Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera

Autores
Oguntuyo, Kasopefoluwa; Stevens, Christian S.; Hung, Chuan Tien; Ikegame, Satoshi; Acklin, Joshua A.; Kowdle, Shreyas S.; Carmichael, Jillian C.; Chiu, Hsin Ping; Azarm, Kristopher D.; Haas, Griffin D.; Amanat, Fatima; Klingler, Jéromine; Baine, Ian; Arinsburg, Suzanne; Bandres, Juan C.; Siddiquey, Mohammed N. A.; Schilke, Robert M.; Woolard, Matthew D.; Zhang, Hongbo; Duty, Andrew J.; Kraus, Thomas A.; Moran, Thomas M.; Tortorella, Domenico; Lim, Jean K.; Gamarnik, Andrea Vanesa; Hioe, Catarina E.; Zolla Pazner, Susan; Ivanov, Stanimir S.; Kamil, Jeremy; Krammer, Florian; Lee, Benhur; Ojeda, Diego Sebastian; González López Ledesma, María Mora; Costa Navarro, Guadalupe Soledad; Pallarés, H. M.; Sanchez, Lautaro Nicolas; Perez, P.; Ostrowsk, M.; Villordo, S. M.; Alvarez, D. E.; Caramelo, J. J.; Carradori, J.; Yanovsky, M. J.
Año de publicación
2021
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The global coronavirus disease 2019 (COVID-19) pandemic has mobilized efforts to develop vaccines and antibody-based therapeutics, including convalescent-phase plasma therapy, that inhibit viral entry by inducing or transferring neutralizing antibodies (nAbs) against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike glycoprotein (CoV2-S). However, rigorous efficacy testing requires extensive screening with live virus under onerous biosafety level 3 (BSL3) conditions, which limits high-throughput screening of patient and vaccine sera. Myriad BSL2-compatible surrogate virus neutralization assays (VNAs) have been developed to overcome this barrier. Yet, there is marked variability between VNAs and how their results are presented, making intergroup comparisons difficult. To address these limitations, we developed a standardized VNA using CoV2-S pseudotyped particles (CoV2pp) based on vesicular stomatitis virus bearing the Renilla luciferase gene in place of its G glyco-protein (VSVDG); this assay can be robustly produced at scale and generate accurate neutralizing titers within 18 h postinfection. Our standardized CoV2pp VNA showed a strong positive correlation with CoV2-S enzyme-linked immunosorbent assay (ELISA) results and live-virus neutralizations in confirmed convalescent-patient sera. Three independent groups subsequently validated our standardized CoV2pp VNA (n . 120). Our data (i) show that absolute 50% inhibitory concentration (absIC50), absIC80, and absIC90 values can be legitimately compared across diverse cohorts, (ii) highlight the substantial but consistent variability in neutralization potency across these cohorts, and (iii) support the use of the absIC80 as a more meaningful metric for assessing the neutralization potency of a vaccine or convalescent-phase sera. Lastly, we used our CoV2pp in a screen to identify ultrapermissive 293T clones that stably express ACE2 or ACE2 plus TMPRSS2. When these are used in combination with our CoV2pp, we can produce CoV2pp sufficient for 150,000 standardized VNAs/week. IMPORTANCE Vaccines and antibody-based therapeutics like convalescent-phase plasma therapy are premised upon inducing or transferring neutralizing antibodies that inhibit SARS-CoV-2 entry into cells. Virus neutralization assays (VNAs) for measuring neutralizing antibody titers (NATs) are an essential part of determining vaccine or therapeutic efficacy. However, such efficacy testing is limited by the inherent dangers of working with the live virus, which requires specialized high-level biocontainment facilities. We there-fore developed a standardized replication-defective pseudotyped particle system that mimics the entry of live SARS-CoV-2. This tool allows for the safe and efficient measurement of NATs, determination of other forms of entry inhibition, and thorough investigation of virus entry mechanisms. Four independent labs across the globe validated our standardized VNA using diverse cohorts. We argue that a standardized and scalable assay is necessary for meaningful comparisons of the myriad of vaccines and antibody-based therapeutics becoming available. Our data provide generalizable metrics for assessing their efficacy.
