Summary & Overview
CPT 86816: HLA Class II Serologic Typing, Single Antigen (DR or DQ)
CPT code 86816 designates a serologic laboratory test that identifies a single human leukocyte antigen (HLA) specificity within HLA Class II, focused on the DR and DQ loci. This code is used for targeted HLA typing in clinical contexts such as transplant matching, immunogenetics, and diagnostic evaluation of immune-mediated conditions. Nationally, accurate reporting of HLA testing codes supports care coordination for transplantation and establishes clinical documentation for payer adjudication.
Key payers covered in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise summary of the clinical context for CPT code 86816, typical sites of service, and the types of information payers commonly consider for laboratory HLA testing claims.
This publication provides benchmarks and policy-relevant context rather than clinical guidance. It outlines typical utilization contexts, common modifiers used with laboratory procedures (listed elsewhere in the document), and highlights areas where payers may request medical necessity documentation. Data not provided in the input, such as associated taxonomies, ICD-10 diagnoses, and payer-specific coverage edits, are noted as unavailable in the relevant sections.
Billing Code Overview
CPT code 86816 describes a serologic test to identify a single human leukocyte antigen (HLA) from HLA Class II cell surface antigens, specifically the DR and DQ loci. The procedure involves laboratory analysis to detect one HLA specificity using serologic methods.
Service type: Laboratory — HLA Class II serologic typing (single antigen, DR or DQ)
Typical site of service: Clinical laboratory or hospital pathology service (inpatient or outpatient lab setting)
Clinical & Coding Specifications
Clinical Context
A 42-year-old patient with end-stage renal disease is being evaluated for kidney transplantation. The transplant center orders HLA Class II typing focused on DR and DQ loci to identify recipient HLA antigens for donor-recipient matching and crossmatch interpretation. A phlebotomy technician obtains a blood sample in an anticoagulated tube and sends it to the immunogenetics laboratory. The laboratory analyst performs a serologic HLA Class II test for one or more DR and/or DQ specificities using standard microlymphocytotoxicity or flow-based serologic methods; results are reported to the transplant team and entered into the laboratory information system. The workflow includes specimen accessioning, cell separation or preparation, performance of the serologic assay, quality control, interpretation by a qualified laboratory professional, and issuance of a final report that feeds into donor selection and anti-HLA antibody assessment.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when only the professional (interpretation) component is billed separately from the technical component. |
TC | Technical component | Use when only the technical component (lab processing and testing) is billed. |