Rapid Quantitative Point-Of-Care Diagnostic Test for Post COVID-19 Vaccination Antibody Monitoring
Serological testing is an important diagnostic support tool in the fight against COVID-19. So far, serological testing has been performed on either lateral flow assays, which perform only qualitatively and can be difficult for the individual to read, or standard laboratory assays, which are time- an...
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| Vydané v: | Microbiology spectrum Ročník 10; číslo 2; s. e0039622 |
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| Hlavní autori: | , , , , , , , , |
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| Jazyk: | English |
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United States
American Society for Microbiology
27.04.2022
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| ISSN: | 2165-0497, 2165-0497 |
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| Abstract | Serological testing is an important diagnostic support tool in the fight against COVID-19. So far, serological testing has been performed on either lateral flow assays, which perform only qualitatively and can be difficult for the individual to read, or standard laboratory assays, which are time- and resource-consuming.
Point-of-care (POC) quantification of antibody responses against SARS-CoV-2 spike protein can enable decentralized monitoring of immune responses after infection or vaccination. We evaluated a novel POC microfluidic cartridge-based device (ViroTrack Sero COVID-19 Total Ab) for quantitative detection of total antibodies against SARS-CoV-2 spike trimeric spike protein compared to standard laboratory chemiluminescence (CLIA)-based tests. Antibody responses of 101 individuals were measured on capillary blood, venous whole blood, plasma, and diluted plasma samples directly on the POC. Results were available within 7 min. As the reference, plasma samples were analyzed on DiaSorin LIAISON XL CLIA analyzer using LIAISON SARS-CoV-2 IgM, LIAISON SARS-CoV-2 S1/S2 IgG, and LIAISON SARS-CoV-2 TrimericS IgG assays. The Spearman rank’s correlation coefficient between ViroTrack Sero COVID-19 Total Ab and LIAISON SARS-CoV-2 S1/S2 IgG and LIAISON SARS-CoV-2 TrimericS IgG assays was found to be 0.83 and 0.89, respectively. ViroTrack Sero COVID-19 Total Ab showed high correlation between the different matrixes. Agreement for determination of samples of >230 binding antibody units (BAU)/mL on POC and CLIA methods is estimated to be around 90%. ViroTrack Sero Covid Total Ab is a rapid and simple-to-use POC test with high sensitivity and correlation of numerical results expressed in BAU/mL compared to those of a commercial CLIA assay.
IMPORTANCE
Serological testing is an important diagnostic support tool in the fight against COVID-19. So far, serological testing has been performed on either lateral flow assays, which perform only qualitatively and can be difficult for the individual to read, or standard laboratory assays, which are time- and resource-consuming. The purpose of the study was to evaluate the performance of a new POC microfluidic cartridge-based device based on immunomagnetic agglutination assay that can provide an accurate numerical quantification of the total antibodies within only 7 min from a single drop of capillary blood. We demonstrated a high level of correlation between the POC and the two CLIA laboratory-based immunoassays from Diasorin, thus allowing a potentially wider use of quantitative serology tests in the COVID-19 pandemic. |
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| AbstractList | Point-of-care (POC) quantification of antibody responses against SARS-CoV-2 spike protein can enable decentralized monitoring of immune responses after infection or vaccination. We evaluated a novel POC microfluidic cartridge-based device (ViroTrack Sero COVID-19 Total Ab) for quantitative detection of total antibodies against SARS-CoV-2 spike trimeric spike protein compared to standard laboratory chemiluminescence (CLIA)-based tests. Antibody responses of 101 individuals were measured on capillary blood, venous whole blood, plasma, and diluted plasma samples directly on the POC. Results were available within 7 min. As the reference, plasma samples were analyzed on DiaSorin LIAISON XL CLIA analyzer using LIAISON SARS-CoV-2 IgM, LIAISON SARS-CoV-2 S1/S2 IgG, and LIAISON SARS-CoV-2 TrimericS IgG assays. The Spearman rank's correlation coefficient between ViroTrack Sero COVID-19 Total Ab and LIAISON SARS-CoV-2 S1/S2 IgG and LIAISON SARS-CoV-2 TrimericS IgG assays was found to be 0.83 and 0.89, respectively. ViroTrack Sero COVID-19 Total Ab showed high correlation between the different matrixes. Agreement for determination of samples of >230 binding antibody units (BAU)/mL on POC and CLIA methods is estimated to be around 90%. ViroTrack Sero Covid Total Ab is a rapid and simple-to-use POC test with high sensitivity and correlation of numerical results expressed in BAU/mL compared to those of a commercial CLIA assay. IMPORTANCE Serological testing is an important diagnostic support tool in the fight against COVID-19. So far, serological testing has been performed on either lateral flow