T-Detect Lyme
Enabling accurate detection of early Lyme disease.
T-Detect Lyme
Enabling accurate detection of early Lyme disease.
Suspect your patient has early Lyme disease?
T-DetectTM Lyme reveals a patient’s adaptive immune system response to the bacteria that causes Lyme disease, Borrelia burgdorferi, and helps provide a reliable answer. 1
Standard two-tiered testing (STTT) may have lower sensitivity in detecting early Lyme disease.1-3

T-Detect Lyme can identify early Lyme disease with greater sensitivity than standard two-tiered testing (STTT).1
Sensitivity
In a recent study, T-Detect Lyme showed 3 times greater sensitivity than the standard of care, STTT, in the first four days after symptoms appeared.1
In the clinical validation study, T-Detect Lyme showed 1.5 times greater sensitivity than STTT among patients with early Lyme disease.4
Specificity
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References
- Greissl J, Pesesky M, Dalai SC, et al. Immunosequencing of the T-cell receptor repertoire reveals signatures specific for diagnosis and characterization of early Lyme disease. MedRxIv. 2021. https://doi.org/10.1101/2021.07.30.21261353.
- Marques AR. Revisting the Lyme disease serodiagnostic algorithm: the momentum gathers. J Clin Microbiol. 2018;56(8):e00749-18. doi: 10.1128/JCM.00749-18.
- Nadelman RB, Nowakowski J, Forseter G, et al. The clinical spectrum of early Lyme borreliosis in patients with culture-confirmed erythema migrans. Am J Med. 100;5:502-508. doi: https://doi.org/10.1016/S0002-9343(95)99915-9.
- Data on file. Adaptive Biotechnologies. 2022.
*Based on a population of endemic and non-endemic asymptomatic negative subjects.
T-Detect Lyme is not available in New York.
T-Detect Lyme is for prescription use only. For in vitro diagnostic use only. The CLIA laboratory-developed test (LDT) service has not been cleared or approved by the U.S. Food and Drug Administration (FDA) for this intended use. T-Detect Lyme is not indicated for use in patients under age 18.