- ABL Kinase Domain Mutation in CML, Cell-based
- ABO Group and Rh Type
- Acid-Fast Bacillus (AFB) Identification, Sequencing and Stain, Paraffin Block
- ADAMTS13 Activity with Reflex to ADAMTS13 Inhibitor
- Alcohol Metabolites, Quantitative, Urine
- Alpha-Globin Common Mutation Analysis
- Alpha-Globin Gene Deletion or Duplication
- Alpha-Globin Gene Sequencing
- Anti-Müllerian Hormone AssessR™
- Anti-PF4 and Serotonin Release Assay (SRA) for Diagnosing Heparin-induced Thrombocytopenia/Thrombosis (HIT/HITT)
- Antiphospholipid Antibodies
- ASCVD Risk Panel with Score
- Autoimmune Epilepsy Evaluation
- BCR-ABL1 Gene Rearrangement, Quantitative PCR
- B-cell and T-cell Clonality Assays by PCR
- B-Type Natriuretic Peptide (BNP)
- Beta-Globin Complete
- Beta-Lactamase Detection, Comprehensive Gram-negative Bacteria Panel
- BRCAvantage Plus™ Test Menu
- BRCAvantage™, Ashkenazi Jewish Screen
- BRCAvantage™, Comprehensive
- BRCAvantage™, Rearrangement
- BRCAvantage™, Single Site
- Chlamydia trachomatis and Neisseria gonorrhoeae RNA, TMA
- Clostridium difficile Toxin/Glutamate Dehydrogenase (GDH) with Reflex to PCR
- C1 Inhibitor, Protein and Functional Tests
- Calreticulin (CALR) Mutation Analysis
- Carbapenem Resistant Enterobacteriaceae Culture Screen
- Cardio IQ Lipoprotein Fractionation, Ion Mobility
- Cervical Cancer, TERC, FISH
- CFvantage™ Cystic Fibrosis Expanded Screen
- Chlamydia trachomatis, TMA
- Chromosomal Microarray, POC, ClariSure®, Oligo-SNP
- Chromosomal Microarray, Postnatal, ClariSure® Oligo-SNP
- Chromosome Analysis and AFP with Reflex to AChE, Fetal Hgb, Amniotic Fluid
- Chromosome Analysis, Amniotic Fluid
- Chromosome Analysis, Blood
- Chromosome Analysis, Blood with Reflex to Postnatal, ClariSure® Oligo-SNP Array
- Chromosome Analysis, Chorionic Villus Sample
- Chromosome Analysis, High Resolution
- Chromosome Analysis, High Resolution with Reflex to Postnatal, ClariSure® Oligo-SNP Array
- Chromosome Analysis, Mosaicism
- Chromosome Analysis, Neonatal Blood
- Chromosome Analysis, Sister Chromatid Exchange
- Chromosome Analysis, Tissue
- Chromosome DEB Assay for Fanconi anemia
- Chronic Lymphocytic Leukemia (CLL) - Diagnostic and Prognostic Testing
- Culture, Fungus
- Culture, Urine, Routine
- Cystic Fibrosis Screen
- Cytomegalovirus (CMV) and Epstein Barr Virus (EBV) PCR
- D-Dimer, Quantitative
- Dementia, Secondary Causes
- Diabetes Risk Panel with Score and Cardio IQ® Diabetes Risk Panel with Score
- Drug Testing, General Toxicology (Blood, Urine, or Serum)
- Factor V (Leiden) Mutation Analysis
- Familial Mediterranean Fever Mutation Analysis
- First Trimester Screen, hCG
- First Trimester Screen, Hyperglycosylated hCG (h-hCG)
- FISH, MET Amplification
- FISH, Angelman
- FISH, Myeloma, 17p-, rea 14q32 with Reflexes
- FISH, Prader-Willi
- FISH, Prenatal Screen
- No FAQs found
- HCV Genotyping
- Heparin, Anti-Xa
- Hepatitis B Surface Antibody, Quantitative
- Hepatitis C Viral RNA NS3 Genotype
- Hepatitis C, RNA, Quantitative, PCR
- Hereditary Hemochromatosis DNA Mutation Analysis
- Herpes Simplex Virus (HSV) Type-Specific IgG Antibodies (HerpeSelect®)
- Herpes Simplex Virus Type 2 (HSV-2) IgG Inhibition, ELISA
- HIV Infection: Laboratory Testing for Diagnosis
- HIV-1 Coreceptor Tropism with Reflex to Ultradeep Sequencing
- HIV-1 Coreceptor Tropism, Proviral DNA
- HIV-1 Integrase Genotype
- HPV mRNA E6/E7
- Influenza A and B Antigen, Immunoassay
- Influenza Type A and B Antibodies
- Integrated Screen, Part 1
- Integrated Screen, Part 2
- Intrinsic Factor Blocking Antibody
- No FAQs found
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- Maternal Serum AFP
- Melanoma, BRAF V600E and V600K Mutation Analysis, THxID®
- Metanephrines, Fractionated, Free, LC/MS/MS, Plasma
- Methylenetetrahydrofolate Reductase (MTHFR), DNA Mutation Analysis
- Microalbumin (Urinary Albumin Excretion)
- Myelodysplastic Syndrome (MDS) Mutations, Sequencing
- Myeloproliferative Neoplasm Mutations (without BCR-ABL, JAK2, and MPL)
