Summary & Overview
CPT 86480: TB Interferon-Gamma Cell-Mediated Immunity Assay
CPT code 86480 represents a laboratory immunologic assay that measures the gamma interferon antigen response to tuberculosis antigens, evaluating cell-mediated immunity. This test is used clinically to detect immune sensitization to TB and can inform diagnostic pathways for latent or active infection. Nationally, the code matters because TB screening and diagnosis rely on scalable, standardized laboratory methods that affect public health surveillance and clinical management.
Key payers covered in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find an overview of clinical context for the assay, commonly associated sites of service, and the scope of reimbursement considerations across major payers. The publication summarizes available benchmarks, coding guidance, and pertinent policy updates affecting coverage and billing for interferon-gamma release assays.
The report provides practical reference material for billing staff, laboratory managers, and compliance teams by outlining the clinical purpose of the test, typical practice settings, and the payer landscape. Data not available in the input is noted where applicable.
Billing Code Overview
CPT code 86480 describes a laboratory test performed by a lab analyst to evaluate cell-mediated immunity by measuring the gamma interferon antigen response to tuberculosis (TB) antigens. The service assesses immune system activation specific to TB and aids in identifying prior sensitization or infection.
Service Type: Laboratory diagnostic test, immunologic assay
Typical Site of Service: Clinical laboratory or hospital laboratory
Data not available in the input.
Clinical & Coding Specifications
Clinical Context
A 35-year-old outpatient presents to a primary care clinic for tuberculosis exposure evaluation after close contact with a coworker newly diagnosed with active pulmonary TB. The clinician documents prior Bacillus Calmette–Guérin (BCG) vaccination in childhood and requests an interferon-gamma release assay (IGRA) to assess cell-mediated immune response to Mycobacterium tuberculosis antigens. A phlebotomy technician collects a blood specimen using the manufacturer-recommended tube and timely courier transport is arranged to the reference laboratory. At the laboratory, a trained technologist incubates the specimen with specific TB antigens, measures interferon-gamma release, and reports qualitative/quantitative results. Results are routed back to the ordering clinician for interpretation in the context of risk factors and chest radiography if indicated. Typical site of service is an outpatient clinic, public health clinic, or reference laboratory; specimen collection occurs in clinic and assay performance occurs in the clinical laboratory. Typical patient scenarios include screening of healthcare workers, contacts of active TB cases, asylum seekers or immigrants, and pre-employment or pre-procedural TB screening.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when billing only the professional interpretation component if separated from the technical lab component (rare for automated IGRA but applicable when separate professional interpretation is billed). |
59 | Distinct procedural service | Use when the IGRA is performed on a different encounter or distinct from other lab services on the same day that might be bundled. |
91 | Repeat clinical diagnostic lab test | Use when the same IGRA is repeated on the same day for confirmation or device failure. |
90 | Reference (outside) laboratory | Use when the performing laboratory is an outside or reference lab billing for the service. |
TC | Technical component | Use when billing only the technical component (laboratory processing) and the professional component is billed separately. |
91 | Repeat clinical diagnostic lab test | Use when repeating the assay for verification after an indeterminate result. |
QW | CLIA waived test | Not typically applicable to IGRA (most IGRAs are moderate complexity); include only if the specific kit is CLIA-waived. |
QK | CLIA provider performed microscopy (PPM) | Rare for this assay; include only if performed under specific PPM circumstances per payer rules. |
90 | Reference (outside) laboratory | Use when specimen is sent to an outside reference lab and that lab bills for the service. |
91 | Repeat clinical diagnostic lab test | Use for repeats due to unacceptable specimen or indeterminate result. |
| Taxonomy Code | Specialty | Notes |
|---|---|---|
| 207Q00000X | Infectious Disease | Specialists who may order and interpret TB testing in complex cases. |
| 208000000X | Pathology & Laboratory Medicine | Pathologists and laboratory directors overseeing assay validation and result reporting. |
| 2085R0200X | Clinical Laboratory | Clinical laboratory scientists and technicians who perform the IGRA. |
| 208D00000X | Family Medicine | Primary care clinicians who commonly order TB screening tests. |
| 207L00000X | Pulmonary Disease | Pulmonologists involved in evaluation of suspected active TB or latent infection. |
Related Diagnoses
| ICD-10 Code | Description | Clinical Relevance |
|---|---|---|
Z20.0 | Contact with and (suspected) exposure to tuberculosis | Direct indication for TB screening with an IGRA after known exposure. |
Z11.1 | Encounter for screening for respiratory tuberculosis | Routine screening indication for asymptomatic patients at risk; IGRA commonly used. |
Z11.59 | Encounter for screening for other bacterial diseases | Used when TB screening is part of broader infectious disease screening panels. |
R76.11 | Nonspecific reaction to tuberculin skin test | May prompt use of IGRA to clarify immune response when TST is nonspecific. |
R76.12 | Positive tuberculin skin test reaction | Positive TST may be followed by IGRA for confirmation in some clinical contexts. |
Related CPT Codes
| CPT Code | Description | Relationship to This Procedure |
|---|---|---|
86580 | Skin test; tuberculosis, intradermal (e.g., Mantoux) | Alternative initial screening test for TB; may be used in clinic before or instead of an IGRA. |
87631 | Infectious agent detection by nucleic acid (e.g., M. tuberculosis complex), amplified probe technique, multiple targets | Molecular test used when active TB is suspected; performed on respiratory specimens following a positive screening or clinical concern. |
87481 | Infectious agent antigen detection by immunoassay, multiple-step technique; influenza | Example antigen assay workflow; included as a parallel lab testing code type — not specific to TB but shows typical lab testing sequencing. |
99213 | Office or other outpatient visit for the evaluation and management of an established patient | Common visit code for the clinician encounter during which TB exposure assessment and test ordering occur. |
87070 | Culture, bacterial; any other source, aerobic, with isolation and presumptive identification of isolates | Used when specimen culture is indicated for suspected active TB from nonrespiratory sources; part of the diagnostic cascade for active infection. |