Test ID FINA NAbFeron (IFNB-1) Neutralizing Antibody Test
Specimen Required
Specimen Type: Serum
Container/Tube: Red or SST
Specimen Volume: 2 mL
Collection Instructions: Draw blood in a plain red-top tube(s), serum gel tube is acceptable. Spin down and send 2 mL of serum refrigerate in a plastic vial.
Note: Sample needs to be collected either before treatment with interferon or more than 24 hours following the most recent dose. Patient should not be on steroid therapy for at least two weeks prior to testing.
Secondary ID
91447Useful For
Detection of antibodies to interferon-B-1
Method Name
Viral cytopathic effect assay
Reporting Name
NAbFeron (IFN-B) AntibodySpecimen Type
SerumSpecimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | |
---|---|---|---|
Serum | Refrigerated (preferred) | 28 days | |
Frozen | 180 days | ||
Ambient | 72 hours |
Reference Values
Final report has been sent to the referring laboratory.
Cautions
The present of neutralizing antibodies to interferon beta, especially in persistently high titers, may be associated with reduction in the clinical effectiveness of interferon beta therapy (1). Although the measurement of Nabs can add to the clinical and imaging information used to assess the efficacy of interferon beta therapy, these results should be interpreted in the context of clinical presentation and medical history (2, 3).
Although rare, false positive or false negative results may occur. All results should be interpreted in the context of clinical findings, relevant history, and other laboratory data.
Day(s) Performed
Monday through Friday
Report Available
14 to 25 daysPerforming Laboratory
Athena DiagnosticsTest Classification
This test was developed and its analytical performance characteristics have been determined by Athena Diagnostics. It has not been cleared or approved by U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes. .CPT Code Information
86382