Correlation of Automated Chemiluminescent Method with Enzyme-Linked Immunosorbent Assay (ELISA) Antibody Titers in Convalescent COVID-19 Plasma Samples: Development of Rapid, Cost-Effective Semi-Quantitative Diagnostic Methods.

COVID-19 ELISA antibody chemiluminescence titers

Journal

Journal of blood medicine
ISSN: 1179-2736
Titre abrégé: J Blood Med
Pays: New Zealand
ID NLM: 101550884

Informations de publication

Date de publication:
2021
Historique:
received: 22 12 2020
accepted: 23 02 2021
entrez: 25 3 2021
pubmed: 26 3 2021
medline: 26 3 2021
Statut: epublish

Résumé

We investigated the utility of an automated chemiluminescent SARS-CoV-2 IgG antibody assay platform in quantifying the amount of binding antibodies present in donated convalescent plasma. A total of 179 convalescent plasma units were analyzed for the presence of SARS-CoV-2 IgG antibodies using the Beckman-Coulter chemiluminescent immunoassay (CLIA) platform. The equipment-derived numerical values (S/Co ratio) were recorded. Aliquots from the same units were subjected to enzyme-linked immunosorbent assay (ELISA) that detects IgG antibodies against the receptor-binding domain (RBD) of the SARS-CoV-2 S1 protein. The relationship between ELISA titers and CLIA S/Co values was analyzed using linear regression and receiver operating characteristics (ROC) curve. Twenty-one samples (11.7%) had S/Co values of less than 1.0 and were deemed negative for antibodies and convalescent plasma had S/Co values between >1.0 and 5.0 (70/179, 39.1%). Fifteen units (8.4%) had negative ELISA titer. The majority of the units (95/179. 53.1%) had titers ≥1:1024. The sensitivities of ELISA to CLIA were comparable (90.5% vs 88.3%, respectively; p=0.18). There was positive linear correlation between CLIA S/Co values and ELISA IgG titer (Rho = 0.75; Spearman's rank = 0.82, p-value = <0.0001). The agreement between the two methods was fair, with a κ index of 0.2741. Using the ROC analysis, we identified a CLIA S/Co cutoff value of 8.2, which gives a sensitivity of 90% and a specificity of 82% in predicting a titer dilution of ≥1:1024. The utility of automated antibody detection systems can be extended from simply a screening method to a semi-quantitative and quantitative functional antibody analysis. CLIA S/Co values can be used to reliably estimate the ELISA antibody titer. Incorporation of chemiluminescent-based methods can provide rapid, cost-effective means of identifying anti-SARS-CoV-2 antibody titers in donated plasma for use in the treatment of COVID-19 infection.

Sections du résumé

BACKGROUND BACKGROUND
We investigated the utility of an automated chemiluminescent SARS-CoV-2 IgG antibody assay platform in quantifying the amount of binding antibodies present in donated convalescent plasma.
METHODS METHODS
A total of 179 convalescent plasma units were analyzed for the presence of SARS-CoV-2 IgG antibodies using the Beckman-Coulter chemiluminescent immunoassay (CLIA) platform. The equipment-derived numerical values (S/Co ratio) were recorded. Aliquots from the same units were subjected to enzyme-linked immunosorbent assay (ELISA) that detects IgG antibodies against the receptor-binding domain (RBD) of the SARS-CoV-2 S1 protein. The relationship between ELISA titers and CLIA S/Co values was analyzed using linear regression and receiver operating characteristics (ROC) curve.
RESULTS RESULTS
Twenty-one samples (11.7%) had S/Co values of less than 1.0 and were deemed negative for antibodies and convalescent plasma had S/Co values between >1.0 and 5.0 (70/179, 39.1%). Fifteen units (8.4%) had negative ELISA titer. The majority of the units (95/179. 53.1%) had titers ≥1:1024. The sensitivities of ELISA to CLIA were comparable (90.5% vs 88.3%, respectively; p=0.18). There was positive linear correlation between CLIA S/Co values and ELISA IgG titer (Rho = 0.75; Spearman's rank = 0.82, p-value = <0.0001). The agreement between the two methods was fair, with a κ index of 0.2741. Using the ROC analysis, we identified a CLIA S/Co cutoff value of 8.2, which gives a sensitivity of 90% and a specificity of 82% in predicting a titer dilution of ≥1:1024.
CONCLUSION CONCLUSIONS
The utility of automated antibody detection systems can be extended from simply a screening method to a semi-quantitative and quantitative functional antibody analysis. CLIA S/Co values can be used to reliably estimate the ELISA antibody titer. Incorporation of chemiluminescent-based methods can provide rapid, cost-effective means of identifying anti-SARS-CoV-2 antibody titers in donated plasma for use in the treatment of COVID-19 infection.

Identifiants

pubmed: 33762863
doi: 10.2147/JBM.S296730
pii: 296730
pmc: PMC7982562
doi:

Types de publication

Journal Article

Langues

eng

Pagination

157-164

Informations de copyright

© 2021 Mendoza et al.

Déclaration de conflit d'intérêts

No conflicting relationship exists for any author.

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Auteurs

Rachelle Mendoza (R)

Department of Pathology, SUNY Downstate Health Sciences University, Brooklyn, NY, USA.

Michael Silver (M)

School of Public Health, SUNY Downstate Health Sciences University, Brooklyn, NY, USA.
Department of Medicine, Maimonides Medical Center, Brooklyn, NY, USA.

Alejandro R Zuretti (AR)

Department of Pathology, SUNY Downstate Health Sciences University, Brooklyn, NY, USA.
Department of Pathology, Maimonides Medical Center, Brooklyn, NY, USA.

Manan Christian (M)

Department of Pathology, Maimonides Medical Center, Brooklyn, NY, USA.

Ballabh Das (B)

Department of Medicine, SUNY Downstate Health Sciences University, Brooklyn, NY, USA.

Allen J Norin (AJ)

Department of Medicine, SUNY Downstate Health Sciences University, Brooklyn, NY, USA.

Patrick Borgen (P)

Department of Surgery, Maimonides Medical Center, Brooklyn, NY, USA.

Jenny Libien (J)

Department of Pathology, SUNY Downstate Health Sciences University, Brooklyn, NY, USA.
Department of Pathology, Maimonides Medical Center, Brooklyn, NY, USA.

Martin H Bluth (MH)

Department of Pathology, Maimonides Medical Center, Brooklyn, NY, USA.

Classifications MeSH