Higginbotham Laura, Mathews Dave, Breeden Cynthia A, Song Mingqing, Farris Alton Brad, Larsen Christian P, Ford Mandy L, Lutz Andrew J, Tector Matthew, Newell Kenneth A, Tector A Joseph, Adams Andrew B
Department of Surgery, Emory Transplant Center, Emory University School of Medicine, Atlanta, GA, USA.
Anatomic Pathology, Emory University School of Medicine, Atlanta, GA, USA.
Xenotransplantation. 2015 May-Jun;22(3):221-30. doi: 10.1111/xen.12166. Epub 2015 Apr 3.
Xenotransplantation has the potential to alleviate the organ shortage that prevents many patients with end-stage renal disease from enjoying the benefits of kidney transplantation. Despite significant advances in other models, pig-to-primate kidney xenotransplantation has met limited success. Preformed anti-pig antibodies are an important component of the xenogeneic immune response. To address this, we screened a cohort of 34 rhesus macaques for anti-pig antibody levels. We then selected animals with both low and high titers of anti-pig antibodies to proceed with kidney transplant from galactose-α1,3-galactose knockout/CD55 transgenic pig donors. All animals received T-cell depletion followed by maintenance therapy with costimulation blockade (either anti-CD154 mAb or belatacept), mycophenolate mofetil, and steroid. The animal with the high titer of anti-pig antibody rejected the kidney xenograft within the first week. Low-titer animals treated with anti-CD154 antibody, but not belatacept exhibited prolonged kidney xenograft survival (>133 and >126 vs. 14 and 21 days, respectively). Long-term surviving animals treated with the anti-CD154-based regimen continue to have normal kidney function and preserved renal architecture without evidence of rejection on biopsies sampled at day 100. This description of the longest reported survival of pig-to-non-human primate kidney xenotransplantation, now >125 days, provides promise for further study and potential clinical translation.
异种移植有潜力缓解器官短缺问题,而这种短缺使许多终末期肾病患者无法受益于肾移植。尽管在其他模型上取得了重大进展,但猪到灵长类动物的肾异种移植取得的成功有限。预先形成的抗猪抗体是异种免疫反应的重要组成部分。为了解决这一问题,我们对34只恒河猴进行了抗猪抗体水平筛查。然后,我们选择了抗猪抗体滴度低和高的动物,用半乳糖-α1,3-半乳糖敲除/CD55转基因猪供体进行肾移植。所有动物均接受T细胞清除,随后用共刺激阻断剂(抗CD154单克隆抗体或贝拉西普)、霉酚酸酯和类固醇进行维持治疗。抗猪抗体滴度高的动物在第一周内排斥了肾异种移植物。用抗CD154抗体治疗的低滴度动物,而非用贝拉西普治疗的动物,肾异种移植物存活时间延长(分别为>133天和>126天,而对照组为14天和21天)。用基于抗CD154方案治疗的长期存活动物肾功能持续正常,肾结构保持完整,在第100天采集的活检样本中没有排斥反应的迹象。目前猪到非人灵长类动物肾异种移植最长存活时间>125天的这一描述,为进一步研究和潜在的临床转化带来了希望。