*Department of Surgery, Thomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, PA; †Department of Pathology, University of Pittsburgh, Pittsburgh, PA; and ‡Revivicor, Inc, Blacksburg, VA.
Cornea. 2014 Apr;33(4):390-7. doi: 10.1097/ICO.0000000000000069.
The aim of this study was to investigate the distribution of antigens other than galactose-α-1,3-galactose (Gal) (non-Gal) recognized by human and rhesus monkey serum antibodies in the α-1,3-galactosyltransferase gene-knockout (GTKO) pig cornea.
The distribution of non-Gal, specifically N-glycolylneuraminic acid (NeuGc), in the corneas from wild-type (WT) and GTKO pigs was identified. Corneal sections from WT and GTKO pigs were incubated with human or rhesus monkey serum to determine immunoglobulin (Ig)M and IgG binding to corneal tissue by means of fluorescent microscopy.
Strong expression of NeuGc was found in all layers of both WT and GTKO pig corneas. In both humans and monkeys, antibody binding (IgG > IgM) to GTKO was found to be weaker than that to entire WT pig corneas, but in both, most antibody binding, especially IgG, was to the epithelium. There was weak diffuse antibody binding, especially of IgG, to the corneal stroma, suggesting binding to antigens expressed on collagen. There was no or minimal binding of IgM/IgG to the corneal endothelium.
Although the cornea is avascular, antibodies in primate serum can bind to pig antigens, especially on epithelial cells and stromal collagen. Although the binding to entire GTKO corneas was weaker than that to WT corneas, deletion of the expression of NeuGc and expression of human complement-regulatory proteins in the pig cornea will be important if prolonged clinical corneal xenograft survival is to be achieved.
本研究旨在研究人类和恒河猴血清抗体识别的除半乳糖-α-1,3-半乳糖(Gal)(非-Gal)以外的抗原在α-1,3-半乳糖基转移酶基因敲除(GTKO)猪角膜中的分布。
鉴定了野生型(WT)和 GTKO 猪角膜中非-Gal(特别是 N-羟乙酰神经氨酸(NeuGc))的分布。用人类或恒河猴血清孵育 WT 和 GTKO 猪的角膜切片,通过荧光显微镜确定免疫球蛋白(Ig)M 和 IgG 与角膜组织的结合。
在 WT 和 GTKO 猪角膜的所有层中均发现了强烈表达的 NeuGc。在人类和猴子中,与 GTKO 的抗体结合(IgG>IgM)均弱于与整个 WT 猪角膜的结合,但在两者中,大多数抗体结合,尤其是 IgG,都发生在上皮细胞。角膜基质中有较弱的弥散性抗体结合,尤其是 IgG,提示与胶原上表达的抗原结合。角膜内皮细胞无或仅有微量的 IgM/IgG 结合。
尽管角膜是无血管的,但在灵长类动物血清中的抗体可以与猪抗原结合,特别是在上皮细胞和基质胶原上。尽管与整个 GTKO 角膜的结合弱于与 WT 角膜的结合,但在猪角膜中删除 NeuGc 的表达和表达人补体调节蛋白将是实现延长临床角膜异种移植物存活时间的重要因素。