Gaber A O, Thistlethwaite J R, Haag B W, Stuart J K, Mayes J T, Lloyd D M, Fellner S, Stuart F P
Am Surg. 1987 Jul;53(7):407-9.
With the introduction of more potent immunosuppressive regimens, increasing numbers of kidney transplant recipients traditionally viewed as being at high immunologic risk for rejection and graft loss have been accepted. These include recipients of multiple grafts, sensitized patients as measured by high panel reactive antibody (PRA), and patients with current warm B or historical positive crossmatches. Since November 1983, all recipients of cadaver kidneys have been treated with cyclosporine and prednisone. In addition, most also received a short posttransplant course of antilymphocyte globulin and long-term azathioprine. With these regimens, retransplantation, sensitization, current B-cell crossmatch and historical B- and/or T-cell crossmatch do not affect graft survival.
随着更有效的免疫抑制方案的引入,越来越多传统上被视为免疫排斥和移植肾丢失高风险的肾移植受者被纳入接受移植。这些受者包括多次移植的患者、通过高群体反应性抗体(PRA)检测为致敏的患者以及当前存在B细胞交叉配型阳性或既往有T细胞交叉配型阳性的患者。自1983年11月以来,所有尸体肾移植受者均接受环孢素和泼尼松治疗。此外,大多数患者还在移植后接受了短疗程的抗淋巴细胞球蛋白治疗以及长期的硫唑嘌呤治疗。采用这些方案后,再次移植、致敏状态、当前的B细胞交叉配型以及既往的B细胞和/或T细胞交叉配型均不影响移植肾存活。