A panel of human neutralizing mAbs targeting SARS-CoV-2 spike at multiple epitopes

The novel highly transmissible human coronavirus SARS-CoV-2 is the causative agent of the COVID-19 pandemic. Thus far, there is no approved therapeutic drug specifically targeting this emerging virus. Here we report the isolation and characterization of a panel of human neutralizing monoclonal antib...

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Autores:
Tipo de recurso:
Article of journal
Fecha de publicación:
2020
Institución:
Universidad de Bogotá Jorge Tadeo Lozano
Repositorio:
Expeditio: repositorio UTadeo
Idioma:
eng
OAI Identifier:
oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/13440
Acceso en línea:
https://www.nature.com/articles/s41467-020-18159-4#article-info
http://hdl.handle.net/20.500.12010/13440
https://doi.org/10.1038/s41467-020-18159-4
Palabra clave:
SARS-CoV-2
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
Rights
License
Abierto (Texto Completo)
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dc.title.spa.fl_str_mv A panel of human neutralizing mAbs targeting SARS-CoV-2 spike at multiple epitopes
title A panel of human neutralizing mAbs targeting SARS-CoV-2 spike at multiple epitopes
spellingShingle A panel of human neutralizing mAbs targeting SARS-CoV-2 spike at multiple epitopes
SARS-CoV-2
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
title_short A panel of human neutralizing mAbs targeting SARS-CoV-2 spike at multiple epitopes
title_full A panel of human neutralizing mAbs targeting SARS-CoV-2 spike at multiple epitopes
title_fullStr A panel of human neutralizing mAbs targeting SARS-CoV-2 spike at multiple epitopes
title_full_unstemmed A panel of human neutralizing mAbs targeting SARS-CoV-2 spike at multiple epitopes
title_sort A panel of human neutralizing mAbs targeting SARS-CoV-2 spike at multiple epitopes
dc.subject.spa.fl_str_mv SARS-CoV-2
topic SARS-CoV-2
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
dc.subject.lemb.spa.fl_str_mv Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
description The novel highly transmissible human coronavirus SARS-CoV-2 is the causative agent of the COVID-19 pandemic. Thus far, there is no approved therapeutic drug specifically targeting this emerging virus. Here we report the isolation and characterization of a panel of human neutralizing monoclonal antibodies targeting the SARS-CoV-2 receptor binding domain (RBD). These antibodies were selected from a phage display library constructed using peripheral circulatory lymphocytes collected from patients at the acute phase of the disease. These neutralizing antibodies are shown to recognize distinct epitopes on the viral spike RBD. A subset of the antibodies exert their inhibitory activity by abrogating binding of the RBD to the human ACE2 receptor. The human monoclonal antibodies described here represent a promising basis for the design of efficient combined post-exposure therapy for SARS-CoV-2 infection.
publishDate 2020
dc.date.accessioned.none.fl_str_mv 2020-09-18T03:20:00Z
dc.date.available.none.fl_str_mv 2020-09-18T03:20:00Z
dc.date.created.none.fl_str_mv 2020-08-27
dc.type.local.spa.fl_str_mv Artículo
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_6501
format http://purl.org/coar/resource_type/c_6501
dc.identifier.issn.spa.fl_str_mv 2041-1723
dc.identifier.other.spa.fl_str_mv https://www.nature.com/articles/s41467-020-18159-4#article-info
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12010/13440
dc.identifier.doi.spa.fl_str_mv https://doi.org/10.1038/s41467-020-18159-4
identifier_str_mv 2041-1723
url https://www.nature.com/articles/s41467-020-18159-4#article-info
http://hdl.handle.net/20.500.12010/13440
https://doi.org/10.1038/s41467-020-18159-4
dc.language.iso.spa.fl_str_mv eng
language eng
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.rights.local.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
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dc.format.extent.spa.fl_str_mv 7 páginas
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Nature Communications
dc.source.spa.fl_str_mv reponame:Expeditio Repositorio Institucional UJTL
instname:Universidad de Bogotá Jorge Tadeo Lozano
instname_str Universidad de Bogotá Jorge Tadeo Lozano
institution Universidad de Bogotá Jorge Tadeo Lozano
reponame_str Expeditio Repositorio Institucional UJTL
collection Expeditio Repositorio Institucional UJTL
bitstream.url.fl_str_mv https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/13440/1/s41467-020-18159-4.pdf
https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/13440/2/license.txt
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spelling 2020-09-18T03:20:00Z2020-09-18T03:20:00Z2020-08-272041-1723https://www.nature.com/articles/s41467-020-18159-4#article-infohttp://hdl.handle.net/20.500.12010/13440https://doi.org/10.1038/s41467-020-18159-47 páginasapplication/pdfengNature Communicationsreponame:Expeditio Repositorio Institucional UJTLinstname:Universidad de Bogotá Jorge Tadeo LozanoSARS-CoV-2Síndrome respiratorio agudo graveCOVID-19SARS-CoV-2CoronavirusA panel of human neutralizing mAbs targeting SARS-CoV-2 spike at multiple epitopesArtículohttp://purl.org/coar/resource_type/c_6501Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2The novel highly transmissible human coronavirus SARS-CoV-2 is the causative agent of the COVID-19 pandemic. Thus far, there is no approved therapeutic drug specifically targeting this emerging virus. Here we report the isolation and characterization of a panel of human neutralizing monoclonal antibodies targeting the SARS-CoV-2 receptor binding domain (RBD). These antibodies were selected from a phage display library constructed using peripheral circulatory lymphocytes collected from patients at the acute phase of the disease. These neutralizing antibodies are shown to recognize distinct epitopes on the viral spike RBD. A subset of the antibodies exert their inhibitory activity by abrogating binding of the RBD to the human ACE2 receptor. The human monoclonal antibodies described here represent a promising basis for the design of efficient combined post-exposure therapy for SARS-CoV-2 infection.Noy-Porat, TalMakdasi, EfiAlcalay, RonMechaly, AdvaLevy, YinonBercovich-Kinori, AdiZauberman, AyeletTamir, HadasYahalom-Ronen, YfatIsraeli, Ma’ayanEpstein, EyalAchdout, HagitMelamed, SharonChitlaru, TheodorWeiss, ShayPeretz, EldarRosen, OsnatParan, NirYitzhaki, ShmuelShapira, Shmuel C.Israely, TomerMazor, OhadRosenfeld, RonitORIGINALs41467-020-18159-4.pdfs41467-020-18159-4.pdfVer documentoapplication/pdf874879https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/13440/1/s41467-020-18159-4.pdf8c7f77214681f3fad96e02418f3dd8a8MD51open accessLICENSElicense.txtlicense.txttext/plain; charset=utf-82938https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/13440/2/license.txtabceeb1c943c50d3343516f9dbfc110fMD52open accessTHUMBNAILs41467-020-18159-4.pdf.jpgs41467-020-18159-4.pdf.jpgIM Thumbnailimage/jpeg15053https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/13440/3/s41467-020-18159-4.pdf.jpgb35fe696222af223bb404722954e8e7dMD53open access20.500.12010/13440oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/134402020-09-17 22:20:00.176open accessRepositorio Institucional - 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