Goss J A, Finke E H, Flye M W, Lacy P E
Department of Surgery, Washington University School of Medicine, St. Louis, Missouri 63110.
J Clin Invest. 1994 Mar;93(3):1312-4. doi: 10.1172/JCI117088.
Streptozotocin-induced, diabetic mice (C57BL/6) were preimmunized by injecting 25 low temperature, cultured Wistar-Furth (WF) rat islets into the portal vein, and the recipients received one injection of mouse and rat antilymphocyte sera. 3 wk later, fresh WF islets were transplanted under the kidney capsule of the preimmunized recipients, and normoglycemia was maintained in all 13 recipients for 60 d. Removal of the grafts at 60 d returned the mice to a diabetic state. Transplants of fresh WF islets under the kidney capsule without pretreatment of the recipients had a mean survival time of 16.5 +/- 2.5 d. These findings demonstrate that immune unresponsiveness can be achieved across a concordant, islet xenograft barrier within 3 wk after intrahepatic preimmunization with a small number of donor rat islets and transient immunosuppression with antilymphocyte sera.
用链脲佐菌素诱导的糖尿病小鼠(C57BL/6)通过向门静脉注射25个低温培养的Wistar-Furth(WF)大鼠胰岛进行预免疫,受体接受一次小鼠和大鼠抗淋巴细胞血清注射。3周后,将新鲜的WF胰岛移植到预免疫受体的肾包膜下,所有13只受体均维持正常血糖60天。60天时移除移植物使小鼠恢复糖尿病状态。未对受体进行预处理而将新鲜WF胰岛移植到肾包膜下,其平均存活时间为16.5±2.5天。这些发现表明,在用少量供体大鼠胰岛进行肝内预免疫并使用抗淋巴细胞血清进行短暂免疫抑制后3周内,可跨越协调性胰岛异种移植屏障实现免疫无反应性。