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A scalable serology solution for profiling humoral immune responses to SARS‐CoV‐2 infection and vaccination

Authors :
Karen Colwill
Yannick Galipeau
Matthew Stuible
Christian Gervais
Corey Arnold
Bhavisha Rathod
Kento T Abe
Jenny H Wang
Adrian Pasculescu
Mariam Maltseva
Lynda Rocheleau
Martin Pelchat
Mahya Fazel‐Zarandi
Mariam Iskilova
Miriam Barrios‐Rodiles
Linda Bennett
Kevin Yau
François Cholette
Christine Mesa
Angel X Li
Aimee Paterson
Michelle A Hladunewich
Pamela J Goodwin
Jeffrey L Wrana
Steven J Drews
Samira Mubareka
Allison J McGeer
John Kim
Marc‐André Langlois
Anne‐Claude Gingras
Yves Durocher
Source :
Clinical & Translational Immunology, Vol 11, Iss 3, Pp n/a-n/a (2022)
Publication Year :
2022
Publisher :
Wiley, 2022.

Abstract

Abstract Objectives Antibody testing against severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has been instrumental in detecting previous exposures and analyzing vaccine‐elicited immune responses. Here, we describe a scalable solution to detect and quantify SARS‐CoV‐2 antibodies, discriminate between natural infection‐ and vaccination‐induced responses, and assess antibody‐mediated inhibition of the spike‐angiotensin converting enzyme 2 (ACE2) interaction. Methods We developed methods and reagents to detect SARS‐CoV‐2 antibodies by enzyme‐linked immunosorbent assay (ELISA). The main assays focus on the parallel detection of immunoglobulin (Ig)Gs against the spike trimer, its receptor binding domain (RBD) and nucleocapsid (N). We automated a surrogate neutralisation (sn)ELISA that measures inhibition of ACE2‐spike or ‐RBD interactions by antibodies. The assays were calibrated to a World Health Organization reference standard. Results Our single‐point IgG‐based ELISAs accurately distinguished non‐infected and infected individuals. For seroprevalence assessment (in a non‐vaccinated cohort), classifying a sample as positive if antibodies were detected for ≥ 2 of the 3 antigens provided the highest specificity. In vaccinated cohorts, increases in anti‐spike and ‐RBD (but not ‐N) antibodies are observed. We present detailed protocols for serum/plasma or dried blood spots analysis performed manually and on automated platforms. The snELISA can be performed automatically at single points, increasing its scalability. Conclusions Measuring antibodies to three viral antigens and identify neutralising antibodies capable of disrupting spike‐ACE2 interactions in high‐throughput enables large‐scale analyses of humoral immune responses to SARS‐CoV‐2 infection and vaccination. The reagents are available to enable scaling up of standardised serological assays, permitting inter‐laboratory data comparison and aggregation.

Details

Language :
English
ISSN :
20500068
Volume :
11
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Clinical & Translational Immunology
Publication Type :
Academic Journal
Accession number :
edsdoj.5e0ee81ad5a14b2c90b3b4fd0393afdc
Document Type :
article
Full Text :
https://doi.org/10.1002/cti2.1380