assays, which perform only qualitatively and can be difficult for the individual to read, or standard laboratory assays, which are time- and resource-consuming. The purpose of the study was to evaluate the performance of a new POC microfluidic cartridge-based device based on immunomagnetic agglutination assay that can provide an accurate numerical quantification of the total antibodies within only 7 min from a single drop of capillary blood. We demonstrated a high level of correlation between the POC and the two CLIA laboratory-based immunoassays from Diasorin, thus allowing a potentially wider use of quantitative serology tests in the COVID-19 pandemic.Point-of-care (POC) quantification of antibody responses against SARS-CoV-2 spike protein can enable decentralized monitoring of immune responses after infection or vaccination. We evaluated a novel POC microfluidic cartridge-based device (ViroTrack Sero COVID-19 Total Ab) for quantitative detection of total antibodies against SARS-CoV-2 spike trimeric spike protein compared to standard laboratory chemiluminescence (CLIA)-based tests. Antibody responses of 101 individuals were measured on capillary blood, venous whole blood, plasma, and diluted plasma samples directly on the POC. Results were available within 7 min. As the reference, plasma samples were analyzed on DiaSorin LIAISON XL CLIA analyzer using LIAISON SARS-CoV-2 IgM, LIAISON SARS-CoV-2 S1/S2 IgG, and LIAISON SARS-CoV-2 TrimericS IgG assays. The Spearman rank's correlation coefficient between ViroTrack Sero COVID-19 Total Ab and LIAISON SARS-CoV-2 S1/S2 IgG and LIAISON SARS-CoV-2 TrimericS IgG assays was found to be 0.83 and 0.89, respectively. ViroTrack Sero COVID-19 Total Ab showed high correlation between the different matrixes. Agreement for determination of samples of >230 binding antibody units (BAU)/mL on POC and CLIA methods is estimated to be around 90%. ViroTrack Sero Covid Total Ab is a rapid and simple-to-use POC test with high sensitivity and correlation of numerical results expressed in BAU/mL compared to those of a commercial CLIA assay. IMPORTANCE Serological testing is an important diagnostic support tool in the fight against COVID-19. So far, serological testing has been performed on either lateral flow assays, which perform only qualitatively and can be difficult for the individual to read, or standard laboratory assays, which are time- and resource-consuming. The purpose of the study was to evaluate the performance of a new POC microfluidic cartridge-based device based on immunomagnetic agglutination assay that can provide an accurate numerical quantification of the total antibodies within only 7 min from a single drop of capillary blood. We demonstrated a high level of correlation between the POC and the two CLIA laboratory-based immunoassays from Diasorin, thus allowing a potentially wider use of quantitative serology tests in the COVID-19 pandemic. Serological testing is an important diagnostic support tool in the fight against COVID-19. So far, serological testing has been performed on either lateral flow assays, which perform only qualitatively and can be difficult for the individual to read, or standard laboratory assays, which are time- and resource-consuming. Point-of-care (POC) quantification of antibody responses against SARS-CoV-2 spike protein can enable decentralized monitoring of immune responses after infection or vaccination. We evaluated a novel POC microfluidic cartridge-based device (ViroTrack Sero COVID-19 Total Ab) for quantitative detection of total antibodies against SARS-CoV-2 spike trimeric spike protein compared to standard laboratory chemiluminescence (CLIA)-based tests. Antibody responses of 101 individuals were measured on capillary blood, venous whole blood, plasma, and diluted plasma samples directly on the POC. Results were available within 7 min. As the reference, plasma samples were analyzed on DiaSorin LIAISON XL CLIA analyzer using LIAISON SARS-CoV-2 IgM, LIAISON SARS-CoV-2 S1/S2 IgG, and LIAISON SARS-CoV-2 TrimericS IgG assays. The Spearman rank’s correlation coefficient between ViroTrack Sero COVID-19 Total Ab and LIAISON SARS-CoV-2 S1/S2 IgG and LIAISON SARS-CoV-2 TrimericS IgG assays was found to be 0.83 and 0.89, respectively. ViroTrack Sero COVID-19 Total Ab showed high correlation between the different matrixes. Agreement for determination of samples of >230 binding antibody units (BAU)/mL on POC and CLIA methods is estimated to be around 90%. ViroTrack Sero Covid Total Ab is a rapid and simple-to-use POC test with high sensitivity and correlation of numerical results expressed in BAU/mL compared to those of a commercial CLIA assay. IMPORTANCE Serological testing is an important diagnostic support tool in the fight against COVID-19. So far, serological testing has been performed on either lateral flow assays, which perform only qualitatively and can be difficult for the individual to read, or standard laboratory assays, which are time- and resource-consuming. The purpose of the study was to evaluate the performance of a new POC microfluidic cartridge-based device based on immunomagnetic agglutination assay that can provide an accurate numerical quantification of