Hepatitis Be Antigen
Code:17013|CPT:87350|LOINC:13954-3
| Includes | Hep Be Ag |
|---|
Analysis details
Methodology
- Immunochemiluminometric assay (ICMA)
- Chemiluminescent immunoassay (CLIA)
Expected Turnaround Time
1 day
Special Instructions
- Review use of high‑dose biotin (vitamin B7/vitamin H); discontinue biotin for at least 72 hours before the blood draw
- Do not smoke during the 30 minutes preceding specimen collection
How to use
The Hepatitis B e antigen (HBeAg, HBV e antigen) assay is used with other serologic markers and HBV DNA testing to assess replicative activity and infectiousness in persons with hepatitis B virus infection. In chronic disease, it supports staging and guides decisions on when to initiate therapy, how to monitor during treatment, and how to document response, including HBeAg loss and seroconversion. Detection or clearance of HBeAg also contributes to infection‑control planning and transmission risk counseling. This assay is not intended for the diagnosis of acute hepatitis B infection.
Limitations
Hepatitis B virus (HBV) is a DNA virus that causes both acute and chronic hepatitis worldwide and is associated with substantial morbidity. Transmission occurs through blood and body fluids, including percutaneous exposure, sexual contact, and perinatal spread. Populations at increased risk include healthcare personnel with blood exposure, hemodialysis patients, people who inject drugs, individuals with multiple sexual partners, and infants born to HBV‑infected mothers. HBV expresses several antigens relevant to laboratory testing: HBsAg (surface), HBcAg (core), and HBeAg, a secreted product of the precore/core region. In acute infection, HBeAg appears at about the same time as, or shortly after, HBsAg and usually clears earlier. Its presence signifies active viral replication and high infectivity; HBeAg‑positive serum is several‑fold more infectious than HBsAg‑positive/HBeAg‑negative serum. Persistence of HBeAg beyond approximately 8–10 weeks suggests evolution toward chronic infection, whereas loss of HBeAg with the emergence of anti‑HBe generally indicates reduced replicative activity and therapeutic response. In chronic hepatitis B, reappearance of HBeAg can indicate viral reactivation, frequently in the context of immunosuppression. Mutations in the precore or basal core promoter region may prevent HBeAg production, leading to HBeAg‑negative chronic hepatitis B with ongoing infectivity and replication that are demonstrable by HBV DNA testing. Interpretation of HBeAg should be integrated with HBsAg, anti‑HBe, anti‑HBc (IgM and total), and HBV DNA results. This assay is not intended for diagnosis of acute hepatitis B infection.
| Unit | qualitative | ||||
|---|---|---|---|---|---|
| Reference interval |
| ||||
| Indications | Assessment of patients with a positive hepatitis B surface antigen (HBsAg) result, Longitudinal monitoring of hepatitis B virus infection activity, Baseline, on‑treatment, and post‑treatment evaluation during antiviral therapy for HBV infection |
Specimen Requirements
| Specimen | Serum |
|---|---|
| Container | Gold/Tiger Top (SST, Gel Separator) |
| Volume | 1.5 mL (min 0.5 mL) |
| Storage Instructions | Room temperature, Refrigerated, Frozen |
References
Abara WE, Qaseem A, Schillie S, et al. Hepatitis B vaccination, screening, and linkage to care: Best practice advice from the American College of Physicians and the Centers for Disease Control and Prevention. Ann Intern Med. 2017;167(11):794-804. PubMed 29159414.
Schillie S, Vellozzi C, Reingold A, et al. Prevention of hepatitis B virus infection in the United States: Recommendations of the Advisory Committee on Immunization Practices. MMWR Recomm Rep. 2018;67(1):1-31. PubMed 29939980.
Terrault NA, Lok ASF, McMahon BJ, et al. Update on prevention, diagnosis, and treatment of chronic hepatitis B: AASLD 2018 hepatitis B guidance. Hepatology. 2018;67(4):1560-1599. PubMed 29405329.
Workowski KA, Bolan GA; Centers for Disease Control and Prevention. Sexually transmitted diseases treatment guidelines. MMWR Recomm Rep. 2015;64(RR-03):1-137. PubMed 26042815.
Vozianova ZI. Infectious and Parasitic Diseases. Vol 1. Kyiv: Zdorov'ya; 2000:601-654.
Harrison's Principles of Internal Medicine. 16th ed. New York: McGraw-Hill; 2005:1822-1855.