Fil: Oguntuyo, Kasopefoluwa. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Stevens, Christian S.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Hung, Chuan Tien. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Ikegame, Satoshi. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Acklin, Joshua A.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Kowdle, Shreyas S.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Carmichael, Jillian C.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Chiu, Hsin Ping. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Azarm, Kristopher D.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Haas, Griffin D.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Amanat, Fatima. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Klingler, Jéromine. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Baine, Ian. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Arinsburg, Suzanne. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Bandres, Juan C.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Siddiquey, Mohammed N. A.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Schilke, Robert M.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Woolard, Matthew D.. State University of Louisiana; Estados Unidos
Fil: Zhang, Hongbo. State University of Louisiana; Estados Unidos
Fil: Duty, Andrew J.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Kraus, Thomas A.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Moran, Thomas M.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Tortorella, Domenico. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Lim, Jean K.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Gamarnik, Andrea Vanesa. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Hioe, Catarina E.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Zolla Pazner, Susan. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Ivanov, Stanimir S.. State University of Louisiana; Estados Unidos
Fil: Kamil, Jeremy. State University of Louisiana; Estados Unidos
Fil: Krammer, Florian. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Lee, Benhur. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Ojeda, Diego Sebastian. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas en Retrovirus y Sida. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Biomédicas en Retrovirus y Sida; Argentina
Fil: González López Ledesma, María Mora. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Costa Navarro, Guadalupe Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Pallarés, H. M.. No especifíca;
Fil: Sanchez, Lautaro Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Perez, P.. No especifíca;
Fil: Ostrowsk, M.. No especifíca;
Fil: Villordo, S. M.. No especifíca;
Fil: Alvarez, D. E.. No especifíca;
Fil: Caramelo, J. J.. No especifíca;
Fil: Carradori, J.. No especifíca;
Fil: Yanovsky, M. J.. No especifíca;
Materia
CONVALESCENT-PHASE PLASMA
COVID-19
NEUTRALIZING ANTIBODIES
SARS-COV-2
VIRAL NEUTRALIZATION ASSAY
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/136006

id CONICETDig_c9f8f2aaf414d05c2435594b2a0031e7
oai_identifier_str oai:ri.conicet.gov.ar:11336/136006
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 SeraOguntuyo, KasopefoluwaStevens, Christian S.Hung, Chuan TienIkegame, SatoshiAcklin, Joshua A.Kowdle, Shreyas S.Carmichael, Jillian C.Chiu, Hsin PingAzarm, Kristopher D.Haas, Griffin D.Amanat, FatimaKlingler, JéromineBaine, IanArinsburg, SuzanneBandres, Juan C.Siddiquey, Mohammed N. A.Schilke, Robert M.Woolard, Matthew D.Zhang, HongboDuty, Andrew J.Kraus, Thomas A.Moran, Thomas M.Tortorella, DomenicoLim, Jean K.Gamarnik, Andrea VanesaHioe, Catarina E.Zolla Pazner, SusanIvanov, Stanimir S.Kamil, JeremyKrammer, FlorianLee, BenhurOjeda, Diego SebastianGonzález López Ledesma, María MoraCosta Navarro, Guadalupe SoledadPallarés, H. M.Sanchez, Lautaro NicolasPerez, P.Ostrowsk, M.Villordo, S. M.Alvarez, D. E.Caramelo, J. J.Carradori, J.Yanovsky, M. J.CONVALESCENT-PHASE PLASMACOVID-19NEUTRALIZING ANTIBODIESSARS-COV-2VIRAL NEUTRALIZATION ASSAYhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The global coronavirus disease 2019 (COVID-19) pandemic has mobilized efforts to develop vaccines and antibody-based therapeutics, including convalescent-phase plasma therapy, that inhibit viral entry by inducing or transferring neutralizing antibodies (nAbs) against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike glycoprotein (CoV2-S). However, rigorous efficacy testing requires extensive screening with live virus under onerous biosafety level 3 (BSL3) conditions, which limits high-throughput screening of patient and vaccine sera. Myriad BSL2-compatible surrogate virus neutralization assays (VNAs) have been developed to overcome this barrier. Yet, there is marked variability between VNAs and how their results are presented, making intergroup comparisons difficult. To address these limitations, we developed a standardized VNA using CoV2-S pseudotyped particles (CoV2pp) based on vesicular stomatitis virus bearing the Renilla luciferase gene in place of its G glyco-protein (VSVDG); this assay can be robustly produced at scale and generate accurate neutralizing titers within 18 h postinfection. Our standardized CoV2pp VNA showed a strong positive correlation with CoV2-S enzyme-linked immunosorbent assay (ELISA) results and live-virus neutralizations in confirmed convalescent-patient sera. Three independent groups subsequently validated our standardized CoV2pp VNA (n . 