- Pain Management and CYP2D6/CYP2C19
- Partial Thromboplastin Time, Activated (aPTT)
- Penta Screen
- PIK3CA Mutation Analysis
- PNH with FLAER (High Sensitivity)
- Prothrombin Time with INR
- PTH, Intact and Calcium
- Saccharomyces cerevisiae Antibodies (ASCA) (IgG, IgA)
- Sequential Integrated Screen, Part 1
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- Serum Integrated Screen, Part 1
- Serum Integrated Screen, Part 2
- Serum Pregnancy Tests
- Sickle Cell Screen
- Stepwise, Part 1
- Stepwise, Part 2
- SureSwab® Trichomonas vaginalis RNA, Qualitative TMA
- No FAQs found
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QuantiFERON®-TB Gold, (Draw Site Incubated)
Test code(s) 16603
Question 1. What is the QuantiFERON®-TB Gold, (Draw Site Incubated)?
An alternative to the tuberculosis skin test (TST).
The QuantiFERON-TB Gold, (Draw Site Incubated) is a blood test for use as an aid in diagnosing Mycobacterium tuberculosis infection, both latent tuberculosis infection and active tuberculosis disease. This test is considered an interferon gamma release assay (IGRA).
Centers for Disease Control and Prevention (CDC) states: “The greater specificity (as compared to the TST) of the Quantiferon test and the requirement for only one office visit are compelling advantages.”
CDC Specific Recommendations (June 25, 2010 / 59(RR05);1-
- “Interferon Gamma Release Assays (IGRAs) may be used in place of (but not in addition to) a TST in all situations in which the CDC recommends TST as an aid in diagnosing adult M. tuberculosis infections.”
- “IGRA is preferred for testing persons who have received Bacille Calmette-Guérin (BCG) as a vaccine or cancer therapy.”
- “An IGRA may be used in place of TST (without preference) to test recent contacts of persons with infectious tuberculosis with special considerations for follow-up testing. In contact investigations, negative results obtained prior to 8 weeks typically should be confirmed by repeat testing 8-10 weeks after the end of exposure.”
Question 2. How does QuantiFERON-TB Gold, (Draw Site Incubated)?
The QuantiFERON-TB Gold, (Draw Site Incubated) is an indirect test for M tuberculosis infection that is based on measurement of a cell-mediated immune response. A cocktail of 3 mycobacterial proteins (ESAT-6, CFP-10, and TB 7.7) stimulate the patient’s T-cells in vitro to release interferon-gamma, which is then measured using enzyme linked immunoabsorbent assay (ELISA) technology. The test detects infections produced by the M. tuberculosis complex including M tuberculosis, M bovis, and M africanum. Bacilli Calmette-Guérin strains and the majority of other non-tuberculosis mycobacteria do not harbor ESAT-6, CFP-10, and TB 7.7 proteins; thus, patients either vaccinated with bacilli Calmette-Guérin or infected with most environmental mycobateria should test negative. Results should always be interpreted in conjunction with other clinical and laboratory findings.
Question 3. What are the advantages of QuantiFERON-TB Gold, (Draw Site Incubated) over tuberculin skin test (TST)?
- Improved specificity
- Results are not subject to reader bias
- Results are not affected by the booster phenomenon (i.e., increased sensitivity on subsequent test, leading to false-positive results)
- Accuracy is not affected by prior BCG vaccination
- Requires only 1 patient visit (2-4 required for TST)
- Cost savings from reduced staff time and avoidance of unnecessary follow-up testing and treatment
Question 4. How do you interpret the QuantiFERON-TB Gold, (Draw Site Incubated) test result?
An example of a QuantiFERON report is shown below:
Nil or Negative Control Tube (grey cap)
The Nil value comes from the negative control tube that contains no additives; it is used to determine if the patient has a preexisting immune response (i.e., heterophile antibody effects, non-specific gamma interferon production, etc.) which could cause a false-positive reading on the test.
