Monoclonal IgM cryoglobulinemia associated with gamma‐3 heavy chain disease: immunochemical and biochemical studies

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Abstract
A patient (Mia) with a monoclonal IgM(k) cryoglobulin (cryo IgM) developed additional heavy chain disease proteins of the γ3 subclass 8 years later. Biochemical studies of the cryo IgM indicated that the heavy chain was VHI, but the NH2‐terminal amino acid sequence of the light chain did not permit a definite assignment of its VK subgroup. Two major fragments of the γ3 chain were distinguishable by electrophoresis in sodium dodecyl sulfate polyacryl‐amide gel. The smaller component (designated Mia F) had a molecular weight of approximately 30 000 and the larger component (designated Mia S) 35 000. Both fragments had G3m(21) and G3m(27) allotypic determinants. These data and the NH2‐terminal amino acid sequence of the γ chain fragments suggested that Mia S consists of the major part of the γ3 hinge region plus the CH2 and CH3 domains of the γ3 chain, whereas Mia F may be derived from the former as a result of postsynthetic cleavage. The partial amino acid sequence of the Mia S fragment is homologous to the hinge region amino acid sequence of human γ3 chains reported in the literature, with only one amino acid difference out of the 11 residues compared. This difference may represent an allotypic difference within the γ3 subclass. Alternatively, the production of Mia S may have resulted from the accidental derepression of a “silent” constant region gene not expressed in normal individuals.
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