BK Virus IgG Antibody (ELISA)
Determining the level of anti-BKV IgG antibodies in both kidney donor and recipient has been reported to be a possible factor in predicting the risk of BK nephropathy, an important cause of allograft dysfunction. Moreover, recent scientific data has shown that BK nephropathy in pediatric kidney recipients is associated with the recipients’ BKV seronegativity pre-transplant, indicating a potential need for pre-transplant BKV serological testing.
ProcedureIndirect Enzyme-Linked Immunosorbent Assay (ELISA)
This test has not been cleared or approved for diagnostic use by the U.S. Food and Drug Administration.
SpecificityThe ELISA detects human IgG antibodies to the BKV VP1 protein.
1-7 business days from receipt of specimen
Specimen Type | Test Code | CPT Code | NY Approved | Volume | Assay Range | Special Instructions |
---|---|---|---|---|---|---|
plasma | 2301 | 86790 | No | 2 mL (min. 0.1 mL) |
Antibody titers from <40 to >163840. Test results are reported as an antibody titer, which is the inverse of the specimen dilution that produces signal greater than the assay background level (e.g. 1:2560 specimen dilution is reported as 2560). |
|
serum | 2310 | 86790 | No | 2 mL (min. 0.1 mL) |
Antibody titers from <40 to >163840. Test results are reported as an antibody titer, which is the inverse of the specimen dilution that produces signal greater than the assay background level (e.g. 1:2560 specimen dilution is reported as 2560). |
|
Antibody titers from <40 to >163840. Test results are reported as an antibody titer, which is the inverse of the specimen dilution that produces signal greater than the assay background level (e.g. 1:2560 specimen dilution is reported as 2560).
ShippingShip Monday through Friday. Friday shipments must be labeled for Saturday delivery. All specimens must be labeled with patient's name and collection date. A Eurofins Viracor test requisition form must accompany each specimen. Multiple tests can be run on one specimen. Ship specimens FedEx Priority Overnight® to: Eurofins Viracor, 18000 W 99th St. Ste, #10, Lenexa, KS 66219
Causes for RejectionSpecimens beyond their acceptable length of time from collection as indicated in the specimen handling or specimen types other than those listed.
Specimens are approved for testing in New York only when indicated in the Specimen Information field above.
The CPT codes provided are based on Eurofins Viracor's interpretation of the American Medical Association's Current Procedural Terminology (CPT) codes and are provided for informational purposes only. CPT coding is the sole responsibility of the billing party. Questions regarding coding should be addressed to your local Medicare carrier. Eurofins Viracor assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.
The BKV IgG Antibody test is performed pursuant to a licensed agreement with the National Institutes of Health.