Quantitative Immunoturbidimetry
Kappa free light chains (kFLCs) in cerebrospinal fluid (CSF) are used in the diagnostic evaluation of multiple sclerosis (MS) as markers of intrathecal immunoglobulin synthesis. Excess light chains are produced during inflammatory activity in the central nervous system (CNS).
The 2024 McDonald criteria recognize kFLCs as an acceptable alternative to oligoclonal bands (OCBs) for establishing a positive CSF result. Compared with OCB testing, kFLC measurement is faster, less labor-intensive, and more objective.
Disease Overview
MS is a chronic immune-mediated disease of the CNS characterized by inflammation and demyelination. Diagnosis is based on the McDonald criteria, which incorporate clinical findings, imaging, and laboratory evidence of intrathecal inflammation.
Indications for Use
This test is used to evaluate patients with suspected MS.
Test Interpretation
Results
Results reflect CSF-specific immunoglobulin synthesis.
| Result | Value | Additional Information |
|---|---|---|
| Negative | <0.33 mg/L | Not suggestive of intrathecal inflammation; oligoclonal banding is not indicated |
| Equivocal | 0.33 mg/L–1.09 mg/L | May be consistent with intrathecal inflammation; consider additional CSF testing (e.g., Oligoclonal Band Profile 0080440) |
| Positive | >1.09 mg/L | Consistent with intrathecal inflammation; consider additional CSF testing (e.g., Oligoclonal Band Profile 0080440) |
Limitations
kFLCs are not specific to MS and may be elevated in other neurologic conditions, including autoimmune, infectious, inflammatory, cerebrovascular, and paraneoplastic disorders. Additional CSF testing (e.g., oligoclonal banding) may be warranted based on the clinical context.
Related Tests
This test measures CSF kFLCs only. ARUP also offers CSF Kappa Free Light Chains With Reflex to Oligoclonal Banding (3021031) and Oligoclonal Band Profile (0080440).
References
-
40975101
Montalban X, Lebrun-Frénay C, Oh J, et al. Diagnosis of multiple sclerosis: 2024 revisions of the McDonald criteria. Lancet Neurol. 2025;24(10):850-865.

