Dong Xiaojuan, Hara Hidetaka, Wang Ying, Wang Li, Zhang Yingnan, Cooper David K C, Dai Yifan, Pan Zhiqiang
Beijing Ophthalmology & Visual Science Key Laboratory, BeijingTongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Department of Surgery, Thomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, PA, USA.
Xenotransplantation. 2017 Jan;24(1). doi: 10.1111/xen.12282. Epub 2017 Jan 5.
To investigate graft survival after full-thickness corneal xenotransplantation from α1,3-galactosyltransferase gene-knockout (GTKO) pigs expressing a human complement regulatory protein (GTKO/CD46 pigs) in rhesus monkeys.
Rhesus monkeys (n=10) were transplanted with full-thickness corneas from wild-type (WT; n=4) and GTKO/CD46 (n=4) pigs or from monkeys (n=2). All recipient monkeys received post-transplant subconjunctival injections of betamethasone. Corneal grafts were evaluated by slit-lamp. Histopathology, immunohistochemistry of the grafts, and cytokine concentrations in the aqueous humor were tested 6 months after transplantation. Anti-pig IgM/IgG and anti-galactose-α1,3-galactose (Gal) antibodies were determined by flow cytometry and ELISA, respectively.
The longest graft survival of WT and GTKO/CD46 xenografts was 157 and 171 days, respectively. There was no significant difference in graft survival between WT and GTKO pig corneas. Anterior synechiae occurred in two recipients of WT and all recipients of GTKO/CD46 grafts. All xenograft recipients developed a retrocorneal membrane, inflammatory cells (CD3 T lymphocytes) infiltrated the corneal stroma, and in the aqueous humor, IL-6 was increased 6 months after transplantation. Induced antibody responses were documented against Gal and/or non-Gal pig antigens. In contrast, allografts survived >180 days without any rejection, with no increase in cytokines in the aqueous humor, and no elicited serum anti-pig antibodies were detected.
α1,3-galactosyltransferase gene-knockout/CD46 pig corneas were not associated with prolonged graft survival or a reduced antibody response compared with WT pig corneas. The prevention of the development of anterior synechiae and a retrocorneal membrane after corneal xenotransplantation would appear to be important if prolonged corneal xenograft survival is to be achieved.
研究在恒河猴中,来自表达人补体调节蛋白的α1,3-半乳糖基转移酶基因敲除(GTKO)猪(GTKO/CD46猪)的全层角膜异种移植后的移植物存活情况。
将10只恒河猴分别移植来自野生型(WT;n = 4)和GTKO/CD46(n = 4)猪或来自猴子(n = 2)的全层角膜。所有受体猴在移植后接受结膜下注射倍他米松。通过裂隙灯评估角膜移植物。移植6个月后测试移植物的组织病理学、免疫组织化学以及房水中的细胞因子浓度。分别通过流式细胞术和酶联免疫吸附测定法测定抗猪IgM/IgG和抗半乳糖-α1,3-半乳糖(Gal)抗体。
WT和GTKO/CD46异种移植物的最长移植物存活时间分别为157天和171天。WT和GTKO猪角膜之间的移植物存活情况无显著差异。前粘连发生在2只接受WT移植物的受体和所有接受GTKO/CD46移植物的受体中。所有异种移植受体均形成角膜后膜,炎性细胞(CD3 T淋巴细胞)浸润角膜基质,并且在移植6个月后房水中白细胞介素-6升高。记录到针对Gal和/或非Gal猪抗原的诱导抗体反应。相比之下,同种异体移植物存活超过180天且无任何排斥反应,房水中细胞因子未增加,并且未检测到引发的血清抗猪抗体。
与WT猪角膜相比,α1,3-半乳糖基转移酶基因敲除/CD46猪角膜与延长移植物存活时间或降低抗体反应无关。如果要实现角膜异种移植移植物的长期存活,预防角膜异种移植后前粘连和角膜后膜的形成似乎很重要。