ACE2 inhibition ELISA is an effective surrogate for SARS-CoV-2 live virus neutralisation

Neutralising antibodies are a candidate correlate of protection against SARS-CoV-2, typically they are measured using live virus neutralisation assays, however, these involve high containment work, are technically demanding and can have a long turn-around time. Therefore, surrogate assays are needed to support rapid screening and vaccine trials. Here, we assessed the Meso Scale Discovery (MSD) ACE2 inhibition assay (ACE2i) as a surrogate by comparing it with live virus neutralisation and total anti-spike IgG across ancestral, Delta, and Omicron SARS-CoV-2 spike proteins. Serum from 103 immunocompromised participants in the UK OCTAVE-DUO trial were analysed at baseline and 21 days post-booster. All assays detected significant post-vaccination increases, but micro-neutralisation assay (MNA) and ACE2i showed marked reductions against VoC, particularly Omicron and this was in contrast to IgG assays. The ACE2i assay offers a rapid, scalable, low containment surrogate for neutralisation to support the licensure of new SARS-CoV-2 vaccines and variant monitoring.

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Publication Details

Journal
Vaccine
Published
2025-12-20
DOI
https://doi.org/10.1016/j.vaccine.2025.128123
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
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article

ACE2 inhibition ELISA is an effective surrogate for SARS-CoV-2 live virus neutralisation

Dung Hoang Nguyen, Eleanor Barnes, Tom Tipton, Stéphanie Longet et al.
Vaccine
SARS-CoV-2 and COVID-19 Research
article

ACE2 inhibition ELISA is an effective surrogate for SARS-CoV-2 live virus neutralisation

Dung Hoang Nguyen, Eleanor Barnes, Tom Tipton, Stéphanie Longet, Miles W. Carroll, Stuart Laidlaw
article en

Abstract

Neutralising antibodies are a candidate correlate of protection against SARS-CoV-2, typically they are measured using live virus neutralisation assays, however, these involve high containment work, are technically demanding and can have a long turn-around time. Therefore, surrogate assays are needed to support rapid screening and vaccine trials. Here, we assessed the Meso Scale Discovery (MSD) ACE2 inhibition assay (ACE2i) as a surrogate by comparing it with live virus neutralisation and total anti-spike IgG across ancestral, Delta, and Omicron SARS-CoV-2 spike proteins. Serum from 103 immunocompromised participants in the UK OCTAVE-DUO trial were analysed at baseline and 21 days post-booster. All assays detected significant post-vaccination increases, but micro-neutralisation assay (MNA) and ACE2i showed marked reductions against VoC, particularly Omicron and this was in contrast to IgG assays. The ACE2i assay offers a rapid, scalable, low containment surrogate for neutralisation to support the licensure of new SARS-CoV-2 vaccines and variant monitoring.

VaccineVol. 72
Centre for Human Genetics (GB), University of Oxford (GB), Oxford BioMedica (United Kingdom) (GB)
Openalex Percentile: Top 52%
SARS-CoV-2 and COVID-19 Research
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