Anti-Burnet Phage Antibody (IgG) by Immunoassay
This test measures the level of antibodies against the Burnet phage in your blood, which may help identify certain immune responses or infections.
["This test helps assess immune system activity related to specific viral exposures or autoimmune conditions."]
Key facts at a glance
- LOINC
- 44814-2
- Short code
- COX2IGM
- Synonyms
- C burnet Ph2 IgM Titr Ser IF
- Category
- chemistry
- Sample
- serum
- Container
- Serum separator tube (SST, gold-top) or red-top tube (no anticoagulant)
- Units
- N/A
- Ref low
- 0
- Ref high
- 1
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- Immunofluorescence assay (IFA) for detection of IgM antibodies against Coxiella burnetii phase 2 antigen
- CPT
- 86638
- SNOMED
- 31361000119108
- Specimen volume
- 1.0 mL serum (minimum 0.5 mL)
- Stability
- Stable at room temperature (20–25°C) for 8 hours; refrigerated (2–8°C) for 7 days; frozen (-20°C or below) for up to 30 days. Avoid repeated freeze-thaw cycles.
- Hemolysis max
- 100
- Lipemia max
- 200
- Icterus max
- 40
- TAT
- 24–96 hours
- Order
- routine
What Is This Test Measuring?
The Burnet phage is a bacteriophage (a virus that infects bacteria) used in research to study immune responses. This test detects IgG antibodies produced in response to exposure to this phage, which can be part of a broader immune reaction to pathogens or experimental stimuli.
Why Might You Need This Test?
Testing for anti-Burnet phage antibodies is often done in research or specialized clinical settings to evaluate immune responses, particularly in studies involving vaccines, autoimmune conditions, or immune-related diseases. It may also be used in certain diagnostic contexts where phage-based assays are employed.
How Is the Sample Collected?
A blood sample is drawn from a vein, usually in your arm, by a healthcare professional. The blood is then processed to separate the serum or plasma for testing.
What Does the Result Mean?
Results are qualitative (positive or negative) and indicate the presence or absence of antibodies against the Burnet phage. A positive result suggests an immune response has occurred, while a negative result means no detectable antibodies were found.
Reference range
Titer <1:16 (Negative): No detectable IgM antibodies to phase 2 antigen. Titer ≥1:16 (Positive): Indicates recent or acute infection with Coxiella burnetii (Q fever). Titer 1:16–1:256 (Indeterminate/Low positive): Suggest repeat testing in 2–4 weeks. Titer ≥1:200 (Strong positive): Consistent with acute Q fever infection.N/A
No fasting or special preparation required. Patients should inform their healthcare provider of any recent vaccinations, current infections, or immunosuppressive therapy, as these may affect antibody response. Acute and convalescent serum samples (2–4 weeks apart) are recommended for accurate serologic diagnosis.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Short name
Anti-Burnet Phage Antibody (IgG)
Frequently asked questions
What Are Common Causes of Abnormal Results?
How Often Should This Test Be Done?
What Should I Do If My Results Are Abnormal?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 15, 2026. · Read our editorial policy