Monoclonal
immunoglobulins (
M-components) in blood are found in some patients with
polyneuropathy and are thought to be of pathogenetic importance, especially if the M-component is of
IgM isotype. As the finding of an M-component may indicate a treatable
polyneuropathy, the potential of the method to uncover an M-component is of importance.
Cellulose acetate or
agarose electrophoresis used in routine practice may miss small
M-components covered by other
proteins. We therefore applied the uncovering and specific method of immunofixation in comparison with
agarose electrophoresis on patients investigated for
polyneuropathy. Of 83 consecutive patients, 5 had
M-components. Two of these 5 patients, one with an axonal
polyneuropathy and the other with a lower motor neuron syndrome, had extra bands on
agarose electrophoresis, verified as
IgG M-components by immunofixation. In the 3 additional patients an M-component was uncovered only by immunofixation, not seen in the
agarose electrophoresis of plasma; 2 of them were of
IgM isotype and one was of
IgG isotype. These 3 patients were diagnosed as having a demyelinating (i.e., possibly immune-mediated)
polyneuropathy by means of neurophysiology and in one by means of nerve biopsy. A 6th patient had 2 small bands in the gamma region on the
agarose electrophoresis, verified as
oligoclonal bands of
IgG isotype by immunofixation but was not judged as an M-component. Three out of the 83 patients, were judged as having
motor neuron diseases. All remaining 80 were found to have
polyneuropathy.(ABSTRACT TRUNCATED AT 250 WORDS)