Validation of a commercially available indirect assay for SARS-CoV-2 neutralising antibodies using a pseudotyped virus assay.

Validation of a commercially available indirect assay for SARS-CoV-2 neutralising antibodies using a pseudotyped virus assay.
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DOI:
10.1016/j.jinf.2021.03.010
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发表时间:
2021-05
期刊:
The Journal of infection
影响因子:
--
通讯作者:
Reeves MB
Reeves MB
中科院分区:
其他
文献类型:
--
作者:
Murray MJ;McIntosh M;Atkinson C;Mahungu T;Wright E;Chatterton W;Gandy M;Reeves MB

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An ELISA based cPass assay provides a measure of Spike RBD binding antibodies. Binding in a cPass ELISA correlates strongly with pseudotyped virus neutralisation. ELISA-based surrogate assays provide rapid data on neutralising capacity. To assess whether a commercially available CE-IVD, ELISA-based surrogate neutralisation assay (cPass, Genscript) provides a genuine measure of SARS-CoV-2 neutralisation by human sera, and further to establish whether measuring responses against the RBD of S was a diagnostically useful proxy for responses against the whole S protein. Serum samples from 30 patients were assayed for anti-NP responses, for ‘neutralisation’ by the surrogate neutralisation assay and for neutralisation by SARS-CoV-2 S pseudotyped virus assays utilising two target cell lines. Correlation between assays was measured using linear regression. The responses observed within the surrogate neutralisation assay demonstrated an extremely strong, highly significant positive correlation with those observed in both pseudotyped virus assays. The tested ELISA-based surrogate assay provides an immunologically useful measure of functional immune responses in a much quicker and highly automatable fashion. It also reinforces that detection of anti-RBD neutralising antibodies alone is a powerful measure of the capacity to neutralise viral infection.
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