Xenotransplantation: in vitro analysis of synthetic alpha-galactosyl inhibitors of human anti-Galalpha1-->3Gal IgM and IgG antibodies

• Published in: Glycobiology (Oxford) 2000-02, Vol.10 (2), p.141-148
• Main Authors: Rieben, R, Bovin, N V, Korchagina, E Y, Oriol, R, Nifant'ev, N E, Tsvetkov, D E, Daha, M R, Mohacsi, P J, Joziasse, D H
• Format: Article
• Language: English
• Subjects: Animals; Antibodies, Heterophile - immunology; Carbohydrate Sequence; Cell Line; Disaccharides - immunology; Disaccharides - pharmacology; Glycoconjugates - chemical synthesis; Glycoconjugates - chemistry; Glycoconjugates - pharmacology; Humans; Immunoglobulin G - immunology; Immunoglobulin M - immunology; Molecular Sequence Data; Oligosaccharides - chemical synthesis; Oligosaccharides - chemistry; Oligosaccharides - pharmacology; Structure-Activity Relationship; Swine; Transplantation, Heterologous - immunology; Trisaccharides - pharmacology
• ISSN: 0959-6658; 1460-2423; 1460-2423
• DOI: 10.1093/glycob/10.2.141

Pig-to-human xenotransplantation might be an option to overcome the increasing shortage of human donor organs. However, naturally occurring antibodies in human blood against the Galalpha1-->3Gal antigen on pig endothelial cells lead to hyperacute or, if prevented, acute or delayed vascular rejection of the pig graft. The purpose of this study was therefore to evaluate synthetic oligosaccharides with terminal Galalpha1-->3Gal to inhibit antigen-binding and cytotoxicity of anti-alphaGal antibodies against pig cells. Different oligosaccharides were synthesized chemically and by a combined chemico-enzymatic approach. These included monomeric di-, tri-, and pentasaccharides, a polyacrylamide-conjugate (PAA-Bdi), as well as di-, tetra-, and octamers of Galalpha1-->3Gal. All were tested for inhibitory activity by anti-alphaGal ELISA and complement-dependent cytotoxicity tests. PAA-Bdi was the best inhibitor of binding as well as cytotoxicity of anti-alphaGal antibodies. Monomeric oligosaccharides efficiently prevented binding of anti-alphaGal IgG, but less well that of anti-alphaGal IgM, with tri- and pentasaccharides showing a better efficacy than the disaccharide. The two trisaccharides Galalpha1-->3Galbeta1-->4GlcNAc and Galalpha1-->3Galbeta1-->3GlcNAc were equally effective. Oligomers of Galalpha1-->3Gal were more effective than monomers in blocking the binding of anti-alphaGal IgG. However, they could not block IgM binding, nor could they match the efficacy of PAA-Bdi. We conclude that oligosaccharides with terminal Galalpha1-->3Gal, most effectively as PAA-conjugates, can prevent binding and cytotoxicity of human anti-alphaGal in vitro. The PAA-Bdi conjugate might be most suited for use as a Sepharose-bound immunoabsorption material.