Diagnostic performance of the SARS-CoV-2 S1RBD IgG ELISA (immunodiagnostics) for the quantitative detection of SARS-CoV-2 antibodies on dried blood spots
Dried Blood Spots (DBS) are broadly used in SARS-CoV-2 surveillance studies, reporting either the presence or absence of SARS-CoV-2 antibodies. However, quantitative follow-up has become increasingly important to monitor humoral vaccine responses. Therefore, we aimed to evaluate the performance of D...
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creator | Meyers, Eline Coen, Anja De Sutter, An Padalko, Elizaveta Callens, Steven Vandekerckhove, Linos Witkowski, Wojciech Heytens, Stefan Cools, Piet |
description | Dried Blood Spots (DBS) are broadly used in SARS-CoV-2 surveillance studies, reporting either the presence or absence of SARS-CoV-2 antibodies. However, quantitative follow-up has become increasingly important to monitor humoral vaccine responses. Therefore, we aimed to evaluate the performance of DBS for the detection of anti-spike SARS-CoV-2 antibody concentrations using a commercially available assay, reporting in a standardised unitage (International Units/mL; IU/mL).
To assess the sensitivity and specificity of the ImmunoDiagnostics ELISA on serum and DBS for SARS-CoV-2 antibody detection, we analysed 72 paired DBS and serum samples. The SARS-CoV-2 51 IgG ELISA kit (EUROIMMUN) on serum was used as the reference method. We performed a statistical assessment to optimise the cutoff value for DBS and serum and assessed the correlation between DBS and serum antibody concentrations.
We found that anti-spike SARS-CoV-2 antibody concentrations detected in DBS are highly correlated to those detected in paired serum (Pearson correlation 0.98; p-value < 0.0001), allowing to assess serum antibody concentration using DBS. The optimal cut-off for antibody detection on DBS was found to be 26 IU/mL, with 98.1% sensitivity and 100% specificity. For serum, the optimal cut-off was 14 IU/mL, with 100% sensitivity and 100% specificity.
Therefore, we conclude that the ImmunoDiagnostics ELISA kit has optimal performance in the detection of SARS-CoV-2 antibodies on both DBS and serum. This makes DBS ideal for large-scale follow-up of humoral SARS-CoV-2 immune responses, as it is an easy but valuable sampling method for quantification of SARS-CoV-2 antibodies, compared to serum. |
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To assess the sensitivity and specificity of the ImmunoDiagnostics ELISA on serum and DBS for SARS-CoV-2 antibody detection, we analysed 72 paired DBS and serum samples. The SARS-CoV-2 51 IgG ELISA kit (EUROIMMUN) on serum was used as the reference method. We performed a statistical assessment to optimise the cutoff value for DBS and serum and assessed the correlation between DBS and serum antibody concentrations.
We found that anti-spike SARS-CoV-2 antibody concentrations detected in DBS are highly correlated to those detected in paired serum (Pearson correlation 0.98; p-value < 0.0001), allowing to assess serum antibody concentration using DBS. The optimal cut-off for antibody detection on DBS was found to be 26 IU/mL, with 98.1% sensitivity and 100% specificity. For serum, the optimal cut-off was 14 IU/mL, with 100% sensitivity and 100% specificity.
