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Monitoring free light chains in serum using mass spectrometry

  • David R. Barnidge EMAIL logo , Angela Dispenzieri , Giampaolo Merlini , Jerry A. Katzmann and David L. Murray
Published/Copyright: February 4, 2016

Abstract

Background: Serum immunoglobulin free light chains (FLC) are secreted into circulation by plasma cells as a by-product of immunoglobulin production. In a healthy individual the population of FLC is polyclonal as no single cell is secreting more FLC than the total immunoglobulin secreting cell population. In a person with a plasma cell dyscrasia, such as multiple myeloma (MM) or light chain amyloidosis (AL), a clonal population of plasma cells secretes a monoclonal light chain at a concentration above the normal polyclonal background.

Methods: We recently showed that monoclonal immunoglobulin rapid accurate mass measurement (miRAMM) can be used to identify and quantify a monoclonal light chain (LC) in serum and urine above the polyclonal background. This was accomplished by reducing immunoglobulin disulfide bonds releasing the LC to be analyzed by microLC-ESI-Q-TOF mass spectrometry. Here we demonstrate that the methodology can also be applied to the detection and quantification of FLC by analyzing a non-reduced sample.

Results: Proof of concept experiments were performed using purified FLC spiked into normal serum to assess linearity and precision. In addition, a cohort of 27 patients with AL was analyzed and miRAMM was able to detect a monoclonal FLC in 23 of the 27 patients that had abnormal FLC values by immunonephelometry.

Conclusions: The high resolution and high mass measurement accuracy provided by the mass spectrometry based methodology eliminates the need for κ/λ ratios as the method can quantitatively monitor the abundance of the κ and λ polyclonal background at the same time it measures the monoclonal FLC.


Corresponding author: Dr. David R. Barnidge, Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 1st St SW, Rochester, MN 55905, USA, Phone: +(507) 266-4777

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Received: 2015-9-20
Accepted: 2015-12-27
Published Online: 2016-2-4
Published in Print: 2016-6-1

©2016 by De Gruyter

Articles in the same Issue

  1. Frontmatter
  2. Editorial
  3. Protein electrophoresis and serum free light chains in the diagnosis and monitoring of plasma cell disorders: laboratory testing and current controversies
  4. Laboratory Testing as Recommended by the Guidelines and the International Myeloma Working Group
  5. Laboratory testing requirements for diagnosis and follow-up of multiple myeloma and related plasma cell dyscrasias
  6. Free light chain testing for the diagnosis, monitoring and prognostication of AL amyloidosis
  7. Laboratory testing in monoclonal gammopathy of renal significance (MGRS)
  8. The impact of renal function on the clinical performance of FLC measurement in AL amyloidosis
  9. Serum and Urine Protein Electrophoresis and Immunofixation Testing
  10. Challenges of measuring monoclonal proteins in serum
  11. Screening immunofixation should replace protein electrophoresis as the initial investigation of monoclonal gammopathy: Point
  12. Should routine laboratories stop doing screening serum protein electrophoresis and replace it with screening immune-fixation electrophoresis? No quick fixes: Counterpoint
  13. Moving towards harmonized reporting of serum and urine protein electrophoresis
  14. Multiple qualitative and quantitative methods for free light chain analysis are necessary as first line tests for AL amyloidosis
  15. Use of isoelectric focusing to discriminate transient oligoclonal bands from monoclonal protein in treated myeloma
  16. New patterns of relapse in multiple myeloma: a case of “light chain escape” in which FLC predicted relapse earlier than urine and serum immunofixation
  17. Serum Free Light Chain Methods and Controversies
  18. Analytical issues of serum free light chain assays and the relative performance of polyclonal and monoclonal based reagents
  19. Measurement of free light chains with assays based on monoclonal antibodies
  20. Measurement of free light chains – pros and cons of current methods
  21. Is accuracy of serum free light chain measurement achievable?
  22. Performance goals for immunoglobulins and serum free light chain measurements in plasma cell dyscrasias can be based on biological variation
  23. A patient with AL amyloidosis with negative free light chain results
  24. Strengths and weaknesses of methods for identifying monoclonal free light chains of Ig: examples from two cases with renal disease
  25. Comparison of Freelite™ and N Latex serum free light chain assays in subjects with end stage kidney disease on haemodialysis
  26. New Laboratory Assays and Challenges
  27. Quantification of β-region IgA monoclonal proteins – should we include immunochemical Hevylite® measurements? Point
  28. Quantification of β region IgA paraproteins – should we include immunochemical “heavy/light chain” measurements? Counterpoint
  29. Free light chains and heavy/light chains in monitoring POEMS patients
  30. Monitoring free light chains in serum using mass spectrometry
  31. Monoclonal antibody therapeutics as potential interferences on protein electrophoresis and immunofixation
  32. Monitoring multiple myeloma patients treated with daratumumab: teasing out monoclonal antibody interference
  33. Interference of daratumumab in monitoring multiple myeloma patients using serum immunofixation electrophoresis can be abrogated using the daratumumab IFE reflex assay (DIRA)
  34. Letter to the Editor
  35. Discrepancy between FLC assays: only a problem of quantification?
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