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Production of human monoclonal antibodies against Galα(1–3)Gal
Author(s) -
Wittig Olga,
Taylor Peter,
Montaño Ramón,
Alonso José,
Romano Egidio
Publication year - 2002
Publication title -
xenotransplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.052
H-Index - 61
eISSN - 1399-3089
pISSN - 0908-665X
DOI - 10.1034/j.1399-3089.2002.01032.x
Subject(s) - monoclonal antibody , epitope , antibody , xenotransplantation , microbiology and biotechnology , isotype , phage display , hybridoma technology , chemistry , biology , transplantation , immunology , medicine , surgery
The hyperacute rejection observed in models of pig‐to‐human xenotransplantation is mainly because of the presence of natural antibodies in human blood with specificity for the Galα(1–3)Gal (Gal) carbohydrate moiety present on the surface of porcine endothelial cells. Human monoclonal anti‐Gal antibodies could be of use both in the study of the basic mechanisms of hyperacute rejection as well as in its clinical prevention. In the present study we prepared 42 heterohybridomas (human–mouse) secreting antibodies with specificity for the Gal epitope. All of the antibodies produced were of the IgM isotype, according to a dot‐blot assay. Twenty‐seven antibodies were further characterized, and shown to be specific for Gal by different methods, including an enzyme‐linked immunosorbent assay, in which the plates were sensitized with mouse laminin as a source of Gal. Specificity was also confirmed using purified Gal carbohydrate in a hemagglutination inhibition assay. The antibodies were shown to mediate lysis of Gal‐expressing rabbit erythrocytes in the presence of complement. However, the heterohybridomas themselves were shown to express Gal, a result of the mouse P3x63Ag8.653 hybridoma cells used during hybridoma generation. The presence of this epitope on the surface of anti‐Gal‐producing cells, and on the antibody itself, represents a limitation to the production of high affinity anti‐Gal antibodies.