Literature DB >> 34224754

Evaluation of a surrogate virus neutralization test for high-throughput serosurveillance of SARS-CoV-2.

Joachim Mariën1, Johan Michiels2, Leo Heyndrickx2, Antoine Nkuba-Ndaye3, Ann Ceulemans2, Koen Bartholomeeusen2, Joule Madinga3, Placide Mbala-Kingebeni3, Veerle Vanlerberghe4, Steve Ahuka-Mundeke3, Lin-Fa Wang5, Kevin K Ariën6.   

Abstract

High-throughput serological tests that can detect neutralizing antibodies against SARS-CoV-2 are desirable for serosurveillance and vaccine efficacy evaluation. Although the conventional neutralization test (cVNT) remains the gold standard to confirm the presence of neutralizing antibodies in sera, the test is too labour-intensive for massive screening programs and less reproducible as live virus and cell culture is involved. Here, we performed an independent evaluation of a commercially available surrogate virus neutralization test (sVNT, GenScript cPass™) that can be done without biosafety level 3 containment in less than 2 hours. When using the cVNT and a Luminex multiplex immunoassay (MIA) as reference, the sVNT obtained a sensitivity of 94% (CI 90-96%) on a panel of 317 immune sera that were obtained from hospitalized and mild COVID-19 cases from Belgium and a sensitivity of 89% (CI 81-93%) on a panel of 184 healthcare workers from the Democratic Republic of Congo. We also found strong antibody titer correlations (rs>0.8) among the different techniques used. In conclusion, our evaluation suggests that the sVNT could be a powerful tool to monitor/detect neutralising antibodies in cohort and population studies. The technique could be especially useful for vaccine evaluation studies in sub-Saharan Africa where the basic infrastructure to perform cVNTs is lacking.
Copyright © 2021. Published by Elsevier B.V.

Entities:  

Keywords:  Luminex; SARS-CoV-2; cPass; neutralizing antibody test; serosurveillance

Year:  2021        PMID: 34224754     DOI: 10.1016/j.jviromet.2021.114228

Source DB:  PubMed          Journal:  J Virol Methods        ISSN: 0166-0934            Impact factor:   2.014


  8 in total

1.  A SARS-CoV-2 Spike Receptor Binding Motif Peptide Induces Anti-Spike Antibodies in Mice andIs Recognized by COVID-19 Patients.

Authors:  Federico Pratesi; Fosca Errante; Lorenzo Pacini; Irina Charlot Peña-Moreno; Sebastian Quiceno; Alfonso Carotenuto; Saidou Balam; Drissa Konaté; Mahamadou M Diakité; Myriam Arévalo-Herrera; Andrey V Kajava; Paolo Rovero; Giampietro Corradin; Paola Migliorini; Anna M Papini; Sócrates Herrera
Journal:  Front Immunol       Date:  2022-05-26       Impact factor: 8.786

2.  Intranasal Delivery of Thermostable Subunit Vaccine for Cross-Reactive Mucosal and Systemic Antibody Responses Against SARS-CoV-2.

Authors:  Khue G Nguyen; Siena M Mantooth; Maura R Vrabel; David A Zaharoff
Journal:  Front Immunol       Date:  2022-05-03       Impact factor: 8.786

3.  Limited Impact of Delta Variant's Mutations on the Effectiveness of Neutralization Conferred by Natural Infection or COVID-19 Vaccines in a Latino Population.

Authors:  Carlos A Sariol; Crisanta Serrano-Collazo; Edwin J Ortiz; Petraleigh Pantoja; Lorna Cruz; Teresa Arana; Dianne Atehortua; Christina Pabon-Carrero; Ana M Espino
Journal:  Viruses       Date:  2021-11-30       Impact factor: 5.048

4.  Adverse reactions and production of neutralizing anti-SARS-CoV-2 antibodies after ChAdOx1 COVID-19 vaccination: A cross-sectional study in a single center.

Authors:  Yeon Jeong Jeong; Youn Jeong Kim; Si Hyun Kim; Jaeeun Yoo; Jaewoong Lee; Seungok Lee; Sang Il Kim
Journal:  J Infect Public Health       Date:  2022-02-17       Impact factor: 7.537

5.  Clinical Utility of Elecsys Anti-SARS-CoV-2 S Assay in COVID-19 Vaccination: An Exploratory Analysis of the mRNA-1273 Phase 1 Trial.

Authors:  Simon Jochum; Imke Kirste; Sayuri Hortsch; Veit Peter Grunert; Holly Legault; Udo Eichenlaub; Basel Kashlan; Rolando Pajon
Journal:  Front Immunol       Date:  2022-01-19       Impact factor: 7.561

6.  Safety and immunogenicity of an inactivated virus particle vaccine for SARS-CoV-2, BIV1-CovIran: findings from double-blind, randomised, placebo-controlled, phase I and II clinical trials among healthy adults.

Authors:  Minoo Mohraz; Mohammadreza Salehi; Payam Tabarsi; Mohsen Abbasi-Kangevari; Seyyed-Hadi Ghamari; Erfan Ghasemi; Maryam Amini Pouya; Negar Rezaei; Naser Ahmadi; Kazem Heidari; Mohammad-Reza Malekpour; Mojtaba Nasiri; Ali Akbar Amirzargar; Sahar Saeedi Moghaddam; Bagher Larijani; Hamed Hosseini
Journal:  BMJ Open       Date:  2022-04-08       Impact factor: 2.692

7.  Limited impact of Delta variant’s mutations in the effectiveness of neutralization conferred by natural infection or COVID-19 vaccines in a Latino population.

Authors:  Carlos A Sariol; Crisanta Serrano-Collazo; Edwin J Ortiz; Petraleigh Pantoja; Lorna Cruz; Teresa Arana; Dianne Atehortua; Christina Pabon-Carrero; Ana M Espino
Journal:  medRxiv       Date:  2021-10-26

8.  Function Is More Reliable than Quantity to Follow Up the Humoral Response to the Receptor-Binding Domain of SARS-CoV-2-Spike Protein after Natural Infection or COVID-19 Vaccination.

Authors:  Carlos A A Sariol; Petraleigh Pantoja; Crisanta Serrano-Collazo; Tiffany Rosa-Arocho; Albersy Armina-Rodríguez; Lorna Cruz; E Taylor Taylor Stone; Teresa Arana; Consuelo Climent; Gerardo Latoni; Dianne Atehortua; Christina Pabon-Carrero; Amelia K K Pinto; James D D Brien; Ana M M Espino
Journal:  Viruses       Date:  2021-09-30       Impact factor: 5.048

  8 in total

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