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HelpTest Code HTLV Human T-Cell Lymphotropic Virus Types I and II Antibody Screen with Confirmation, Serum
Reporting Name
HTLV-I/-II Ab Screen, SPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Useful For
Qualitative detection of human T-cell lymphotropic virus types I and II (HTLV-I and HTLV-II)-specific antibodies with confirmation and differentiation between HTLV-I and HTLV-II infection
This test should not be used to screen blood, human cells, tissues, or solid-organ donors.
This test is not intended for use on cord blood specimens.
Ordering Guidance
This test is for serum specimens only. For spinal fluid specimens, order HTLVC / Human T-Cell Lymphotropic Virus Types 1 and 2 (HTLV-1/-2) Antibody Screen with Confirmation, Spinal Fluid.
Necessary Information
Date of collection is required.
Specimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Centrifuge blood collection tube per collection tube manufacturer's instructions (eg, centrifuge within 2 hours of collection for BD Vacutainer tubes).
2. Aliquot serum into plastic vial.
Specimen Minimum Volume
0.6 mL
Specimen Type
SerumSpecimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Serum | Frozen (preferred) | 28 days | |
| Refrigerated | 7 days |
Day(s) Performed
Monday, Tuesday, Thursday, Friday
Reference Values
Negative
Testing Algorithm
If the human T-cell lymphotropic virus types I and II (HTLV-I/-II) antibody screen is reactive, then HTLV-I/-II antibody confirmation by line immunoassay will be performed at an additional charge.
Reflex Tests
| Test ID | Reporting Name | Available Separately | Always Performed |
|---|---|---|---|
| HTLVL | HTLV-I/-II Ab Confirmation, S | Yes | No |
Method Name
Enzyme Immunoassay (EIA)
Test Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
86790
86689 (if appropriate)
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| HTLVI | HTLV-I/-II Ab Screen, S | 29901-6 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 9539 | HTLV-I/-II Ab Screen, S | 29901-6 |
Report Available
1 to 4 daysForms
If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.