Literature DB >> 12887109

Evidence for structurally conserved recognition of the major carbohydrate xenoantigen by natural antibodies.

P A Ramsland1, W Farrugia, E Yuriev, A B Edmundson, M S Sandrin.   

Abstract

Natural or preformed antibodies that react with oligosaccharides bearing terminal galactose-alpha(1,3)-galactose [Gal alpha(1,3)Gal] stuctures are present in the sera of all humans. Antibodies against Gal alpha(1,3)Gal epitopes initiate hyperacute rejection of xenografts of porcine organs in human recipients. Despite the enormous clinical potential for xenotransplantation, very little is known about the 3D structural basis for natural antibody recognition of the major xenoantigen (i.e. Gal alpha(1,3)Gal). In this review, we discuss general binding patterns that have been repeatedly identified in antibody complexes with small molecules (haptens), carbohydrate and peptide ligands because similar mechanisms will almost certainly mediate recognition of the major xenoantigen by natural antibodies.

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Year:  2003        PMID: 12887109

Source DB:  PubMed          Journal:  Cell Mol Biol (Noisy-le-grand)        ISSN: 0145-5680            Impact factor:   1.770


  2 in total

1.  The design and synthesis of an α-Gal trisaccharide epitope that provides a highly specific anti-Gal immune response.

Authors:  Kensaku Anraku; Shun Sato; Nicholas T Jacob; Lisa M Eubanks; Beverly A Ellis; Kim D Janda
Journal:  Org Biomol Chem       Date:  2017-04-05       Impact factor: 3.876

2.  Use of molecular modeling and site-directed mutagenesis to define the structural basis for the immune response to carbohydrate xenoantigens.

Authors:  Mary Kearns-Jonker; Natasha Barteneva; Robert Mencel; Namath Hussain; Irina Shulkin; Alan Xu; Margaret Yew; Donald V Cramer
Journal:  BMC Immunol       Date:  2007-03-12       Impact factor: 3.615

  2 in total

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