120). Our data (i) show that absolute 50% inhibitory concentration (absIC50), absIC80, and absIC90 values can be legitimately compared across diverse cohorts, (ii) highlight the substantial but consistent variability in neutralization potency across these cohorts, and (iii) support the use of the absIC80 as a more meaningful metric for assessing the neutralization potency of a vaccine or convalescent-phase sera. Lastly, we used our CoV2pp in a screen to identify ultrapermissive 293T clones that stably express ACE2 or ACE2 plus TMPRSS2. When these are used in combination with our CoV2pp, we can produce CoV2pp sufficient for 150,000 standardized VNAs/week. IMPORTANCE Vaccines and antibody-based therapeutics like convalescent-phase plasma therapy are premised upon inducing or transferring neutralizing antibodies that inhibit SARS-CoV-2 entry into cells. Virus neutralization assays (VNAs) for measuring neutralizing antibody titers (NATs) are an essential part of determining vaccine or therapeutic efficacy. However, such efficacy testing is limited by the inherent dangers of working with the live virus, which requires specialized high-level biocontainment facilities. We there-fore developed a standardized replication-defective pseudotyped particle system that mimics the entry of live SARS-CoV-2. This tool allows for the safe and efficient measurement of NATs, determination of other forms of entry inhibition, and thorough investigation of virus entry mechanisms. Four independent labs across the globe validated our standardized VNA using diverse cohorts. We argue that a standardized and scalable assay is necessary for meaningful comparisons of the myriad of vaccines and antibody-based therapeutics becoming available. Our data provide generalizable metrics for assessing their efficacy.Fil: Oguntuyo, Kasopefoluwa. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Stevens, Christian S.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Hung, Chuan Tien. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Ikegame, Satoshi. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Acklin, Joshua A.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Kowdle, Shreyas S.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Carmichael, Jillian C.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Chiu, Hsin Ping. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Azarm, Kristopher D.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Haas, Griffin D.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Amanat, Fatima. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Klingler, Jéromine. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Baine, Ian. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Arinsburg, Suzanne. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Bandres, Juan C.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Siddiquey, Mohammed N. A.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Schilke, Robert M.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Woolard, Matthew D.. State University of Louisiana; Estados UnidosFil: Zhang, Hongbo. State University of Louisiana; Estados UnidosFil: Duty, Andrew J.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Kraus, Thomas A.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Moran, Thomas M.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Tortorella, Domenico. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Lim, Jean K.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Gamarnik, Andrea Vanesa. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Hioe, Catarina E.. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Zolla Pazner, Susan. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Ivanov, Stanimir S.. State University of Louisiana; Estados UnidosFil: Kamil, Jeremy. State University of Louisiana; Estados UnidosFil: Krammer, Florian. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Lee, Benhur. Icahn School of Medicine at Mount Sinai; Estados UnidosFil: Ojeda, Diego Sebastian. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas en Retrovirus y Sida. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Biomédicas en Retrovirus y Sida; ArgentinaFil: González López Ledesma, María Mora. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; ArgentinaFil: Costa Navarro, Guadalupe Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; ArgentinaFil: Pallarés, H. M.. No especifíca;Fil: Sanchez, Lautaro Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; ArgentinaFil: Perez, P.. No especifíca;Fil: Ostrowsk, M.. No especifíca;Fil: Villordo, S. M.. No especifíca;Fil: Alvarez, D. E.. No especifíca;Fil: Caramelo, J. J.. No especifíca;Fil: Carradori, J.. No especifíca;Fil: Yanovsky, M. J.. No especifíca;American Society for Microbiology2021-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/136006Oguntuyo, Kasopefoluwa; Stevens, Christian S.; Hung, Chuan Tien; Ikegame, Satoshi; Acklin, Joshua A.; et al.; Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera; American Society for Microbiology; mBio; 12; 1; 2-2021; 1-232150-7511CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://mbio.asm.org/content/12/1/e02492-20.longinfo:eu-repo/semantics/altIdentifier/doi/10.1128/mbio.02492-20info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:50:41Zoai:ri.conicet.gov.ar:11336/136006instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:50:41.383CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera
title Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera
spellingShingle Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera
Oguntuyo, Kasopefoluwa
CONVALESCENT-PHASE PLASMA
COVID-19
NEUTRALIZING ANTIBODIES
SARS-COV-2
VIRAL NEUTRALIZATION ASSAY
title_short Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera
title_full Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera
title_fullStr Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera
title_full_unstemmed Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera
title_sort Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera
dc.creator.none.fl_str_mv Oguntuyo, Kasopefoluwa
Stevens, Christian S.
