کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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4262306 | 1284604 | 2008 | 4 صفحه PDF | دانلود رایگان |
BackgroundTo avoid hyperacute rejection of xeno-organs, α1,3-galactosyltransferase knock-out (GalT-KO) pigs have been produced. However, Galα1,3Gal (Gal) determinant elimination may expose cryptic carbohydrate antigens and/or generate new antigens that might interfere with the human immune response.MethodsGlycolipids isolated from small intestine and pancreas of two GalT-KO and one wild-type (WT) pig were tested for immune reactivity with antibodies on thin-layer chromatograms after separation by high-performance liquid chromatography, and selected fractions were analysed by proton NMR spectroscopy.ResultsImmunostaining using purified human anti-Gal Abs revealed that tissues from WT animals express large amounts of Gal-antigens whereas GalT-KO tissues lacked these antigens. Proton NMR spectroscopy on small intestine fractions revealed both linear and branched nona- and decaglycosylceramides, respectively, with terminal Gal-epitopes. In corresponding GalT-KO fractions, Gal-epitopes seemed to be replaced by terminal α1,2fucoses. Two novel branched blood group H compounds was found in the GalT-KO intestine.ConclusionsThe structural complexity of αGal-terminating antigens in the WT organs is very high. Knockout of α1,3GalT by gene-targeting results in elimination of Gal-determinants. In addition structurally novel α1,2fucose-terminated blood group H compounds were identified in the GalT-KO tissue. These compounds are not expected to be recognized by the human immune system.
Journal: Transplantation Proceedings - Volume 40, Issue 2, March 2008, Pages 543–546