the total antibodies within only 7 min from a single drop of capillary blood. We demonstrated a high level of correlation between the POC and the two CLIA laboratory-based immunoassays from Diasorin, thus allowing a potentially wider use of quantitative serology tests in the COVID-19 pandemic. Point-of-care (POC) quantification of antibody responses against SARS-CoV-2 spike protein can enable decentralized monitoring of immune responses after infection or vaccination. We evaluated a novel POC microfluidic cartridge-based device (ViroTrack Sero COVID-19 Total Ab) for quantitative detection of total antibodies against SARS-CoV-2 spike trimeric spike protein compared to standard laboratory chemiluminescence (CLIA)-based tests. Antibody responses of 101 individuals were measured on capillary blood, venous whole blood, plasma, and diluted plasma samples directly on the POC. Results were available within 7 min. As the reference, plasma samples were analyzed on DiaSorin LIAISON XL CLIA analyzer using LIAISON SARS-CoV-2 IgM, LIAISON SARS-CoV-2 S1/S2 IgG, and LIAISON SARS-CoV-2 TrimericS IgG assays. The Spearman rank's correlation coefficient between ViroTrack Sero COVID-19 Total Ab and LIAISON SARS-CoV-2 S1/S2 IgG and LIAISON SARS-CoV-2 TrimericS IgG assays was found to be 0.83 and 0.89, respectively. ViroTrack Sero COVID-19 Total Ab showed high correlation between the different matrixes. Agreement for determination of samples of >230 binding antibody units (BAU)/mL on POC and CLIA methods is estimated to be around 90%. ViroTrack Sero Covid Total Ab is a rapid and simple-to-use POC test with high sensitivity and correlation of numerical results expressed in BAU/mL compared to those of a commercial CLIA assay. Serological testing is an important diagnostic support tool in the fight against COVID-19. So far, serological testing has been performed on either lateral flow assays, which perform only qualitatively and can be difficult for the individual to read, or standard laboratory assays, which are time- and resource-consuming. The purpose of the study was to evaluate the performance of a new POC microfluidic cartridge-based device based on immunomagnetic agglutination assay that can provide an accurate numerical quantification of the total antibodies within only 7 min from a single drop of capillary blood. We demonstrated a high level of correlation between the POC and the two CLIA laboratory-based immunoassays from Diasorin, thus allowing a potentially wider use of quantitative serology tests in the COVID-19 pandemic. Point-of-care (POC) quantification of antibody responses against SARS-CoV-2 spike protein can enable decentralized monitoring of immune responses after infection or vaccination. We evaluated a novel POC microfluidic cartridge-based device (ViroTrack Sero COVID-19 Total Ab) for quantitative detection of total antibodies against SARS-CoV-2 spike trimeric spike protein compared to standard laboratory chemiluminescence (CLIA)-based tests. Antibody responses of 101 individuals were measured on capillary blood, venous whole blood, plasma, and diluted plasma samples directly on the POC. Results were available within 7 min. As the reference, plasma samples were analyzed on DiaSorin LIAISON XL CLIA analyzer using LIAISON SARS-CoV-2 IgM, LIAISON SARS-CoV-2 S1/S2 IgG, and LIAISON SARS-CoV-2 TrimericS IgG assays. The Spearman rank’s correlation coefficient between ViroTrack Sero COVID-19 Total Ab and LIAISON SARS-CoV-2 S1/S2 IgG and LIAISON SARS-CoV-2 TrimericS IgG assays was found to be 0.83 and 0.89, respectively. ViroTrack Sero COVID-19 Total Ab showed high correlation between the different matrixes. Agreement for determination of samples of >230 binding antibody units (BAU)/mL on POC and CLIA methods is estimated to be around 90%. ViroTrack Sero Covid Total Ab is a rapid and simple-to-use POC test with high sensitivity and correlation of numerical results expressed in BAU/mL compared to those of a commercial CLIA assay. IMPORTANCE Serological testing is an important diagnostic support tool in the fight against COVID-19. So far, serological testing has been performed on either lateral flow assays, which perform only qualitatively and can be difficult for the individual to read, or standard laboratory assays, which are time- and resource-consuming. The purpose of the study was to evaluate the performance of a new POC microfluidic cartridge-based device based on immunomagnetic agglutination assay that can provide an accurate numerical quantification of the total antibodies within only 7 min from a single drop of capillary blood. We demonstrated a high level of correlation between the POC and the two CLIA laboratory-based immunoassays from Diasorin, thus allowing a potentially wider use of quantitative serology tests in the COVID-19 pandemic. ABSTRACT Point-of-care (POC) quantification of antibody responses against SARS-CoV-2 spike protein can enable decentralized monitoring of immune responses after infection or vaccination. We evaluated a novel POC microfluidic cartridge-based device (ViroTrack Sero COVID-19 Total Ab) for quantitative detection of total antibodies against SARS-CoV-2 spike trimeric spike protein compared to standard