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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Peterhoff, D; Glück, V; Vogel, M; Schuster, P; Schütz, A; Neubert, P; Albert, V; Frisch, S; Kiessling, M; Pervan, P; Werner, M; Ritter, N; Babl, L; Deichner, M; Hanses, F; Lubnow, M; Müller, T; Lunz, D; Hitzenbichler, F; Audebert, F; Hähnel, V; Offner, R; Müller, M; Schmid, S; Burkhardt, R; Glück, T; Koller, M; Niller, HH; Graf, B; Salzberger, B; Wenzel, JJ; Jantsch, J; Gessner, A; Schmidt, B; Wagner, R.
A highly specific and sensitive serological assay detects SARS-CoV-2 antibody levels in COVID-19 patients that correlate with neutralization.
Infection. 2021; 49(1): 75-82. Doi: 10.1007/s15010-020-01503-7 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Kießling Mara Luisa
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Abstract:
OBJECTIVE: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic challenges national health systems and the global economy. Monitoring of infection rates and seroprevalence can guide public health measures to combat the pandemic. This depends on reliable tests on active and former infections. Here, we set out to develop and validate a specific and sensitive enzyme linked immunosorbent assay (ELISA) for detection of anti-SARS-CoV-2 antibody levels. METHODS: In our ELISA, we used SARS-CoV-2 receptor-binding domain (RBD) and a stabilized version of the spike (S) ectodomain as antigens. We assessed sera from patients infected with seasonal coronaviruses, SARS-CoV-2 and controls. We determined and monitored IgM-, IgA- and IgG-antibody responses towards these antigens. In addition, for a panel of 22 sera, virus neutralization and ELISA parameters were measured and correlated. RESULTS: The RBD-based ELISA detected SARS-CoV-2-directed antibodies, did not cross-react with seasonal coronavirus antibodies and correlated with virus neutralization (R2 = 0.89). Seroconversion started at 5 days after symptom onset and led to robust antibody levels at 10 days after symptom onset. We demonstrate high specificity (99.3%; N = 1000) and sensitivity (92% for IgA, 96% for IgG and 98% for IgM; > 10 days after PCR-proven infection; N = 53) in serum. CONCLUSIONS: With the described RBD-based ELISA protocol, we provide a reliable test for seroepidemiological surveys. Due to high specificity and strong correlation with virus neutralization, the RBD ELISA holds great potential to become a preferred tool to assess thresholds of protective immunity after infection and vaccination.
Find related publications in this database (using NLM MeSH Indexing)
Antibodies, Neutralizing - blood
Antibodies, Viral - blood
Antigens, Viral - chemistry, immunology
COVID-19 - blood, diagnosis, immunology, virology
Cross-Sectional Studies - administration & dosage
Enzyme-Linked Immunosorbent Assay - standards
Humans - administration & dosage
Immune Sera - chemistry
Immunoglobulin A - blood
Immunoglobulin G - blood
Immunoglobulin M - blood
Neutralization Tests - standards
Protein Domains - administration & dosage
SARS-CoV-2 - immunology
Sensitivity and Specificity - administration & dosage
Spike Glycoprotein, Coronavirus - chemistry, immunology

Find related publications in this database (Keywords)
SARS-CoV-2
COVID-19
Antibody test
ELISA
Serology
Virus neutralization
Assay validation
Spike protein
S protein
Receptor binding domain
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