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Human T-Cell Lymphotropic Virus 1 and 2 Antibodies (HTLV-1/HTLV-2), Qualitative

Order Code
1226008
CPT
86790
Test Details
Synonyms

HTLV‑1/2 Antibody Test HTLV‑I/II Ab, Qualitative HTLV‑1 and HTLV‑2 Screening Test

TAT

Up to 72 hours

Methodology

Electrochemiluminescence Immunoassay (ECLIA)

Reference Interval

Non-reactive

Performing Location

Accredited NRL Laboratory

Testing Frequency

3 times per week

Test Overview

Testing for antibodies to Human T‑lymphotropic virus type 1 (HTLV-1) and Human T‑lymphotropic virus type 2 (HTLV-2) is used to detect current or past infection. It supports screening of blood and organ donors, diagnosis of associated conditions such as Adult T‑cell leukemia/lymphoma and HTLV‑1 associated myelopathy/tropical spastic paraparesis and helps guide counseling to reduce transmission through blood exposure or breastfeeding.

Specimen Type

Serum or Plasma

Volume

Minimum 0.5 mL

Specimen Container

Serum (SST; Gold Top or plain serum; Red Top) - Preferred Lithium Heparin Plasma (Green Top) - acceptable

Patient Preparation

No special preparation is required for this test. You may eat, drink, and take your medications as normal, unless instructed otherwise by your healthcare provider.

Collection

This test does not require any special collection or pre-analytical handling.
Follow routine specimen collection protocols.

Specimen Stability
Temperature Period
Refrigerated 14 days
Frozen 3 months
Order Code
1226008
CPT
86790
Test Details
Synonyms

HTLV‑1/2 Antibody Test HTLV‑I/II Ab, Qualitative HTLV‑1 and HTLV‑2 Screening Test

TAT

Up to 72 hours

Methodology

Electrochemiluminescence Immunoassay (ECLIA)

Reference Interval

Non-reactive

Performing Location

Accredited NRL Laboratory

Testing Frequency

3 times per week

Test Overview

Testing for antibodies to Human T‑lymphotropic virus type 1 (HTLV-1) and Human T‑lymphotropic virus type 2 (HTLV-2) is used to detect current or past infection. It supports screening of blood and organ donors, diagnosis of associated conditions such as Adult T‑cell leukemia/lymphoma and HTLV‑1 associated myelopathy/tropical spastic paraparesis and helps guide counseling to reduce transmission through blood exposure or breastfeeding.

Specimen Type

Serum or Plasma

Volume

Minimum 0.5 mL

Specimen Container

Serum (SST; Gold Top or plain serum; Red Top) - Preferred Lithium Heparin Plasma (Green Top) - acceptable

Patient Preparation

No special preparation is required for this test. You may eat, drink, and take your medications as normal, unless instructed otherwise by your healthcare provider.

Collection

This test does not require any special collection or pre-analytical handling.
Follow routine specimen collection protocols.

Specimen Stability
Temperature Period
Refrigerated 14 days
Frozen 3 months