laboratory chemiluminescence (CLIA)-based tests. Antibody responses of 101 individuals were measured on capillary blood, venous whole blood, plasma, and diluted plasma samples directly on the POC. Results were available within 7 min. As the reference, plasma samples were analyzed on DiaSorin LIAISON XL CLIA analyzer using LIAISON SARS-CoV-2 IgM, LIAISON SARS-CoV-2 S1/S2 IgG, and LIAISON SARS-CoV-2 TrimericS IgG assays. The Spearman rank’s correlation coefficient between ViroTrack Sero COVID-19 Total Ab and LIAISON SARS-CoV-2 S1/S2 IgG and LIAISON SARS-CoV-2 TrimericS IgG assays was found to be 0.83 and 0.89, respectively. ViroTrack Sero COVID-19 Total Ab showed high correlation between the different matrixes. Agreement for determination of samples of >230 binding antibody units (BAU)/mL on POC and CLIA methods is estimated to be around 90%. ViroTrack Sero Covid Total Ab is a rapid and simple-to-use POC test with high sensitivity and correlation of numerical results expressed in BAU/mL compared to those of a commercial CLIA assay. IMPORTANCE Serological testing is an important diagnostic support tool in the fight against COVID-19. So far, serological testing has been performed on either lateral flow assays, which perform only qualitatively and can be difficult for the individual to read, or standard laboratory assays, which are time- and resource-consuming. The purpose of the study was to evaluate the performance of a new POC microfluidic cartridge-based device based on immunomagnetic agglutination assay that can provide an accurate numerical quantification of the total antibodies within only 7 min from a single drop of capillary blood. We demonstrated a high level of correlation between the POC and the two CLIA laboratory-based immunoassays from Diasorin, thus allowing a potentially wider use of quantitative serology tests in the COVID-19 pandemic. |
| Author | Fock, Jeppe Bade, Melanie Pah, Pearlyn Engsig, Frederik N. Donolato, Marco Moeller, Maria E. Benfield, Thomas Soerensen, Anna Louise Bang, Didi |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35357223$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1101/2021.06.21.21258528 10.3390/diagnostics11040593 10.1093/clinchem/hvaa262 10.1016/bs.aivir.2019.08.002 10.1056/NEJMoa2109072 10.1101/2021.08.19.21262111 10.1093/clinchem/hvaa336 10.1515/cclm-2021-0023 10.1016/S1473-3099(20)30634-4 10.1016/S0140-6736(21)01642-1 10.1016/S0140-6736(21)00502-X 10.1128/JCM.01224-20 10.1093/clinchem/hvaa211 10.1002/jmv.26854 10.1056/NEJMe2028079 10.1021/acsnano.5b02379 10.1038/s41586-020-2852-1 10.1038/s41591-021-01377-8 10.1039/c6cp08749c 10.1101/2020.07.17.20140533 10.1016/S0262-4079(21)00808-3 10.1128/JVI.01828-20 10.12659/MSM.924700 10.1101/2020.09.23.20199604 10.1016/j.vaccine.2020.11.054 10.21873/invivo.12138 10.1128/Spectrum.00247-21 10.1101/2021.02.24.21252368 10.1016/S0140-6736(20)31604-4 10.1016/j.cell.2020.02.058 10.1126/science.abd7728 10.1056/NEJMoa2022483 10.1093/ofid/ofab043 10.1038/srep16145 10.1016/j.ebiom.2020.103101 10.1016/S0140-6736(21)00527-4 10.1128/JCM.02257-20 10.1056/NEJMoa2028436 10.1126/science.abc1227 10.1101/2021.04.27.21256205 10.1136/annrheumdis-2021-220656 |
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| Keywords | SARS-CoV-2 rapid IgG-IgM-IgA combined test point-of-care S protein trimer immunomagnetic agglutination assay vaccination |
| Language | English |
| License | This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license. https://creativecommons.org/licenses/by/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license. |
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| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 The authors declare a conflict of interest. P. Pah, M. Bade, J. Fock, and M. Donolato are employed at Blusense Diagnostics APS and have been part of the developing of ViroTrack Sero COVID-19 Total Ab. This work was supported by BluSense Diagnostics who provided the test kits for the study. |
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| References | e_1_3_2_26_2 e_1_3_2_27_2 Yanny B (e_1_3_2_25_2) 2019; 15 e_1_3_2_28_2 e_1_3_2_29_2 e_1_3_2_41_2 e_1_3_2_40_2 e_1_3_2_20_2 e_1_3_2_43_2 e_1_3_2_21_2 e_1_3_2_42_2 e_1_3_2_22_2 e_1_3_2_23_2 e_1_3_2_24_2 e_1_3_2_9_2 e_1_3_2_15_2 e_1_3_2_38_2 e_1_3_2_8_2 e_1_3_2_16_2 e_1_3_2_37_2 e_1_3_2_7_2 e_1_3_2_17_2 e_1_3_2_6_2 e_1_3_2_18_2 e_1_3_2_39_2 e_1_3_2_19_2 e_1_3_2_30_2 e_1_3_2_32_2 e_1_3_2_10_2 e_1_3_2_31_2 e_1_3_2_5_2 e_1_3_2_11_2 e_1_3_2_34_2 e_1_3_2_4_2 e_1_3_2_12_2 e_1_3_2_33_2 e_1_3_2_3_2 e_1_3_2_13_2 e_1_3_2_36_2 e_1_3_2_2_2 e_1_3_2_14_2 e_1_3_2_35_2 Padoan, A, Bonfante, F, Pagliari, M, Bortolami, A, Negrini, D, Zuin, S, Bozzato, D, Cosma, C, Sciacovelli, L, Plebani, M (B18) 2020; 62 Anderson, EJ, Rouphael, NG, Widge, AT, Jackson, LA, Roberts, PC, Makhene, M, Chappell, JD, Denison, MR, Stevens, LJ, Pruijssers, AJ, McDermott, AB, Flach, B, Lin, BC, Doria-Rose, NA, O'Dell, S, Schmidt, SD, Corbett, KS, Swanson, PA, Padilla, M, Neuzil, KM, Bennett, H, Leav, B, Makowski, M, Albert, J, Cross, K, Edara, VV, Floyd, K, Suthar, MS, Martinez, DR, Baric, R, Buchanan, W, Luke, CJ, Phadke, VK, Rostad, CA, Ledgerwood, JE, Graham, BS, Beigel, JH (B12) 2020; 383 