In order for a test to be valid, the Nil tube must have a value of ≤8.0 IU/mL. In the example cited above, the Nil value (0.07 IU/mL) is well within the recommended range of ≤8.0 IU/mL.
Mitogen or Positive Control Tube (purple cap)
The mitogen control tube contains a mitogen (phytohaemogglutin-P), which is a non-specific stimulator of T-cells. It is used to assure the patient has a healthy immune status and also serves as a control for correct blood handling and incubation. It is used to detect false-negative readings.
In order for a test to be valid, the mitogen tube must have a gamma interferon value ≥0.5 IU/mL higher than the value of the Nil tube. This indicates that the mitogen control, as the positive control, is functioning properly.
In the example cited above, the mitogen tube value minus the Nil tube value is well above the minimum breakpoint of ≥0.5 IU/mL.
TB Antigen (red cap)
The inside of this tube is coated with the M tuberculosis specific antigens described above.
For a test to be considered positive, the TB antigen tube value minus the Nil tube value must be ≥0.35 IU/mL (FDA cleared breakpoint). Low positive values (0.35–1.0 IU/mL) may not repeat as positive in some patient populations (see below table); some authorities recommend that the patient be retested to confirm low positive tests.
In the example cited above, the TB antigen tube value minus the Nil tube value is well above the positive breakpoint of 0.35 IU/mL. A positive/detected result suggests that the M. tuberculosis infection is likely. It does not determine if the infection is recent or old, or if the disease is currently active or latent.
Conversions and Reversions – Quantiferon*
Among individuals with quantitative values just above or just below the cut-off threshold, reversions or conversions were common. Retesting was performed within 3 weeks of the original test. Confirming a positive Quantiferon test is prudent before starting therapy.
*Per Susan Dorman, M.D. The John Hopkins University School of Medicine.
Calculation of Detected, Not Detected, or Indeterminate
The amount of gamma interferon produced by each tube (Nil, mitogen, TB antigen) is measured using a standard ELISA format. QuantiFERON-TB Gold, (Draw Site Incubated) results are based on the amount of INF-γ that is released in response to the antigens. The result “Not Detected” or “Detected” is calculated from these values using an FDA approved algorithm run on QuantiFERON software. Indeterminate results are generated when either of the control tubes does not produce their intended values.
Question 5. What causes an indeterminate response?
The 2 main causes of indeterminate results are:
- Lack of incubating the samples properly (such as not incubating the sample at all or over incubating)
- Insufficient mixing of blood collection tubes
Other less common causes are outlined below:
- Presence of heterophile antibodies in the patient sample
- Intrinsic IFN-γ secretion
- Recent patient illness
- Recent vaccinations
- Lymphocytes responding indiscriminately (recent patient bouts with poison ivy, rheumatoid arthritis, etc.)
- Lack of response to phytohaemagglutinin(occurs in less than 1 in 1,000 patients)
- Storage of filled blood collection tubes outside the recommended temperature range (22°C ± 5°C) prior to 37°C ± 1°C incubation
- Compromised mitogen transport tubes
- Compromised immune status of the individual being tested
- Insufficient lymphocytes
- Inability of the patient’s lymphocytes to generate IFN-γ
If an indeterminate result is obtained, the physician may choose to redraw a specimen or perform other procedures as appropriate.
Question 6. Can Quantiferon testing be used to monitor TB therapy?
No. Quantiferon testing cannot be used to monitor TB theapy.5
Question 7. Does prior TB skin testing affect a Quantiferon result?
Yes. IGRAs such as Quantiferon should be performed within 3 days after placing a skin test to avoid the boosting phenomenon.1
- Daley CL, Reves RR, et al. A summary of meeting proceedings on addressing variability around the cut point in erial nterferon-gamma release assay testing. ICHE 2013;34:625-630.
- Diel R, Loddenkemper R, Meywald-Walter K, et al. Comparative performance of tuberculin skin test, QuantiFERON-TB-Gold In Tube Assay, and T-Spot.TB Test in Contact Investigations for Tuberculosis. Chest. 2009;135:1010-1018.
- Diel RR, Loddenkemper R, Nienhaus A. Evidence-based comparison of commercial interferon-gamma release assays for detecting active TB: a metaanalysis. Chest. 2010;149:177-184.
- Horsburgh CR, Rubin EJ. Latent tuberculosis infection in the United States. N Engl J Med. 2011;364:1441-1448.
- Pollock, NR, Kashino SS, et al. Evaluation of the effect of treatment of latent tuberculosis infection on Quantiferon-TB Gold assay results. Infect Control Hosp Epidemiol. 2009;30:1123-1126.