Hung, Chuan Tien
Ikegame, Satoshi
Acklin, Joshua A.
Kowdle, Shreyas S.
Carmichael, Jillian C.
Chiu, Hsin Ping
Azarm, Kristopher D.
Haas, Griffin D.
Amanat, Fatima
Klingler, Jéromine
Baine, Ian
Arinsburg, Suzanne
Bandres, Juan C.
Siddiquey, Mohammed N. A.
Schilke, Robert M.
Woolard, Matthew D.
Zhang, Hongbo
Duty, Andrew J.
Kraus, Thomas A.
Moran, Thomas M.
Tortorella, Domenico
Lim, Jean K.
Gamarnik, Andrea Vanesa
Hioe, Catarina E.
Zolla Pazner, Susan
Ivanov, Stanimir S.
Kamil, Jeremy
Krammer, Florian
Lee, Benhur
Ojeda, Diego Sebastian
González López Ledesma, María Mora
Costa Navarro, Guadalupe Soledad
Pallarés, H. M.
Sanchez, Lautaro Nicolas
Perez, P.
Ostrowsk, M.
Villordo, S. M.
Alvarez, D. E.
Caramelo, J. J.
Carradori, J.
Yanovsky, M. J.
author Oguntuyo, Kasopefoluwa
author_facet Oguntuyo, Kasopefoluwa
Stevens, Christian S.
Hung, Chuan Tien
Ikegame, Satoshi
Acklin, Joshua A.
Kowdle, Shreyas S.
Carmichael, Jillian C.
Chiu, Hsin Ping
Azarm, Kristopher D.
Haas, Griffin D.
Amanat, Fatima
Klingler, Jéromine
Baine, Ian
Arinsburg, Suzanne
Bandres, Juan C.
Siddiquey, Mohammed N. A.
Schilke, Robert M.
Woolard, Matthew D.
Zhang, Hongbo
Duty, Andrew J.
Kraus, Thomas A.
Moran, Thomas M.
Tortorella, Domenico
Lim, Jean K.
Gamarnik, Andrea Vanesa
Hioe, Catarina E.
Zolla Pazner, Susan
Ivanov, Stanimir S.
Kamil, Jeremy
Krammer, Florian
Lee, Benhur
Ojeda, Diego Sebastian
González López Ledesma, María Mora
Costa Navarro, Guadalupe Soledad
Pallarés, H. M.
Sanchez, Lautaro Nicolas
Perez, P.
Ostrowsk, M.
Villordo, S. M.
Alvarez, D. E.
Caramelo, J. J.
Carradori, J.
Yanovsky, M. J.
author_role author
author2 Stevens, Christian S.
Hung, Chuan Tien
Ikegame, Satoshi
Acklin, Joshua A.
Kowdle, Shreyas S.
Carmichael, Jillian C.
Chiu, Hsin Ping
Azarm, Kristopher D.
Haas, Griffin D.
Amanat, Fatima
Klingler, Jéromine
Baine, Ian
Arinsburg, Suzanne
Bandres, Juan C.
Siddiquey, Mohammed N. A.
Schilke, Robert M.
Woolard, Matthew D.
Zhang, Hongbo
Duty, Andrew J.
Kraus, Thomas A.
Moran, Thomas M.
Tortorella, Domenico
Lim, Jean K.
Gamarnik, Andrea Vanesa
Hioe, Catarina E.
Zolla Pazner, Susan
Ivanov, Stanimir S.
Kamil, Jeremy
Krammer, Florian
Lee, Benhur
Ojeda, Diego Sebastian
González López Ledesma, María Mora
Costa Navarro, Guadalupe Soledad
Pallarés, H. M.
Sanchez, Lautaro Nicolas
Perez, P.
Ostrowsk, M.
Villordo, S. M.
Alvarez, D. E.
Caramelo, J. J.
Carradori, J.