Yanny, B, Konyn, P, Najarian, LM, Mitry, A, Saab, S (B24) 2019; 15 Šimánek, V, Pecen, L, Krátká, Z, Fürst, T, Řezáčková, H, Topolčan, O, Fajfrlík, K, Sedláček, D, Šín, R, Pazdiora, P, Zelená, H, Slouka, D, Kučera, R (B26) 2021; 11 Sadoff, J, leGars, M, Shukarev, G, Heerwegh, D, Truyers, C, de Groot, AM, Stoop, J, Tete, S, van Damme, W, Leroux-Roels, I, Berghmans, P-J, Kimmel, M, van Damme, P, de Hoon, J, Smith, W, Stephenson, KE, Barouch, DH, de Rosa, SC, Cohen, KW, McElrath, J, Cormier, E, Scheper, G, Hendriks, J, Struyf, F, Douoguih, M, van Hoof, J, Schuitemaker, H (B14) 2020 Krammer, F, Simon, V (B1) 2020; 368 Lawton, G (B33) 2021; 250 Jackson, LA, Anderson, EJ, Rouphael, NG, Roberts, PC, Makhene, M, Coler, RN, McCullough, MP, Chappell, JD, Denison, MR, Stevens, LJ, Pruijssers, AJ, McDermott, A, Flach, B, Doria-Rose, NA, Corbett, KS, Morabito, KM, O'Dell, S, Schmidt, SD, Swanson, PA, Padilla, M, Mascola, JR, Neuzil, KM, Bennett, H, Sun, W, Peters, E, Makowski, M, Albert, J, Cross, K, Buchanan, W, Pikaart-Tautges, R, Ledgerwood, JE, Graham, BS, Beigel, JH (B11) 2020; 383 Ainsworth, M, Andersson, M, Auckland, K, Baillie, JK, Barnes, E, Beer, S, Beveridge, A, Bibi, S, Blackwell, L, Borak, M, Bown, A, Brooks, T, Burgess-Brown, NA, Camara, S, Catton, M, Chau, KK, Christott, T, Clutterbuck, E, Coker, J, Cornall, RJ, Cox, S, Crawford-Jones, D, Crook, DW, D'Arcangelo, S, Dejnirattsai, W, Dequaire, JMM, Dimitriadis, S, Dingle, KE, Doherty, G, Dold, C, Dong, T, Dunachie, SJ, Ebner, D, Emmenegger, M, Espinosa, A, Eyre, DW, Fairhead, R, Fassih, S, Feehily, C, Felle, S, Fernandez-Cid, A, Fernandez Mendoza, M, Foord, TH, Fordwoh, T, Fox McKee, D, Frater, J, Gallardo Sanchez, V, Gent, N, Georgiou, D, Groves, CJ (B42) 2020; 20 Shields, AM, Faustini, SE, Kristunas, CA, Cook, AM, Backhouse, C, Dunbar, L, Ebanks, D, Emmanuel, B, Crouch, E, Kroeger, A, Hirschfeld, J, Sharma, P, Jaffery, R, Nowak, S, Gee, S, Drayson, MT, Richter, AG, Dietrich, T, Chapple, IC (B10) 2021 Folegatti, PM, Ewer, KJ, Aley, PK, Angus, B, Becker, S, Belij-Rammerstorfer, S, Bellamy, D, Bibi, S, Bittaye, M, Clutterbuck, EA, Dold, C, Faust, SN, Finn, A, Flaxman, AL, Hallis, B, Heath, P, Jenkin, D, Lazarus, R, Makinson, R, Minassian, AM, Pollock, KM, Ramasamy, M, Robinson, H, Snape, M, Tarrant, R, Voysey, M, Green, C, Douglas, AD, Hill, AVS, Lambe, T, Gilbert, SC, Pollard, AJ, Aboagye, J, Adams, K, Ali, A, Allen, E, Allison, JL, Anslow, R, Arbe-Barnes, EH, Babbage, G, Baillie, K, Baker, M, Baker, N, Baker, P, Baleanu, I, Ballaminut, J, Barnes, E, Barrett, J, Bates, L, Batten, A (B13) 2020; 396 Suhandynata, RT, Hoffman, MA, Huang, D, Tran, JT, Kelner, MJ, Reed, SL, McLawhon, RW, Voss, JE, Nemazee, D, Fitzgerald, RL (B20) 2021; 67 Antunes, P, Watterson, D, Parmvi, M, Burger, R, Boisen, A, Young, P, Cooper, MA, Hansen, MF, Ranzoni, A, Donolato, M (B40) 2015; 5 Bal, A, Pozzetto, B, Trabaud, M-A, Escuret, V, Rabilloud, M, Langlois-Jacques, C, Paul, A, Guibert, N, D'Aubarède-Frieh, C, Massardier-Pilonchery, A, Fabien, N, Goncalves, D, Boibieux, A, Morfin-Sherpa, F, Pitiot, V, Gueyffier, F, Lina, B, Fassier, J-B, Trouillet-Assant, S (B16) 2021; 67 Fock, J, Jonasson, C, Johansson, C, Hansen, MF (B41) 2017; 19 Bonelli, F, Blocki, FA, Bunnell, T, Chu, E, de La O, A, Grenache, DG, Marzucchi, G, Montomoli, E, Okoye, L, Pallavicini, L, Streva, VA, Torelli, A, Wagner, A, Zanin, D, Zierold, C, Wassenberg, JJ (B22) 2021; 59 Feng, S, Phillips, D, White, T, Sayal, H, Aley, PK, Bibi, S, Dold, C, Fuskova, M, Gilbert, SC, Hirsch, I, Humphries, HE, Jepson, B, Kelly, EJ, Plested, E, Shoemaker, K, Thomas, KM, Vekemans, J, Villafana, TL, Lambe, T, Pollard, AJ, Voysey, M, Team, OVT (B29) 2021 Bonelli, F, Sarasini, A, Zierold, C, Calleri, M, Bonetti, A, Vismara, C, Blocki, FA, Pallavicini, L, Chinali, A, Campisi, D, Percivalle, E, DiNapoli, AP, Perno, CF, Baldanti, F (B17) 2020; 58 Wang, F, Kream, RM, Stefano, GB (B7) 2020; 26 Barnes, CO, Jette, CA, Abernathy, ME, Dam, K-MA, Esswein, SR, Gristick, HB, Malyutin, AG, Sharaf, NG, Huey-Tubman, KE, Lee, YE, Robbiani, DF, Nussenzweig, MC, West, APJ, Bjorkman, PJ (B5) 2020; 588 Wajnberg, A, Amanat, F, Firpo, A, Altman, DR, Bailey, MJ, Mansour, M, McMahon, M, Meade, P, Mendu, DR, Muellers, K, Stadlbauer, D, Stone, K, Strohmeier, S, Simon, V, Aberg, J, Reich, DL, Krammer, F, Cordon-Cardo, C (B9) 2020; 370 Sahin, U, Muik, A, Derhovanessian, E, Vogler, I, Kranz, LM, Vormehr, M, Baum, A, Pascal, K, Quandt, J, Maurus, D, Brachtendorf, S, Lörks, V, Sikorski, J, Hilker, R, Becker, D, Eller, A-K, Grützner, J, Boesler, C, Rosenbaum, C, Kühnle, M-C, Luxemburger, U, Kemmer-Brück, A, Langer, D, Bexon, M, Bolte, S, Karikó, K, Palanche, T, Fischer, B, Schultz, A, Shi, P-Y, Fontes-Garfias, C, Perez, JL, Swanson, KA, Loschko, J, Scully, IL, Cutler, M, Kalina, W, Kyratsous, CA, Cooper, D, Dormitzer, PR, Jansen, KU, Türeci, Ö (B15) 2020 Tang, MS, Case, JB, Franks, CE, Chen, RE, Anderson, NW, Henderson, JP, Diamond, MS, Gronowski, AM, Farnsworth, CW (B21) 2020; 66 Mahmoud, SA, Ganesan, S, Naik, S, Bissar, S, Zamil, I, Zaher, WA (B27) 2021 Kristiansen, PA, Page, M, Bernasconi, V, Mattiuzzo, G, Dull, P, Makar, K, Plotkin, S, Knezevic, I (B28) 2021; 397 