Therefore, we conclude that the ImmunoDiagnostics ELISA kit has optimal performance in the detection of SARS-CoV-2 antibodies on both DBS and serum. This makes DBS ideal for large-scale follow-up of humoral SARS-CoV-2 immune responses, as it is an easy but valuable sampling method for quantification of SARS-CoV-2 antibodies, compared to serum.</description><identifier>ISSN: 1386-6532</identifier><identifier>ISSN: 1873-5967</identifier><language>eng</language><subject>Dried blood spots (DBS) ; Enzyme-linked immunosorbent assay (ELISA) ; Infectious Diseases ; International Units/mL ; Medicine and Health Sciences ; SARS-CoV-2 ; Serology ; Serosurveillance ; Vaccination ; Virology</subject><creationdate>2022</creationdate><rights>Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Public License (CC BY-NC-ND 4.0) info:eu-repo/semantics/openAccess</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,315,776,780,4010,27837</link.rule.ids></links><search><creatorcontrib>Meyers, Eline</creatorcontrib><creatorcontrib>Coen, Anja</creatorcontrib><creatorcontrib>De Sutter, An</creatorcontrib><creatorcontrib>Padalko, Elizaveta</creatorcontrib><creatorcontrib>Callens, Steven</creatorcontrib><creatorcontrib>Vandekerckhove, Linos</creatorcontrib><creatorcontrib>Witkowski, Wojciech</creatorcontrib><creatorcontrib>Heytens, Stefan</creatorcontrib><creatorcontrib>Cools, Piet</creatorcontrib><title>Diagnostic performance of the SARS-CoV-2 S1RBD IgG ELISA (immunodiagnostics) for the quantitative detection of SARS-CoV-2 antibodies on dried blood spots</title><description>Dried Blood Spots (DBS) are broadly used in SARS-CoV-2 surveillance studies, reporting either the presence or absence of SARS-CoV-2 antibodies. However, quantitative follow-up has become increasingly important to monitor humoral vaccine responses. Therefore, we aimed to evaluate the performance of DBS for the detection of anti-spike SARS-CoV-2 antibody concentrations using a commercially available assay, reporting in a standardised unitage (International Units/mL; IU/mL).
To assess the sensitivity and specificity of the ImmunoDiagnostics ELISA on serum and DBS for SARS-CoV-2 antibody detection, we analysed 72 paired DBS and serum samples. The SARS-CoV-2 51 IgG ELISA kit (EUROIMMUN) on serum was used as the reference method. We performed a statistical assessment to optimise the cutoff value for DBS and serum and assessed the correlation between DBS and serum antibody concentrations.
We found that anti-spike SARS-CoV-2 antibody concentrations detected in DBS are highly correlated to those detected in paired serum (Pearson correlation 0.98; p-value < 0.0001), allowing to assess serum antibody concentration using DBS. The optimal cut-off for antibody detection on DBS was found to be 26 IU/mL, with 98.1% sensitivity and 100% specificity. For serum, the optimal cut-off was 14 IU/mL, with 100% sensitivity and 100% specificity.
Therefore, we conclude that the ImmunoDiagnostics ELISA kit has optimal performance in the detection of SARS-CoV-2 antibodies on both DBS and serum. This makes DBS ideal for large-scale follow-up of humoral SARS-CoV-2 immune responses, as it is an easy but valuable sampling method for quantification of SARS-CoV-2 antibodies, compared to serum.</description><subject>Dried blood spots (DBS)</subject><subject>Enzyme-linked immunosorbent assay (ELISA)</subject><subject>Infectious Diseases</subject><subject>International Units/mL</subject><subject>Medicine and Health Sciences</subject><subject>SARS-CoV-2</subject><subject>Serology</subject><subject>Serosurveillance</subject><subject>Vaccination</subject><subject>Virology</subject><issn>1386-6532</issn><issn>1873-5967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ADGLB</sourceid><recordid>eNqdzb9OwzAQBnAPIFH-vMONMERqYppkLW2BSp0axGo59iUxSnzFvvAuvC0JQoiZ6Ybv-313JhapLPMkX8nsQlzG-LZcpit5XyzE59bp1lNkZ-CEoaEwaG8QqAHuEKr1sUo29JpkUKXHhy3s2yfYHfbVGm7dMIye7K-PdzDxb_Y-as-ONbsPBIuMhh35efTP4FypJ48RpswGhxbqnshCPBHHa3He6D7izc-9Etnj7mXznLQdela9qwMazYq0UzqYbnqlxnaOalRlkcuiLOS_0BeqIWMv</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Meyers, Eline</creator><creator>Coen, Anja</creator><creator>De