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GTR Home > > Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), Spike Antibody, Semi-Quantitative, Serum

Overview

Test order codeHelp: COVSQ

Test name

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Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), Spike Antibody, Semi-Quantitative, Serum (SARS-CoV-2 Spike Ab, Semi-Quant, S)

Purpose of the test

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This is a clinical microbial test intended for Help: Screening

Condition

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How to order

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CPT Code 86769. Contact Customer Service (https://www.mayocliniclabs.com/customer-service/contacts.html)
Order URL Help: https://www.mayocliniclabs.com/order-tests/account-setup.html

Specimen source

Serum

Sample requirements

For details on sample collection, see https://www.mayocliniclabs.com/test-catalog/Specimen/614035

Turnaround time

Same day Monday through Saturday

Methodology

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Serology
OAntibody assay
Electrochemiluminescence Immunoassay (ECLIA)
  • cobas Elecsys Anti-SARS-CoV-2 S Antibody (Roche Diagnostics)

Summary of what is tested

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Clinical utility

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Not provided

Clinical validity

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Not provided

Comments about the test interpretation (e.g. clinical implication of test results)

This assay provides qualitative and semi-quantitative results for the presence of antibodies to the receptor binding domain (RBD) on the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike glycoprotein. Both vaccine and active infection can stimulate antibodies against this domain. Negative: No antibodies to SARS-CoV-2 spike glycoprotein detected. Negative results may occur in serum collected too soon following infection or vaccination, in immunosuppressed patients or in patients with mild or asymptomatic infection. This test does not rule out active or recent coronavirus disease 2019 (COVID-19) infection or vaccination. Follow up testing with a molecular test for SARS-CoV-2 is recommended in symptomatic patients. Positive: Antibodies to the SARS-CoV-2 spike glycoprotein detected. These results suggest recent or prior SARS-CoV-2 infection or vaccination. No minimum antibody level or threshold has been established to indicate long-term protective immunity against re-infection. Correlation with epidemiologic risk factors and other clinical and laboratory findings is recommended. Serologic results should not be used to diagnose recent SARS-CoV-2 infection. False-positive results for IgG antibodies may occur due to cross-reactivity from pre-existing antibodies or other possible causes.

Clinical resources

Practice guidelines

  • NICE, 2024
    UK NICE Guideline NG191, COVID-19 rapid guideline: managing COVID-19, 2024

Consumer resources

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.