Shrotri, M, Navaratnam, AMD, Nguyen, V, Byrne, T, Geismar, C, Fragaszy, E, Beale, S, Fong, WLE, Patel, P, Kovar, J, Hayward, AC, Aldridge, RW (B37) 2021; 398 Ura, T, Yamashita, A, Mizuki, N, Okuda, K, Shimada, M (B6) 2021; 39 Tortorici, MA, Veesler, D (B8) 2019; 105 Fenwick, C, Croxatto, A, Coste, AT, Pojer, F, André, C, Pellaton, C, Farina, A, Campos, J, Hacker, D, Lau, K, Bosch, B-J, Gonseth Nussle, S, Bochud, M, D’Acremont, V, Trono, D, Greub, G, Pantaleo, G (B23) 2021; 95 Alter, G, Seder, R (B2) 2020; 383 Morshed, M, Sekirov, I, McLennan, M, Levett, PN, Chahil, N, Mak, A, Carruthers, E, Pidduck, T, Kustra, J, Laley, J, Lee, MK, Chu, K, Burgess, F, Vijh, R, Willis, L, Wada, R, Blancaflor, R, Boraston, S, Hayden, A, Krajden, M (B35) 2021; 8 Perkmann, T, Perkmann-Nagele, N, Koller, T, Mucher, P, Radakovics, A, Marculescu, R, Wolzt, M, Wagner, OF, Binder, CJ, Haslacher, H (B25) 2021; 9 Patel, EU, Bloch, EM, Clarke, W, Hsieh, Y-H, Boon, D, Eby, Y, Fernandez, RE, Baker, OR, Keruly, M, Kirby, CS, Klock, E, Littlefield, K, Miller, J, Schmidt, HA, Sullivan, P, Piwowar-Manning, E, Shrestha, R, Redd, AD, Rothman, RE, Sullivan, D, Shoham, S, Casadevall, A, Quinn, TC, Pekosz, A, Tobian, AAR, Laeyendecker, O (B19) 2021; 59 Khoury, DS, Cromer, D, Reynaldi, A, Schlub, TE, Wheatley, AK, Juno, JA, Subbarao, K, Kent, SJ, Triccas, JA, Davenport, MP (B30) 2021; 27 Moeller, ME, Fock, J, Pah, P, Veras, ADLC, Bade, M, Donolato, M, Israelsen, SB, Eugen-Olsen, J, Benfield, T, Engsig, FN (B38) 2021; 93 Mezger, A, Fock, J, Antunes, P, Østerberg, FW, Boisen, A, Nilsson, M, Hansen, MF, Ahlford, A, Donolato, M (B39) 2015; 9 Walls, AC, Park, Y-J, Tortorici, MA, Wall, A, McGuire, AT, Veesler, D (B4) 2020; 181 Israel, A, Shenhar, Y, Green, I, Merzon, E, Golan-Cohen, A, Schäffer, AA, Ruppin, E, Vinker, S, Magen, E (B36) 2021 Fragkou, PC, Papaevangelou, V, Antoniadou, A, Kavvatha, D, Ploussi, A, Pantazis, N, Sirmpilantze, T, Psarrakis, C, Pournaras, SA, Tsiodras, S, Kelekis, A (B34) 2020; 34 Prendecki, M, Clarke, C, Brown, J, Cox, A, Gleeson, S, Guckian, M, Randell, P, Pria, AD, Lightstone, L, Xu, X-N, Barclay, W, McAdoo, SP, Kelleher, P, Willicombe, M (B3) 2021; 397 Ruddy, JA, Connolly, CM, Boyarsky, BJ, Werbel, WA, Christopher-Stine, L, Garonzik-Wang, J, Segev, DL, Paik, JJ (B31) 2021; 80 Bergwerk, M, Gonen, T, Lustig, Y, Amit, S, Lipsitch, M, Cohen, C, Mandelboim, M, Gal Levin, E, Rubin, C, Indenbaum, V, Tal, I, Zavitan, M, Zuckerman, N, Bar-Chaim, A, Kreiss, Y, Regev-Yochay, G (B32) 2021; 385 |
| References_xml | – ident: e_1_3_2_30_2 doi: 10.1101/2021.06.21.21258528 – ident: e_1_3_2_27_2 doi: 10.3390/diagnostics11040593 – ident: e_1_3_2_21_2 doi: 10.1093/clinchem/hvaa262 – ident: e_1_3_2_9_2 doi: 10.1016/bs.aivir.2019.08.002 – ident: e_1_3_2_33_2 doi: 10.1056/NEJMoa2109072 – ident: e_1_3_2_37_2 doi: 10.1101/2021.08.19.21262111 – ident: e_1_3_2_17_2 doi: 10.1093/clinchem/hvaa336 – ident: e_1_3_2_23_2 doi: 10.1515/cclm-2021-0023 – ident: e_1_3_2_43_2 doi: 10.1016/S1473-3099(20)30634-4 – volume: 15 start-page: 93 year: 2019 ident: e_1_3_2_25_2 article-title: Management approaches to hepatitis B virus vaccination nonresponse publication-title: Gastroenterol Hepatol (NY) – ident: e_1_3_2_38_2 doi: 10.1016/S0140-6736(21)01642-1 – ident: e_1_3_2_4_2 doi: 10.1016/S0140-6736(21)00502-X – ident: e_1_3_2_18_2 doi: 10.1128/JCM.01224-20 – ident: e_1_3_2_22_2 doi: 10.1093/clinchem/hvaa211 – ident: e_1_3_2_39_2 doi: 10.1002/jmv.26854 – ident: e_1_3_2_3_2 doi: 10.1056/NEJMe2028079 – ident: e_1_3_2_40_2 doi: 10.1021/acsnano.5b02379 – ident: e_1_3_2_6_2 doi: 10.1038/s41586-020-2852-1 – ident: e_1_3_2_31_2 doi: 10.1038/s41591-021-01377-8 – ident: e_1_3_2_42_2 doi: 10.1039/c6cp08749c – ident: e_1_3_2_16_2 doi: 10.1101/2020.07.17.20140533 – ident: e_1_3_2_34_2 doi: 10.1016/S0262-4079(21)00808-3 – ident: e_1_3_2_24_2 doi: 10.1128/JVI.01828-20 – ident: e_1_3_2_8_2 doi: 10.12659/MSM.924700 – ident: e_1_3_2_15_2 doi: 10.1101/2020.09.23.20199604 – ident: e_1_3_2_7_2 doi: 10.1016/j.vaccine.2020.11.054 – ident: e_1_3_2_35_2 doi: 10.21873/invivo.12138 – ident: e_1_3_2_26_2 doi: 10.1128/Spectrum.00247-21 – ident: e_1_3_2_11_2 doi: 10.1101/2021.02.24.21252368 – ident: e_1_3_2_14_2 doi: 10.1016/S0140-6736(20)31604-4 – ident: e_1_3_2_5_2 doi: 10.1016/j.cell.2020.02.058 – ident: e_1_3_2_10_2 doi: 10.1126/science.abd7728 – ident: e_1_3_2_12_2 doi: 10.1056/NEJMoa2022483 – ident: e_1_3_2_36_2 doi: 10.1093/ofid/ofab043 – ident: e_1_3_2_41_2 doi: 10.1038/srep16145 – ident: e_1_3_2_19_2 doi: 10.1016/j.ebiom.2020.103101 – ident: e_1_3_2_29_2 doi: 10.1016/S0140-6736(21)00527-4 – ident: e_1_3_2_20_2 doi: 10.1128/JCM.02257-20 – ident: e_1_3_2_13_2 doi: 10.1056/NEJMoa2028436 – ident: e_1_3_2_2_2 doi: 10.1126/science.abc1227 – ident: e_1_3_2_28_2 doi: 10.1101/2021.04.27.21256205 – ident: e_1_3_2_32_2 doi: 10.1136/annrheumdis-2021-220656 – volume: 385 start-page: 1474 year: 2021 end-page: 1484 ident: B32 article-title: Covid-19 breakthrough infections in vaccinated health care workers publication-title: N Engl J Med doi: 10.1056/NEJMoa2109072 – volume: 368 start-page: 1060 year: 2020 end-page: 1061 ident: B1 article-title: Serology assays to manage COVID-19 publication-title: Science doi: 10.1126/science.abc1227 – year: 2021 ident: B27 article-title: