The mechanism of IgA deposition in the kidneys in IgA nephropathy is unknown, Mesangial IgA is of the IgA I subclass, and since no consistent antigenic target for the IgA I has been described, we have investigated the glycosylation of the molecule, as a potential non‐immunological abnormality which may contribute to its deposition. IgA 1 is rich in carbohydrate, carrying N‐linked moieties in common with IgG, but also O‐linked sugars, which are rare in serum proteins, and not expressed by IgG or lgA2, Lectin binding assays were designed to examine the expression of terminal galactose on the N‐linked carbohydrate chains of purified serum IgG and IgAI, and the O‐linked sugars of IgAI and C1 inhibitor (one of the very few other serum proteins with O‐linked glycosylation). No evidence was found for abnormalities of N‐linked glycosylation of either isotype in IgA nephropathy compared with matched controls. However, in IgA nephropathy, reduced terminal galactosylation of the hinge region O‐linked moieties was demonstrated; this was not seen in C1 inhibitor, which showed normal or increased galactosylation of the O‐linked sugars. This abnormality of IgA1 has considerable implications for the pathogenesis of IgA nephropathy, since the O‐linked sugars lie in an important functional location within the IgA1 molecule, close to the ligand of Fc receptors. Changes in the carbohydrates in this site may therefore affect interactions with receptors and extracellular proteins, leading to anomalous handling of the IgA1 protein in this condition, including failure of normal clearance mechanisms, and mesangial deposition.