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. 2023 May 30;15(6):1280. doi: 10.3390/v15061280

Table 3.

Comparison of conventional and surrogate SARS-CoV-2 VNT (the latter in singleplex format and with Wuhan S1 as antigen), using reference and standard sera provided by the European Centre for Disease Prevention and Control (ECDC) and the World Health Organization (WHO).

cVNT sVNT
ID Control Serum/Plasma Inhibition (%) Inhibition (%)
(1:20) (1:20)
EQA A SARS-CoV-2 Abs (Hospitalized patient) 100 * 91
EQA B SARS-CoV-2 Abs (Mild infection) 100 94
EQA C Negative pre-pandemic sera (Other human CoV) 0 0
EQA D SARS-CoV-2 Abs (Hospitalized patient) 100 97
EQA E Acute EBV/CMV sera (Other human CoV) 0 0
EQA F Negative pre-pandemic sera (Other human CoV) 0 0
EQA G SARS-CoV-2 Abs (Mild infection) 100 80
EQA H SARS-CoV-2 Abs (Hospitalized patient) 100 89
JCR 017 SARS-CoV-2 Abs (Standard) 98 80
JCR 018 SARS-CoV-2 Abs (Standard) 92 87
20/136 SARS-CoV-2 Abs (Standard) 100 96
20/140 (20/268) SARS-CoV-2 Abs + NAbs (Lowest Ab levels) 53 54
20/142 (20/268) Negative human sera 6 34
20/144 (20/268) SARS-CoV-2 Abs + NAbs (Low Ab levels) 92 50
20/148 (20/268) SARS-CoV-2 Abs + NAbs (Mid Ab levels) 97 86
20/150 (20/268) SARS-CoV-2 Abs + NAbs (High Ab levels) 100 96

EQA A–H—ECDC’s SARS-CoV-2 serological external quality assessment panel; JCR 017 and 018—ECDC’s SARS-CoV-2 serological standards; * 1:100; Abs—antibodies; NAbs—neutralizing antibodies; SARS-CoV-2—Severe acute respiratory syndrome coronavirus 2; CoV—coronavirus; EBV—Epstein-Barr virus; CMV—Cytomegalovirus; grey—above positivity cut-off (50% (cVNT), 36% (sVNT)).