Evaluation of serological tests for detecting SARS-CoV-2 antibodies: implementation in assessing post vaccination status publication-title: medRxiv doi: 10.1101/2021.04.27.21256205 – volume: 15 start-page: 93 year: 2019 end-page: 99 ident: B24 article-title: Management approaches to hepatitis B virus vaccination nonresponse publication-title: Gastroenterol Hepatol (NY) – volume: 397 start-page: 1347 year: 2021 end-page: 1348 ident: B28 article-title: WHO International Standard for anti-SARS-CoV-2 immunoglobulin publication-title: Lancet (London, England) doi: 10.1016/S0140-6736(21)00527-4 – volume: 383 start-page: 2427 year: 2020 end-page: 2438 ident: B12 article-title: Safety and immunogenicity of SARS-CoV-2 mRNA-1273 vaccine in older adults publication-title: N Engl J Med doi: 10.1056/NEJMoa2028436 – volume: 67 start-page: 404 year: 2021 end-page: 414 ident: B20 article-title: Commercial serology assays predict neutralization activity against SARS-CoV-2 publication-title: Clin Chem doi: 10.1093/clinchem/hvaa262 – volume: 105 start-page: 93 year: 2019 end-page: 116 ident: B8 article-title: Structural insights into coronavirus entry publication-title: Adv Virus Res doi: 10.1016/bs.aivir.2019.08.002 – volume: 19 start-page: 8802 year: 2017 end-page: 8814 ident: B41 article-title: Characterization of fine particles using optomagnetic measurements publication-title: Phys Chem Chem Phys doi: 10.1039/c6cp08749c – volume: 9 year: 2021 ident: B25 article-title: Anti-spike protein assays to determine SARS-CoV-2 antibody levels: a head-to-head comparison of five quantitative assays publication-title: Microbiol Spectr doi: 10.1128/Spectrum.00247-21 – volume: 80 start-page: 1351 year: 2021 end-page: 1352 ident: B31 article-title: High antibody response to two-dose SARS-CoV-2 messenger RNA vaccination in patients with rheumatic and musculoskeletal diseases publication-title: Ann Rheum Dis doi: 10.1136/annrheumdis-2021-220656 – volume: 11 start-page: 593 year: 2021 ident: B26 article-title: Five commercial immunoassays for SARS-CoV-2 antibody determination and their comparison and correlation with the virus neutralization test publication-title: Diagnostics (Basel, Switzerland) doi: 10.3390/diagnostics11040593 – volume: 8 start-page: ofab043 year: 2021 ident: B35 article-title: Comparative analysis of capillary vs venous blood for serologic detection of SARS-CoV-2 antibodies by RPOC lateral flow tests publication-title: Open Forum Infect Dis doi: 10.1093/ofid/ofab043 – year: 2021 ident: B29 article-title: Correlates of protection against symptomatic and asymptomatic SARS-CoV-2 infection publication-title: medRxiv doi: 10.1101/2021.06.21.21258528 – year: 2020 ident: B15 article-title: Concurrent human antibody and TH1 type T-cell responses elicited by a COVID-19 RNA vaccine publication-title: medRxiv doi: 10.1101/2020.07.17.20140533 – volume: 396 start-page: 467 year: 2020 end-page: 478 ident: B13 article-title: Safety and immunogenicity of the ChAdOx1 nCoV-19 vaccine against SARS-CoV-2: a preliminary report of a phase 1/2, single-blind, randomised controlled trial publication-title: Lancet (London, England) doi: 10.1016/S0140-6736(20)31604-4 – volume: 27 start-page: 1205 year: 2021 end-page: 1211 ident: B30 article-title: Neutralizing antibody levels are highly predictive of immune protection from symptomatic SARS-CoV-2 infection publication-title: Nat Med doi: 10.1038/s41591-021-01377-8 – volume: 66 start-page: 1538 year: 2020 end-page: 1547 ident: B21 article-title: Association between SARS-CoV-2 neutralizing antibodies and commercial serological assays publication-title: Clin Chem doi: 10.1093/clinchem/hvaa211 – year: 2020 ident: B14 article-title: Safety and immunogenicity of the Ad26.COV2.S COVID-19 vaccine candidate: interim results of a phase 1/2a, double-blind, randomized, placebo-controlled trial publication-title: medRxiv doi: 10.1101/2020.09.23.20199604 – volume: 383 start-page: 1782 year: 2020 end-page: 1784 ident: B2 article-title: The power of antibody-based surveillance publication-title: N Engl J Med doi: 10.1056/NEJMe2028079 – volume: 59 start-page: 1463 year: 2021 end-page: 1467 ident: B22 article-title: Evaluation of the automated LIAISON SARS-CoV-2 TrimericS IgG assay for the detection of circulating antibodies publication-title: Clin Chem Lab Med doi: 10.1515/cclm-2021-0023 – volume: 62 start-page: 103101 year: 2020 ident: B18 article-title: Analytical and clinical performances of five immunoassays for the detection of SARS-CoV-2 antibodies in comparison with neutralization activity publication-title: EBioMedicine doi: 10.1016/j.ebiom.2020.103101 – volume: 383 start-page: 1920 year: 2020 end-page: 1931 ident: B11 article-title: An mRNA vaccine against SARS-CoV-2 - preliminary report publication-title: N Engl J Med doi: 10.1056/NEJMoa2022483 – volume: 9 start-page: 7374 year: 2015 end-page: 7382 ident: B39 article-title: Scalable DNA-based magnetic nanoparticle agglutination assay for bacterial detection in patient samples publication-title: ACS Nano doi: 10.1021/acsnano.5b02379 – volume: 181 start-page: 281 year: 2020 end-page: 292.e6 ident: B4 article-title: Structure, function, and antigenicity of the SARS-CoV-2 spike