IgY antiporcine endothelial cell antibodies effectively block human antiporcine xenoantibody binding

被引:34
作者
Fryer, J
Firca, J
Leventhal, J
Blondin, B
Malcolm, A
Ivancic, D
Gandhi, R
Shah, A
Pao, W
Abecassis, M
Kaufman, D
Stuart, F
Anderson, B
机构
[1] Northwestern Univ, Dept Surg, Div Organ Transplantat, Sch Med, Chicago, IL 60611 USA
[2] Ophidian Pharmaceut, Madison, WI USA
[3] Univ Alberta, Dept Lab Med & Pathol, Edmonton, AB, Canada
[4] Northwestern Univ, Sch Med, Chicago, IL 60611 USA
关键词
endothelial activation; endothelial cells; IgY; xenoantibodies; xenotransplantation;
D O I
10.1034/j.1399-3089.1999.00015.x
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Avian IgY antibodies are structurally different from mammalian IgGs and do not fix mammalian complement components or bind human Fc receptors. As these antibody-mediated interactions are believed to play significant roles in both hyperacute rejection (HAR) and acute vascular xenograft rejection (AVXR), IgY antibodies to xenoantigen target epitopes may inhibit these rejection processes. In this report, we show that chicken IgY antibodies to alpha-Gal antigen epitopes and to other porcine aortic endothelial cell (PAEC) antigens block human xenoreactive natural antibody binding to both porcine and rat cardiac tissues and porcine kidney tissues. Chicken IgY antibodies blocked complement-mediated lysis of PAECs by human serum, and inhibited antibody-dependent cell-mediated lysis of PAECs by heat-inactivated human serum plus peripheral blood leukocytes. Binding of IgY to porcine endothelial cells did not affect cell morphology nor expression of E-selectin. These results suggest that avian IgYs could be of potential use in inhibiting pig-to-human xenograft rejection.
引用
收藏
页码:98 / 109
页数:12
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