Summary
| Direction in Lyme Disease | ↑ Elevated — higher than in the comparison group |
|---|---|
| Category | Inflammatory |
| Also described as | CC chemokine ligand 19 |
| Compared against | HC (healthy controls) |
| Associated symptoms | Lymphocyte trafficking — research |
| Test type | Blood test (serum / plasma / whole blood) |
| Source | Lantos et al. 2021 — doi:10.1016/j.idc.2021.05.001 |
| Condition atlas | Lyme Disease Biomarker Atlas |
Related Inflammatory markers in Lyme Disease
- C-Reactive Protein (CRP) ↕
- Interferon-γ (IFN-γ) ↑
- Interleukin-10 (IL-10) ↑
- Interleukin-6 (IL-6) ↑
- ESR (erythrocyte sedimentation rate) ↕
Full list: Lyme Disease Biomarker Atlas.
Frequently asked questions
Is CCL19 high or low in Lyme Disease?
Elevated. Studies summarised in the OSMF atlas report higher CCL19 in Lyme Disease than in healthy controls. Source: Lantos et al. 2021.
What symptoms is CCL19 associated with in Lyme Disease?
The cited literature associates this marker with Lymphocyte trafficking — research. These are population-level associations and do not mean the marker causes the symptoms.
Which test measures CCL19?
It is measured as a blood test (serum / plasma / whole blood). Many of the cited studies used research-grade assays, so clinical availability may vary.
Is one abnormal CCL19 result diagnostic of Lyme Disease?
No. No single biomarker is diagnostic of Lyme Disease. CCL19 findings come from group comparisons, overlap considerably between patients and controls, and vary with study design, timing and comparison group. A result should be interpreted by a clinician alongside symptoms, history and other tests.
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Last reviewed: 2026-06-29 · Page generated from lyme.json · Browse: Lyme Disease atlas · Biomarker Index · All marker pages
Disclaimer: This page is an educational synthesis of published, peer-reviewed research and is not medical advice. Biomarker findings vary across studies with case definitions, comparison groups, timing and assay methods. Direction of change reflects the predominant finding in the cited source and does not establish a diagnostic threshold. Discuss any test result with a qualified clinician.