What is it about?

New biologic therapies use monoclonal antibodies, that can be confounded for an endogenous monoclonal protein on protein electrophoresis and immunofixation.

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Why is it important?

We describe a method that could help differentiate between an endogenous monoclonal protein and a therapeutic monoclonal antibody, using mass spectrometry. That could decrease unnecessary tests and worries from patients.

Perspectives

The field of therapeutic monoclonal antibodies is growing and there will be more and more of these therapies that may impact laboratory test results for patients undergoing therapy with these drugs. In the field of myeloma, that will be particularly important since patients with myeloma are monitored using protein electrophoresis and immunofixation while on therapy with monoclonal antibodies, so distinguishing between residual disease and visualization of the drug is extremely important. This study focuses on more common mAbs, used for autoimmune inflammatory disorders. Patients taking these drugs not always have electrophoresis done as part of their routine monitoring, but when they do, and we see the therapeutic mAb migrating on the gel and report that as a monoclonal protein, that may create unnecessary anxiety and further investigations for a monoclonal gammopathy of undetermined significance, amyloidosis, or other diseases. The method our group developed may help clarify whether the protein is endogenous or therapy, and states at which concentrations there may be an issue.

Dr Maria Alice V Willrich
Mayo Clinic

Read the Original

This page is a summary of: Monoclonal antibody therapeutics as potential interferences on protein electrophoresis and immunofixation, Clinical Chemistry and Laboratory Medicine (CCLM), January 2016, De Gruyter,
DOI: 10.1515/cclm-2015-1023.
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