glycoprotein publication-title: Cell doi: 10.1016/j.cell.2020.02.058 – volume: 588 start-page: 682 year: 2020 end-page: 687 ident: B5 article-title: SARS-CoV-2 neutralizing antibody structures inform therapeutic strategies publication-title: Nature doi: 10.1038/s41586-020-2852-1 – volume: 5 start-page: 16145 year: 2015 ident: B40 article-title: Quantification of NS1 dengue biomarker in serum via optomagnetic nanocluster detection publication-title: Sci Rep doi: 10.1038/srep16145 – volume: 20 start-page: 1390 year: 2020 end-page: 1400 ident: B42 article-title: Performance characteristics of five immunoassays for SARS-CoV-2: a head-to-head benchmark comparison publication-title: Lancet Infectious Diseases doi: 10.1016/S1473-3099(20)30634-4 – volume: 58 year: 2020 ident: B17 article-title: Clinical and analytical performance of an automated serological test that identifies S1/S2-neutralizing IgG in COVID-19 patients semiquantitatively publication-title: J Clin Microbiol doi: 10.1128/JCM.01224-20 – volume: 398 start-page: 385 year: 2021 end-page: 387 ident: B37 article-title: Spike-antibody waning after second dose of BNT162b2 or ChAdOx1 publication-title: Lancet doi: 10.1016/S0140-6736(21)01642-1 – year: 2021 ident: B36 article-title: Large-scale study of antibody titer decay following BNT162b2 mRNA vaccine or SARS-CoV-2 infection publication-title: medRxiv doi: 10.1101/2021.08.19.21262111 – volume: 39 start-page: 197 year: 2021 end-page: 201 ident: B6 article-title: New vaccine production platforms used in developing SARS-CoV-2 vaccine candidates publication-title: Vaccine doi: 10.1016/j.vaccine.2020.11.054 – volume: 397 start-page: P1178 year: 2021 end-page: 1181 ident: B3 article-title: Effect of previous SARS-CoV-2 infection on humoral and T-cell responses to single-dose BNT162b2 vaccine publication-title: Lancet (London, England) doi: 10.1016/S0140-6736(21)00502-X – volume: 67 start-page: 742 year: 2021 end-page: 752 ident: B16 article-title: Evaluation of high-throughput SARS-CoV-2 serological assays in a longitudinal cohort of patients with mild COVID-19: clinical sensitivity, specificity, and association with virus neutralization test publication-title: Clin Chem doi: 10.1093/clinchem/hvaa336 – volume: 59 year: 2021 ident: B19 article-title: Comparative performance of five commercially available serologic assays to detect antibodies to SARS-CoV-2 and identify individuals with high neutralizing titers publication-title: J Clin Microbiol doi: 10.1128/JCM.02257-20 – volume: 26 year: 2020 ident: B7 article-title: An evidence based perspective on mRNA-SARS-CoV-2 vaccine development publication-title: Med Sci Monit doi: 10.12659/MSM.924700 – volume: 250 start-page: 8 year: 2021 end-page: 9 ident: B33 article-title: Are booster shots coming? publication-title: New Sci doi: 10.1016/S0262-4079(21)00808-3 – volume: 93 start-page: 3084 year: 2021 end-page: 3091 ident: B38 article-title: Evaluation of commercially available immuno-magnetic agglutination in comparison to enzyme-linked immunosorbent assays for rapid point-of-care diagnostics of COVID-19 publication-title: J Med Virol doi: 10.1002/jmv.26854 – volume: 95 year: 2021 ident: B23 article-title: Changes in SARS-CoV-2 spike versus nucleoprotein antibody responses impact the estimates of infections in population- based seroprevalence studies publication-title: J Virol doi: 10.1128/JVI.01828-20 – year: 2021 ident: B10 article-title: Longitudinal protection following natural SARS-CoV-2 infection and early vaccine responses: insights from a cohort of community based dental health care professionals publication-title: medRxiv doi: 10.1101/2021.02.24.21252368 – volume: 34 start-page: 3039 year: 2020 end-page: 3045 ident: B34 article-title: Preliminary data of a quantitative point of care test for SARS-CoV-2 antibodies from Greece publication-title: In Vivo doi: 10.21873/invivo.12138 – volume: 370 start-page: 1227 year: 2020 end-page: 1230 ident: B9 article-title: Robust neutralizing antibodies to SARS-CoV-2 infection persist for months publication-title: Science doi: 10.1126/science.abd7728 |
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| Snippet | Serological testing is an important diagnostic support tool in the fight against COVID-19. So far, serological testing has been performed on either lateral... Point-of-care (POC) quantification of antibody responses against SARS-CoV-2 spike protein can enable decentralized monitoring of immune responses after... ABSTRACT Point-of-care (POC) quantification of antibody responses against SARS-CoV-2 spike protein can enable decentralized monitoring of immune responses... |
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| SubjectTerms | Antibodies, Viral COVID-19 - diagnosis COVID-19 Vaccines Humans Immunoassay - methods Immunoglobulin G immunomagnetic agglutination assay Pandemics point-of-care Point-of-Care Testing rapid IgG-IgM-IgA combined test Research Article S protein trimer SARS-CoV-2 Sensitivity and Specificity Spike Glycoprotein, Coronavirus Vaccination Vaccines |
| Title | Rapid Quantitative Point-Of-Care Diagnostic Test for Post COVID-19 Vaccination Antibody Monitoring |
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