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Dataset of antibody variable region sequence features inferred from a respiratory syncytial virus fusion protein-specific B cell receptor repertoire induced by natural infection of a healthy adult

Respiratory syncytial virus (RSV) is the primary cause for acute lower respiratory syndrome in children younger than 5 years. Research on B cell repertoires and antibodies binding the RSV fusion protein (RSV F) is of major interest in the development of potential vaccine candidates and therapies. B...

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Autores principales: Schneikart, Gerald, Tavarini, Simona, Sammicheli, Chiara, Torricelli, Giulia, Guidotti, Silvia, D'Oro, Ugo, Finco, Oretta, Bardelli, Monia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666335/
https://www.ncbi.nlm.nih.gov/pubmed/33225034
http://dx.doi.org/10.1016/j.dib.2020.106499
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author Schneikart, Gerald
Tavarini, Simona
Sammicheli, Chiara
Torricelli, Giulia
Guidotti, Silvia
D'Oro, Ugo
Finco, Oretta
Bardelli, Monia
author_facet Schneikart, Gerald
Tavarini, Simona
Sammicheli, Chiara
Torricelli, Giulia
Guidotti, Silvia
D'Oro, Ugo
Finco, Oretta
Bardelli, Monia
author_sort Schneikart, Gerald
collection PubMed
description Respiratory syncytial virus (RSV) is the primary cause for acute lower respiratory syndrome in children younger than 5 years. Research on B cell repertoires and antibodies binding the RSV fusion protein (RSV F) is of major interest in the development of potential vaccine candidates and therapies. B cell receptors (BCRs) which have higher affinities for a specific antigen are preferentially selected for B cell clonal expansion in germinal center reactions. Consequently, antigen-specific BCR repertoires share common features, as for instance preferential variable gene usage, variable region mutation levels or lengths of the heavy chain complementarity-determining region 3. Since RSV repeatedly infects every person throughout life, memory B cells (MBC) expressing RSV F-binding BCRs circulate in the blood of healthy adults. This dataset of BCR variable region sequence features was derived from single cell-sorted RSV F-directed MBCs of a healthy adult blood donor [1]. The dataset was produced with publicly available data analysis software programs and scripts, which facilitates integration or comparison with antibody sequence repertoire data of different individuals derived with the same or comparable data analysis approaches and tools.
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spelling pubmed-76663352020-11-20 Dataset of antibody variable region sequence features inferred from a respiratory syncytial virus fusion protein-specific B cell receptor repertoire induced by natural infection of a healthy adult Schneikart, Gerald Tavarini, Simona Sammicheli, Chiara Torricelli, Giulia Guidotti, Silvia D'Oro, Ugo Finco, Oretta Bardelli, Monia Data Brief Data Article Respiratory syncytial virus (RSV) is the primary cause for acute lower respiratory syndrome in children younger than 5 years. Research on B cell repertoires and antibodies binding the RSV fusion protein (RSV F) is of major interest in the development of potential vaccine candidates and therapies. B cell receptors (BCRs) which have higher affinities for a specific antigen are preferentially selected for B cell clonal expansion in germinal center reactions. Consequently, antigen-specific BCR repertoires share common features, as for instance preferential variable gene usage, variable region mutation levels or lengths of the heavy chain complementarity-determining region 3. Since RSV repeatedly infects every person throughout life, memory B cells (MBC) expressing RSV F-binding BCRs circulate in the blood of healthy adults. This dataset of BCR variable region sequence features was derived from single cell-sorted RSV F-directed MBCs of a healthy adult blood donor [1]. The dataset was produced with publicly available data analysis software programs and scripts, which facilitates integration or comparison with antibody sequence repertoire data of different individuals derived with the same or comparable data analysis approaches and tools. Elsevier 2020-11-04 /pmc/articles/PMC7666335/ /pubmed/33225034 http://dx.doi.org/10.1016/j.dib.2020.106499 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Schneikart, Gerald
Tavarini, Simona
Sammicheli, Chiara
Torricelli, Giulia
Guidotti, Silvia
D'Oro, Ugo
Finco, Oretta
Bardelli, Monia
Dataset of antibody variable region sequence features inferred from a respiratory syncytial virus fusion protein-specific B cell receptor repertoire induced by natural infection of a healthy adult
title Dataset of antibody variable region sequence features inferred from a respiratory syncytial virus fusion protein-specific B cell receptor repertoire induced by natural infection of a healthy adult
title_full Dataset of antibody variable region sequence features inferred from a respiratory syncytial virus fusion protein-specific B cell receptor repertoire induced by natural infection of a healthy adult
title_fullStr Dataset of antibody variable region sequence features inferred from a respiratory syncytial virus fusion protein-specific B cell receptor repertoire induced by natural infection of a healthy adult
title_full_unstemmed Dataset of antibody variable region sequence features inferred from a respiratory syncytial virus fusion protein-specific B cell receptor repertoire induced by natural infection of a healthy adult
title_short Dataset of antibody variable region sequence features inferred from a respiratory syncytial virus fusion protein-specific B cell receptor repertoire induced by natural infection of a healthy adult
title_sort dataset of antibody variable region sequence features inferred from a respiratory syncytial virus fusion protein-specific b cell receptor repertoire induced by natural infection of a healthy adult
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666335/
https://www.ncbi.nlm.nih.gov/pubmed/33225034
http://dx.doi.org/10.1016/j.dib.2020.106499
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