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10.1016/j.jinf.2021.03.010

http://scihub22266oqcxt.onion/10.1016/j.jinf.2021.03.010
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33753152!7979278!33753152
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suck abstract from ncbi


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pmid33753152      J+Infect 2021 ; 82 (5): 170-177
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  • Validation of a commercially available indirect assay for SARS-CoV-2 neutralising antibodies using a pseudotyped virus assay #MMPMID33753152
  • Murray MJ; McIntosh M; Atkinson C; Mahungu T; Wright E; Chatterton W; Gandy M; Reeves MB
  • J Infect 2021[May]; 82 (5): 170-177 PMID33753152show ga
  • OBJECTIVES: 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. METHODS: 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. RESULTS: The responses observed within the surrogate neutralisation assay demonstrated an extremely strong, highly significant positive correlation with those observed in both pseudotyped virus assays. CONCLUSIONS: 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.
  • |*COVID-19[MESH]
  • |*SARS-CoV-2[MESH]
  • |Antibodies, Neutralizing[MESH]
  • |Antibodies, Viral[MESH]
  • |Enzyme-Linked Immunosorbent Assay[MESH]


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