Soulillou J P, Cantarovich D, