Measuring SARS-CoV-2 neutralizing antibody activity using pseudotyped and chimeric viruses.
Animals
Antibodies, Monoclonal
/ immunology
Antibodies, Neutralizing
/ analysis
Antibodies, Viral
/ analysis
Betacoronavirus
/ genetics
COVID-19
Cell Line
Chimera
/ genetics
Chlorocebus aethiops
Coronavirus Infections
/ immunology
HEK293 Cells
HIV-1
/ genetics
Humans
Immunoassay
/ methods
Neutralization Tests
/ methods
Pandemics
Pneumonia, Viral
/ immunology
Recombination, Genetic
SARS-CoV-2
Spike Glycoprotein, Coronavirus
/ genetics
Vero Cells
Vesicular stomatitis Indiana virus
/ genetics
Journal
The Journal of experimental medicine
ISSN: 1540-9538
Titre abrégé: J Exp Med
Pays: United States
ID NLM: 2985109R
Informations de publication
Date de publication:
02 11 2020
02 11 2020
Historique:
received:
08
06
2020
revised:
05
07
2020
accepted:
07
07
2020
entrez:
22
7
2020
pubmed:
22
7
2020
medline:
31
7
2020
Statut:
ppublish
Résumé
The emergence of SARS-CoV-2 and the ensuing explosive epidemic of COVID-19 disease has generated a need for assays to rapidly and conveniently measure the antiviral activity of SARS-CoV-2-specific antibodies. Here, we describe a collection of approaches based on SARS-CoV-2 spike-pseudotyped, single-cycle, replication-defective human immunodeficiency virus type-1 (HIV-1), and vesicular stomatitis virus (VSV), as well as a replication-competent VSV/SARS-CoV-2 chimeric virus. While each surrogate virus exhibited subtle differences in the sensitivity with which neutralizing activity was detected, the neutralizing activity of both convalescent plasma and human monoclonal antibodies measured using each virus correlated quantitatively with neutralizing activity measured using an authentic SARS-CoV-2 neutralization assay. The assays described herein are adaptable to high throughput and are useful tools in the evaluation of serologic immunity conferred by vaccination or prior SARS-CoV-2 infection, as well as the potency of convalescent plasma or human monoclonal antibodies.
Identifiants
pubmed: 32692348
pii: 151961
doi: 10.1084/jem.20201181
pmc: PMC7372514
pii:
doi:
Substances chimiques
Antibodies, Monoclonal
0
Antibodies, Neutralizing
0
Antibodies, Viral
0
Spike Glycoprotein, Coronavirus
0
spike protein, SARS-CoV-2
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIAID NIH HHS
ID : T32 AI070084
Pays : United States
Organisme : Howard Hughes Medical Institute
Pays : United States
Organisme : NIAID NIH HHS
ID : P01 AI138938
Pays : United States
Organisme : NIAID NIH HHS
ID : R37 AI064003
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI111825
Pays : United States
Commentaires et corrections
Type : UpdateOf
Informations de copyright
© 2020 Schmidt et al.
Déclaration de conflit d'intérêts
Disclosures: F. Schmidt reported a patent to VSV/SARS-CoV-2 chimeric virus pending. Y. Weisblum reported a patent to patent on VSV/SARS-CoV-2 chimeric virus pending. D.F. Robbiani reported a patent to monoclonal antibodies against SARS-CoV-2 pending. M.C. Nussenzweig reported a patent to anti-SARS-2 antibodies pending, "Rockefeller University," and is an inventor on the anti-SARS-2 antibody patent that has been submitted by the Rockefeller University. P.D. Bieniasz reported a patent to VSV/SARS-CoV-2 patent pending. No other disclosures were reported.
Références
Nature. 2020 Aug;584(7821):437-442
pubmed: 32555388
Nature. 2020 Aug;584(7819):120-124
pubmed: 32454512
J Virol. 2000 Apr;74(8):3548-54
pubmed: 10729129
Emerg Infect Dis. 2016 Oct;22(10):1824-6
pubmed: 27332149
Virology. 1995 Feb 1;206(2):935-44
pubmed: 7531918
N Engl J Med. 2007 Sep 13;357(11):1162-3
pubmed: 17855683
Science. 2020 Jun 12;368(6496):1274-1278
pubmed: 32404477
Elife. 2019 Oct 23;8:
pubmed: 31644426
Science. 2020 Aug 7;369(6504):643-650
pubmed: 32540902
Cell. 2020 Aug 20;182(4):828-842.e16
pubmed: 32645326
Respirology. 2006 Jan;11(1):49-53
pubmed: 16423201
J Clin Invest. 2020 Jun 1;130(6):2757-2765
pubmed: 32254064
Curr Trop Med Rep. 2020;7(2):61-64
pubmed: 32219057
Cell. 2020 Jul 9;182(1):73-84.e16
pubmed: 32425270
Emerg Infect Dis. 2019 Oct;25(10):1868-1877
pubmed: 31423970
Emerg Infect Dis. 2016 Jun;22(6):
pubmed: 27192543
Nature. 2020 Jul;583(7815):290-295
pubmed: 32422645
J Infect Dis. 2006 Mar 15;193(6):792-5
pubmed: 16479513
Nature. 2003 Nov 27;426(6965):450-4
pubmed: 14647384
Sci Transl Med. 2021 Jan 20;13(577):
pubmed: 33288662
Science. 2020 Aug 7;369(6504):731-736
pubmed: 32540900
J Infect Dis. 2018 May 5;217(11):1728-1739
pubmed: 29741740
Epidemiol Infect. 1990 Oct;105(2):435-46
pubmed: 2170159
J Gen Virol. 2020 Aug;101(8):791-797
pubmed: 32430094
Nature. 2020 Aug;584(7819):115-119
pubmed: 32454513
J Virol. 1986 Aug;59(2):284-91
pubmed: 3016298
Cell. 2015 Jan 29;160(3):433-46
pubmed: 25635457
Science. 2020 Aug 21;369(6506):956-963
pubmed: 32540903
Cell Mol Immunol. 2020 Jun;17(6):647-649
pubmed: 32313207
Emerg Microbes Infect. 2020 Dec;9(1):680-686
pubmed: 32207377
Virology. 2007 May 10;361(2):304-15
pubmed: 17210170
Clin Vaccine Immunol. 2010 Jul;17(7):1055-65
pubmed: 20463105
Emerg Infect Dis. 2017 Jul;23(7):1079-1084
pubmed: 28585916
PLoS Biol. 2006 Dec;4(12):e435
pubmed: 17147474
Int Immunol. 2017 Jul 1;29(7):303-310
pubmed: 28472280
J Virol Methods. 2010 Nov;169(2):365-74
pubmed: 20709108
Immunity. 2020 Jul 14;53(1):98-105.e5
pubmed: 32561270
Gene Ther. 2001 Nov;8(21):1665-8
pubmed: 11895005
Viruses. 2020 May 06;12(5):
pubmed: 32384820
Elife. 2018 Aug 07;7:
pubmed: 30084827