Fig. 3.
Selective retention of natural IgG autoantibody activity by IVIgM coupled to Sepharose. IVIg (50 mg) was subjected to affinity chromatography on 60 mg of IVIgM coupled to Sepharose. The acid-eluted fraction of the column (▪) and the loaded material (□) were then compared for reactivity with a panel of self (TG, MG, and TF ) and non-self (PLD and PK) antigens by ELISA.