Yanovsky, M. J.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv CONVALESCENT-PHASE PLASMA
COVID-19
NEUTRALIZING ANTIBODIES
SARS-COV-2
VIRAL NEUTRALIZATION ASSAY
topic CONVALESCENT-PHASE PLASMA
COVID-19
NEUTRALIZING ANTIBODIES
SARS-COV-2
VIRAL NEUTRALIZATION ASSAY
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The global coronavirus disease 2019 (COVID-19) pandemic has mobilized efforts to develop vaccines and antibody-based therapeutics, including convalescent-phase plasma therapy, that inhibit viral entry by inducing or transferring neutralizing antibodies (nAbs) against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike glycoprotein (CoV2-S). However, rigorous efficacy testing requires extensive screening with live virus under onerous biosafety level 3 (BSL3) conditions, which limits high-throughput screening of patient and vaccine sera. Myriad BSL2-compatible surrogate virus neutralization assays (VNAs) have been developed to overcome this barrier. Yet, there is marked variability between VNAs and how their results are presented, making intergroup comparisons difficult. To address these limitations, we developed a standardized VNA using CoV2-S pseudotyped particles (CoV2pp) based on vesicular stomatitis virus bearing the Renilla luciferase gene in place of its G glyco-protein (VSVDG); this assay can be robustly produced at scale and generate accurate neutralizing titers within 18 h postinfection. Our standardized CoV2pp VNA showed a strong positive correlation with CoV2-S enzyme-linked immunosorbent assay (ELISA) results and live-virus neutralizations in confirmed convalescent-patient sera. Three independent groups subsequently validated our standardized CoV2pp VNA (n . 120). Our data (i) show that absolute 50% inhibitory concentration (absIC50), absIC80, and absIC90 values can be legitimately compared across diverse cohorts, (ii) highlight the substantial but consistent variability in neutralization potency across these cohorts, and (iii) support the use of the absIC80 as a more meaningful metric for assessing the neutralization potency of a vaccine or convalescent-phase sera. Lastly, we used our CoV2pp in a screen to identify ultrapermissive 293T clones that stably express ACE2 or ACE2 plus TMPRSS2. When these are used in combination with our CoV2pp, we can produce CoV2pp sufficient for 150,000 standardized VNAs/week. IMPORTANCE Vaccines and antibody-based therapeutics like convalescent-phase plasma therapy are premised upon inducing or transferring neutralizing antibodies that inhibit SARS-CoV-2 entry into cells. Virus neutralization assays (VNAs) for measuring neutralizing antibody titers (NATs) are an essential part of determining vaccine or therapeutic efficacy. However, such efficacy testing is limited by the inherent dangers of working with the live virus, which requires specialized high-level biocontainment facilities. We there-fore developed a standardized replication-defective pseudotyped particle system that mimics the entry of live SARS-CoV-2. This tool allows for the safe and efficient measurement of NATs, determination of other forms of entry inhibition, and thorough investigation of virus entry mechanisms. Four independent labs across the globe validated our standardized VNA using diverse cohorts. We argue that a standardized and scalable assay is necessary for meaningful comparisons of the myriad of vaccines and antibody-based therapeutics becoming available. Our data provide generalizable metrics for assessing their efficacy.
Fil: Oguntuyo, Kasopefoluwa. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Stevens, Christian S.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Hung, Chuan Tien. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Ikegame, Satoshi. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Acklin, Joshua A.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Kowdle, Shreyas S.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Carmichael, Jillian C.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Chiu, Hsin Ping. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Azarm, Kristopher D.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Haas, Griffin D.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Amanat, Fatima. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Klingler, Jéromine. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Baine, Ian. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Arinsburg, Suzanne. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Bandres, Juan C.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Siddiquey, Mohammed N. A.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Schilke, Robert M.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Woolard, Matthew D.. State University of Louisiana; Estados Unidos
Fil: Zhang, Hongbo. State University of Louisiana; Estados Unidos
Fil: Duty, Andrew J.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Kraus, Thomas A.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Moran, Thomas M.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Tortorella, Domenico. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Lim, Jean K.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Gamarnik, Andrea Vanesa. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Hioe, Catarina E.. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Zolla Pazner, Susan. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Ivanov, Stanimir S.. State University of Louisiana; Estados Unidos
