What is the process for ordering Covid antibody testing for a patient?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: February 2, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

How to Order COVID-19 Antibody Testing

COVID-19 antibody testing should be ordered through your laboratory's standard serology ordering system, specifying SARS-CoV-2 IgG and/or IgM antibody testing, but understand that antibody tests are NOT recommended for diagnosing acute COVID-19 infection—they detect past exposure or immune response after infection or vaccination. 1

When Antibody Testing Is Appropriate

Valid Clinical Indications:

  • Determining past SARS-CoV-2 exposure in patients who were never tested during acute illness but have clinical history suggesting prior COVID-19 2, 3
  • Assessing immune response after vaccination or documented infection for research or epidemiological purposes 4, 3
  • Seroprevalence studies at the population level to evaluate community exposure rates 3
  • Evaluating cellular immunity when combined with T-cell assays (ELISpot) in patients with suspected prior infection but no detectable antibodies 3

When NOT to Order Antibody Testing:

  • Never use antibody tests to diagnose acute COVID-19 in symptomatic patients—antigen or NAAT testing is required instead 1
  • Do not use antibody tests to screen for active infection before procedures or hospital admission 1
  • Avoid using antibody tests to determine immunity status for workplace screening, as the correlation with protective immunity remains unclear 1, 3

Practical Ordering Process

Step 1: Select the Appropriate Test Type

  • ELISA or chemiluminescence immunoassays (CLIA) offer higher sensitivity (96% for IgG) and specificity (98%) compared to rapid lateral flow tests 5
  • Laboratory-based testing is preferred over point-of-care rapid tests for clinical decision-making due to superior performance characteristics 3, 5
  • Specify IgG testing as the primary target, since IgM has lower sensitivity (15-70%) and adds limited clinical value 5

Step 2: Order Through Your Laboratory System

  • Use standard serology order codes such as "SARS-CoV-2 antibody, IgG" or "COVID-19 serology panel" depending on your institution's nomenclature 4
  • Collect serum or plasma samples using standard venipuncture technique—whole blood can be used for point-of-care tests but is less reliable 5
  • Ensure at least 14-21 days have elapsed since symptom onset or exposure, as antibody sensitivity is low in the first week and peaks after 2-3 weeks 2, 6

Step 3: Interpret Results with Critical Caveats

Positive Antibody Result:

  • Indicates past SARS-CoV-2 exposure through infection or vaccination, not necessarily current infection 2, 3
  • Does not confirm protective immunity or predict protection against reinfection 3
  • May reflect cross-reactivity with other coronaviruses, particularly in patients with autoimmune disease, though specificity is generally high (98%) 6, 5

Negative Antibody Result:

  • Does not rule out past infection, as some patients never develop detectable antibodies or antibody levels wane over time 6, 3
  • Consider T-cell testing (ELISpot) if clinical suspicion for prior infection remains high despite negative serology 3
  • May occur in immunocompromised patients who mount inadequate humoral responses 6

Critical Pitfalls to Avoid

  • Do not order antibody tests for acute diagnosis—this is the most common misuse; symptomatic patients require antigen or NAAT testing within 5 days of symptom onset 1, 7
  • Do not assume positive antibodies equal immunity—the correlation between antibody levels and protection against infection or severe disease is not established 3
  • Do not test too early—antibody tests have poor sensitivity (<50%) in the first week after exposure and should be delayed until at least 14 days post-symptom onset 2, 6
  • Do not use rapid point-of-care tests for clinical decisions when laboratory-based ELISA/CLIA is available, as rapid tests have significantly lower sensitivity (85-87% vs. 96%) 5
  • Do not interpret negative antibody results as definitive absence of prior infection—cellular immunity may be present without detectable antibodies 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Antibody tests for COVID-19.

Proceedings (Baylor University. Medical Center), 2020

Research

How to interpret and use COVID-19 serology and immunology tests.

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 2021

Guideline

Optimal Timing for Home Flu and COVID Combo Testing After Symptom Onset

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.