données de protéines, Biologie informatique, Déterminants antigéniques des lymphocytes B (génétique), Déterminants antigéniques des lymphocytes B (immunologie), Déterminants antigéniques des lymphocytes T (génétique), Déterminants antigéniques des lymphocytes T (immunologie), Humains, Infections à coronavirus (immunologie), Infections à coronavirus (virologie), Pandémies, Pneumopathie virale (immunologie), Pneumopathie virale (virologie), Similitude de séquences.
- MESH :
- génétique : Déterminants antigéniques des lymphocytes B, Déterminants antigéniques des lymphocytes T.
- immunologie : Déterminants antigéniques des lymphocytes B, Déterminants antigéniques des lymphocytes T, Infections à coronavirus, Pneumopathie virale.
- virologie : Infections à coronavirus, Pneumopathie virale.
- Bases de données de protéines, Biologie informatique, Humains, Pandémies, Similitude de séquences.
English descriptors
- KwdEn :
- Betacoronavirus (genetics), Betacoronavirus (immunology), Computational Biology, Coronavirus Infections (immunology), Coronavirus Infections (virology), Databases, Protein, Epitopes, B-Lymphocyte (genetics), Epitopes, B-Lymphocyte (immunology), Epitopes, T-Lymphocyte (genetics), Epitopes, T-Lymphocyte (immunology), Humans, Pandemics, Pneumonia, Viral (immunology), Pneumonia, Viral (virology), Sequence Homology.
- MESH :
- chemical , genetics : Epitopes, B-Lymphocyte, Epitopes, T-Lymphocyte.
- genetics : Betacoronavirus.
- immunology : Betacoronavirus, Coronavirus Infections, Epitopes, B-Lymphocyte, Epitopes, T-Lymphocyte, Pneumonia, Viral.
- virology : Coronavirus Infections, Pneumonia, Viral.
- Computational Biology, Databases, Protein, Humans, Pandemics, Sequence Homology.
Abstract
Effective countermeasures against the recent emergence and rapid expansion of the 2019 novel coronavirus (SARS-CoV-2) require the development of data and tools to understand and monitor its spread and immune responses to it. However, little information is available about the targets of immune responses to SARS-CoV-2. We used the Immune Epitope Database and Analysis Resource (IEDB) to catalog available data related to other coronaviruses. This includes SARS-CoV, which has high sequence similarity to SARS-CoV-2 and is the best-characterized coronavirus in terms of epitope responses. We identified multiple specific regions in SARS-CoV-2 that have high homology to the SARS-CoV virus. Parallel bioinformatic predictions identified
Url:
DOI: 10.1016/j.chom.2020.03.002
PubMed: 32183941
PubMed Central: 7142693
Affiliations:
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PMC:7142693Le document en format XML
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<term>Computational Biology</term>
<term>Coronavirus Infections (immunology)</term>
<term>Coronavirus Infections (virology)</term>
<term>Databases, Protein</term>
<term>Epitopes, B-Lymphocyte (genetics)</term>
<term>Epitopes, B-Lymphocyte (immunology)</term>
<term>Epitopes, T-Lymphocyte (genetics)</term>
<term>Epitopes, T-Lymphocyte (immunology)</term>
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<term>Pandemics</term>
<term>Pneumonia, Viral (immunology)</term>
<term>Pneumonia, Viral (virology)</term>
<term>Sequence Homology</term>
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<term>Biologie informatique</term>
<term>Déterminants antigéniques des lymphocytes B (génétique)</term>
<term>Déterminants antigéniques des lymphocytes B (immunologie)</term>
<term>Déterminants antigéniques des lymphocytes T (génétique)</term>
<term>Déterminants antigéniques des lymphocytes T (immunologie)</term>
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<term>Infections à coronavirus (immunologie)</term>
<term>Infections à coronavirus (virologie)</term>
<term>Pandémies</term>
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<term>Pneumopathie virale (virologie)</term>
<term>Similitude de séquences</term>
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<term>Déterminants antigéniques des lymphocytes T</term>
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<term>Déterminants antigéniques des lymphocytes T</term>
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<term>Pneumopathie virale</term>
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<term>Epitopes, T-Lymphocyte</term>
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<keywords scheme="MESH" qualifier="virologie" xml:lang="fr"><term>Infections à coronavirus</term>
<term>Pneumopathie virale</term>
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<front><div type="abstract" xml:lang="en"><title>Summary</title>
<p>Effective countermeasures against the recent emergence and rapid expansion of the 2019 novel coronavirus (SARS-CoV-2) require the development of data and tools to understand and monitor its spread and immune responses to it. However, little information is available about the targets of immune responses to SARS-CoV-2. We used the Immune Epitope Database and Analysis Resource (IEDB) to catalog available data related to other coronaviruses. This includes SARS-CoV, which has high sequence similarity to SARS-CoV-2 and is the best-characterized coronavirus in terms of epitope responses. We identified multiple specific regions in SARS-CoV-2 that have high homology to the SARS-CoV virus. Parallel bioinformatic predictions identified <italic>a priori</italic>
potential B and T cell epitopes for SARS-CoV-2. The independent identification of the same regions using two approaches reflects the high probability that these regions are promising targets for immune recognition of SARS-CoV-2. These predictions can facilitate effective vaccine design against this virus of high priority.</p>
</div>
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</back>
</TEI>
<affiliations><list><country><li>États-Unis</li>
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<region><li>Californie</li>
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</list>
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</tree>
</affiliations>
</record>
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