Fil: Kamil, Jeremy. State University of Louisiana; Estados Unidos
Fil: Krammer, Florian. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Lee, Benhur. Icahn School of Medicine at Mount Sinai; Estados Unidos
Fil: Ojeda, Diego Sebastian. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas en Retrovirus y Sida. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Biomédicas en Retrovirus y Sida; Argentina
Fil: González López Ledesma, María Mora. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Costa Navarro, Guadalupe Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Pallarés, H. M.. No especifíca;
Fil: Sanchez, Lautaro Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Perez, P.. No especifíca;
Fil: Ostrowsk, M.. No especifíca;
Fil: Villordo, S. M.. No especifíca;
Fil: Alvarez, D. E.. No especifíca;
Fil: Caramelo, J. J.. No especifíca;
Fil: Carradori, J.. No especifíca;
Fil: Yanovsky, M. J.. No especifíca;
description The global coronavirus disease 2019 (COVID-19) pandemic has mobilized efforts to develop vaccines and antibody-based therapeutics, including convalescent-phase plasma therapy, that inhibit viral entry by inducing or transferring neutralizing antibodies (nAbs) against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike glycoprotein (CoV2-S). However, rigorous efficacy testing requires extensive screening with live virus under onerous biosafety level 3 (BSL3) conditions, which limits high-throughput screening of patient and vaccine sera. Myriad BSL2-compatible surrogate virus neutralization assays (VNAs) have been developed to overcome this barrier. Yet, there is marked variability between VNAs and how their results are presented, making intergroup comparisons difficult. To address these limitations, we developed a standardized VNA using CoV2-S pseudotyped particles (CoV2pp) based on vesicular stomatitis virus bearing the Renilla luciferase gene in place of its G glyco-protein (VSVDG); this assay can be robustly produced at scale and generate accurate neutralizing titers within 18 h postinfection. Our standardized CoV2pp VNA showed a strong positive correlation with CoV2-S enzyme-linked immunosorbent assay (ELISA) results and live-virus neutralizations in confirmed convalescent-patient sera. Three independent groups subsequently validated our standardized CoV2pp VNA (n . 120). Our data (i) show that absolute 50% inhibitory concentration (absIC50), absIC80, and absIC90 values can be legitimately compared across diverse cohorts, (ii) highlight the substantial but consistent variability in neutralization potency across these cohorts, and (iii) support the use of the absIC80 as a more meaningful metric for assessing the neutralization potency of a vaccine or convalescent-phase sera. Lastly, we used our CoV2pp in a screen to identify ultrapermissive 293T clones that stably express ACE2 or ACE2 plus TMPRSS2. When these are used in combination with our CoV2pp, we can produce CoV2pp sufficient for 150,000 standardized VNAs/week. IMPORTANCE Vaccines and antibody-based therapeutics like convalescent-phase plasma therapy are premised upon inducing or transferring neutralizing antibodies that inhibit SARS-CoV-2 entry into cells. Virus neutralization assays (VNAs) for measuring neutralizing antibody titers (NATs) are an essential part of determining vaccine or therapeutic efficacy. However, such efficacy testing is limited by the inherent dangers of working with the live virus, which requires specialized high-level biocontainment facilities. We there-fore developed a standardized replication-defective pseudotyped particle system that mimics the entry of live SARS-CoV-2. This tool allows for the safe and efficient measurement of NATs, determination of other forms of entry inhibition, and thorough investigation of virus entry mechanisms. Four independent labs across the globe validated our standardized VNA using diverse cohorts. We argue that a standardized and scalable assay is necessary for meaningful comparisons of the myriad of vaccines and antibody-based therapeutics becoming available. Our data provide generalizable metrics for assessing their efficacy.
publishDate 2021
dc.date.none.fl_str_mv 2021-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/136006
Oguntuyo, Kasopefoluwa; Stevens, Christian S.; Hung, Chuan Tien; Ikegame, Satoshi; Acklin, Joshua A.; et al.; Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera; American Society for Microbiology; mBio; 12; 1; 2-2021; 1-23
2150-7511
CONICET Digital
CONICET
url http://hdl.handle.net/11336/136006
identifier_str_mv Oguntuyo, Kasopefoluwa; Stevens, Christian S.; Hung, Chuan Tien; Ikegame, Satoshi; Acklin, Joshua A.; et al.; Quantifying Absolute Neutralization Titers against SARS-CoV-2 by a Standardized Virus Neutralization Assay Allows for CrossCohort Comparisons of COVID-19 Sera; American Society for Microbiology; mBio; 12; 1; 2-2021; 1-23
2150-7511
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://mbio.asm.org/content/12/1/e02492-20.long
info:eu-repo/semantics/altIdentifier/doi/10.1128/mbio.02492-20
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv American Society for Microbiology
publisher.none.fl_str_mv American Society for Microbiology
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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score 13.13397