Sutter, An</creator><creator>Padalko, Elizaveta</creator><creator>Callens, Steven</creator><creator>Vandekerckhove, Linos</creator><creator>Witkowski, Wojciech</creator><creator>Heytens, Stefan</creator><creator>Cools, Piet</creator><scope>ADGLB</scope></search><sort><creationdate>2022</creationdate><title>Diagnostic performance of the SARS-CoV-2 S1RBD IgG ELISA (immunodiagnostics) for the quantitative detection of SARS-CoV-2 antibodies on dried blood spots</title><author>Meyers, Eline ; Coen, Anja ; De Sutter, An ; Padalko, Elizaveta ; Callens, Steven ; Vandekerckhove, Linos ; Witkowski, Wojciech ; Heytens, Stefan ; Cools, Piet</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-ghent_librecat_oai_archive_ugent_be_87637873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Dried blood spots (DBS)</topic><topic>Enzyme-linked immunosorbent assay (ELISA)</topic><topic>Infectious Diseases</topic><topic>International Units/mL</topic><topic>Medicine and Health Sciences</topic><topic>SARS-CoV-2</topic><topic>Serology</topic><topic>Serosurveillance</topic><topic>Vaccination</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Meyers, Eline</creatorcontrib><creatorcontrib>Coen, Anja</creatorcontrib><creatorcontrib>De Sutter, An</creatorcontrib><creatorcontrib>Padalko, Elizaveta</creatorcontrib><creatorcontrib>Callens, Steven</creatorcontrib><creatorcontrib>Vandekerckhove, Linos</creatorcontrib><creatorcontrib>Witkowski, Wojciech</creatorcontrib><creatorcontrib>Heytens, Stefan</creatorcontrib><creatorcontrib>Cools, Piet</creatorcontrib><collection>Ghent University Academic Bibliography</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meyers, Eline</au><au>Coen, Anja</au><au>De Sutter, An</au><au>Padalko, Elizaveta</au><au>Callens, Steven</au><au>Vandekerckhove, Linos</au><au>Witkowski, Wojciech</au><au>Heytens, Stefan</au><au>Cools, Piet</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnostic performance of the SARS-CoV-2 S1RBD IgG ELISA (immunodiagnostics) for the quantitative detection of SARS-CoV-2 antibodies on dried blood spots</atitle><date>2022</date><risdate>2022</risdate><issn>1386-6532</issn><issn>1873-5967</issn><abstract>Dried Blood Spots (DBS) are broadly used in SARS-CoV-2 surveillance studies, reporting either the presence or absence of SARS-CoV-2 antibodies. However, quantitative follow-up has become increasingly important to monitor humoral vaccine responses. Therefore, we aimed to evaluate the performance of DBS for the detection of anti-spike SARS-CoV-2 antibody concentrations using a commercially available assay, reporting in a standardised unitage (International Units/mL; IU/mL).
To assess the sensitivity and specificity of the ImmunoDiagnostics ELISA on serum and DBS for SARS-CoV-2 antibody detection, we analysed 72 paired DBS and serum samples. The SARS-CoV-2 51 IgG ELISA kit (EUROIMMUN) on serum was used as the reference method. We performed a statistical assessment to optimise the cutoff value for DBS and serum and assessed the correlation between DBS and serum antibody concentrations.
We found that anti-spike SARS-CoV-2 antibody concentrations detected in DBS are highly correlated to those detected in paired serum (Pearson correlation 0.98; p-value < 0.0001), allowing to assess serum antibody concentration using DBS. The optimal cut-off for antibody detection on DBS was found to be 26 IU/mL, with 98.1% sensitivity and 100% specificity. For serum, the optimal cut-off was 14 IU/mL, with 100% sensitivity and 100% specificity.
Therefore, we conclude that the ImmunoDiagnostics ELISA kit has optimal performance in the detection of SARS-CoV-2 antibodies on both DBS and serum. This makes DBS ideal for large-scale follow-up of humoral SARS-CoV-2 immune responses, as it is an easy but valuable sampling method for quantification of SARS-CoV-2 antibodies, compared to serum.</abstract><oa>free_for_read</oa></addata></record> |
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source | Ghent University Academic Bibliography; Elsevier ScienceDirect Journals |
subjects | Dried blood spots (DBS) Enzyme-linked immunosorbent assay (ELISA) Infectious Diseases International Units/mL Medicine and Health Sciences SARS-CoV-2 Serology Serosurveillance Vaccination Virology |
title | Diagnostic performance of the SARS-CoV-2 S1RBD IgG ELISA (immunodiagnostics) for the quantitative detection of SARS-CoV-2 antibodies on dried blood spots |
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