Quantitation of J Chain in Human Biological Fluids by a Simple Immunochemical Procedure

Abstract

ABSTRACT. The molecular form and immunochemical properties of the J chain populations released on reduction and carboxymethylation of normal human plasma, milk, saliva and of plasma containing IgA or IgM M‐components were investigated. A procedure was devised to release the entire J chain population from these various sources and to produce immunochemically identical J chain populations containing only J chain monomers. AH identical standard J chain population was purified and quantitated by physiochemical means. A specific rabbit anti‐J chain antiserum was raised against this pure J chain population. A simple and rapid immunochemical method for J chain quantitation in complex biological fluids as well as in solutions of pure polymeric immunoglobulins was constructed on these grounds. The J chain concentration was found to be (mean +S.D.) 1.74+0.65 μM in normal human plasma, 1.94+1.21 μM. in human milk and 0.48+0.26 +M in human saliva. The J chain/IgA molar ratio was found to be (mean+S.D.) 0.4S+0.07 in human milk and 0.52+0.09 in human saliva when the IgA concentration was expressed as monomeric units per volume unit. The range of the J chain/IgA molar ratios in plasma samples with highly concentrated IgA M‐components was 0‐0.64. The J chain/IgM molar ratio in plasma samples with highly concentrated IgM M‐components was between 1 and 2 when the IgM concentration was expressed as pentameric units per volume unit. 1978 Association for the Publication of the Journal of Internal Medicine