Summary
| Direction in Lyme Disease | ↕ Inconsistent — reported as both higher and lower across studies, with no consistent direction |
|---|---|
| Category | Chronic/PTLDS |
| Also described as | B-cell chemokine |
| Compared against | HC, treated Lyme (healthy controls, treated Lyme) |
| Associated symptoms | Persistent symptoms research |
| Test type | Blood test (serum / plasma / whole blood) |
| Source | Aucott et al. 2014 — doi:10.1016/j.amjmed.2014.02.016 |
| Condition atlas | Lyme Disease Biomarker Atlas |
Related Chronic/PTLDS markers in Lyme Disease
Full list: Lyme Disease Biomarker Atlas.
Frequently asked questions
Is Serum CXCL13 (PTLDS research) high or low in Lyme Disease?
Mixed. Some studies report higher and others lower Serum CXCL13 (PTLDS research) in Lyme Disease compared with healthy controls, treated Lyme, so no single direction is established. Source: Aucott et al. 2014.
What symptoms is Serum CXCL13 (PTLDS research) associated with in Lyme Disease?
The cited literature associates this marker with Persistent symptoms research. These are population-level associations and do not mean the marker causes the symptoms.
Which test measures Serum CXCL13 (PTLDS research)?
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 Serum CXCL13 (PTLDS research) result diagnostic of Lyme Disease?
No. No single biomarker is diagnostic of Lyme Disease. Serum CXCL13 (PTLDS research) 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.