Introducing a new test for the quantitative determination of antibodies against the SARS-CoV-2 spike protein - Roche Elecsys® Anti-SARS-CoV-2 S.
This blood test enables the determination of both the presence and level of antibodies to the SARS-CoV-2 spike protein, which is the target of many COVID-19 vaccines,. It can can signal whether a person has already been infected and has potentially developed immunity to the virus., and plays an important part in characterising a vaccine-induced immune response.
If an individual has been infected with SARS-CoV-2 they may have detectable antibodies to both the Nucleocapsid (N) and the Receptor Binding Domain (RBD) Spike antigens. Baseline antibody tests for both N and RBD antigens are therefore helpful to identify patients who have been previously infected with SARS-CoV-2.
If an individual has been vaccinated against SARS-CoV-2, with no history of natural infection, the antibodies they develop are to the RBD Spike antigen. As this test targets antibodies against the spike protein, the levels of these antibodies could play a role in establishing vaccine efficacy and vaccine-induced immune response.
Structure of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2).
Source: https://diagnostics.roche.com/global/en/products/params/elecsys-anti-sars-cov-2.html
Roche Elecsys |
Roche Elecsys |
Abbott |
|
---|---|---|---|
Platform |
Roche e801 |
Roche e801 |
Abbott Architect |
Assay type |
Electrochemiluminescence immunoassay (ECLIA) |
Electrochemiluminescence immunoassay (ECLIA) |
Electrochemiluminescence immunoassay (ECLIA) |
Reporting format |
QUANTITATIVE |
Qualitative |
Qualitative |
Reporting ranges |
Positive with value reported in U/ml / Negative |
Positive / Negative |
Positive / Negative |
Antigen used |
Receptor binding domain (RBD) of Spike antigen |
Nucleocapsid |
Nucleocapsid |
Analyte target |
SARS-CoV-2 Antibodies |
SARS-CoV-2 Antibodies (IgG/IgM) Total Antibody |
SARS-CoV-2 Antibodies (IgG) |
Sample type verified |
Serum – Venous or Capillary self-collection |
Serum – Venous or Capillary self-collection |
Serum – Venous |
Sensitivity |
99.98% |
97.4% |
99.1% |
Specificity |
98.8% in samples taken 14 days or later after positive PCR |
100% |
100% |
Seasonal Corona |
24/24 Negative |
26/26 Negative |
26/26 Negative |
Example reports
Structure of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2).
Source: https://diagnostics.roche.com/global/en/products/params/elecsys-anti-sars-cov-2.html
Sample type |
|
---|---|
Roche Elecys Anti-SARS-CoV-2 S |
Serum: Venous/Capillary self-collection |
Roche Elecys Anti-SARS-CoV-2 IgG/IgM Total Antibody |
Serum: Venous/Capillary self-collection |
Abbott Anti-SARS-CoV-2 IgG |
Serum: Venous |
Reporting format |
|
---|---|
Roche Elecys Anti-SARS-CoV-2 S |
QUANTITATIVE |
Roche Elecys Anti-SARS-CoV-2 IgG/IgM Total Antibody |
Qualitative |
Abbott Anti-SARS-CoV-2 IgG |
Qualitative |
Antigen used |
|
---|---|
Roche Elecys Anti-SARS-CoV-2 S |
RBC of SPIKE Antigen |
Roche Elecys Anti-SARS-CoV-2 IgG/IgM Total Antibody |
Nucleocapsid |
Abbott Anti-SARS-CoV-2 IgG |
Nucleocapsid |
Sample stability |
|
---|---|
Roche Elecys Anti-SARS-CoV-2 S |
7 days |
Roche Elecys Anti-SARS-CoV-2 IgG/IgM Total Antibody |
7 days |
Abbott Anti-SARS-CoV-2 IgG |
7 days |
Please note:
- Antibody tests cannot diagnose acute infection.
- Not everyone will develop an antibody response to COVID infection or vaccine.
- Timing of seroconversion following vaccine ≥ 14 days.
- Results from different manufacturers of commercial assays should not be compared