Anti-α-galactosyl antibodies recognizing epitopes terminating with α1,4-linked galactose: Human natural and mouse monoclonal anti-NOR and anti-P1 antibodies

Abstract

The rare NOR erythrocytes, which are agglutinated by most human sera, contain unique glycosphingolipids (globoside elongation products) terminating with the sequence Galα1-4GalNAcβ1-3Gal- recognized by common natural human antibodies. Anti-NOR antibodies were isolated from several human sera by affinity procedures, and their specificity was tested by inhibition of antibody binding to NOR-tripolyacrylamide (PAA) conjugate (ELISA) by the synthetic oligosaccharides, Galα1-4GalNAcβ1-3Gal (NOR-tri), Galα1-4GalNAc (NOR-di), Galα1-4Galβ1-3Galβ1-4Glc ((Gal3Glc), and Galα1-4Gal (P1-di). Two major types of subspecificity of anti-NOR antibodies were found. Type 1 antibodies were found to react strongly with (Gal)3Glc and NOR-tri and weakly with P1-di and NOR-di, which indicated specificity for the trisaccharide epitope Galα1-4Gal/ GalNAcβ1-3Gal. Type 2 antibodies were specific to Galα1-4GalNAc, because they were inhibited most strongly by NOR-tri and NOR-di and were not (or very weakly) inhibited by (Gal)3Glc and P1-di. Monoclonal anti-NOR antibodies were obtained by immunizing mice with NOR-tri-human serum albumin (HSA) conjugate and were found to have type 2 specificity. All anti-NOR antibodies reacted specifically with NOR glycolipids on thin-layer plates. The cross-reactivity of type 1 anti-NOR antibodies with Galα1-4Gal drew attention to a possible antigenic relationship between NOR and blood group P system glycolipids. The latter glycolipids include Pk (Galα1-4Galβ1-4Glc-Cer) present in all normal erythrocytes and P1 (Galα1-4Galβ1-4GlcNAcβ1-3Galβ1-4Glc-Cer) present only in P1 erythrocytes. Sera of some P2 (P1-negative) persons contain natural anti-P1 antibodies. This prompted us to test the specificity of anti-P1 antibodies. Natural human anti-P1 isolated from serum of P2 individual and mouse monoclonal anti-P1 were best inhibited by Galα1-4Galβ1-4GlcNAc (P1-tri) and did not react with NOR-tri and NOR-di. Monoclonal anti-P1 bound to Pk and P1 glycolipids and not to NOR glycolipids. These results indicated an entirely different specificity of anti-NOR and anti-P1 antibodies. Human serum samples differed in the content of anti-α-galactosyl antibodies, including both types of anti-NOR. In the sera of some individuals, type 1 or type 2 anti-NOR antibodies dominated, and other samples contained mixtures of both types of anti-NOR. The biological significance of these new abundant anti-α-galactosyl antibodies still awaits elucidation. © Oxford University Press 2005; all rights reserved.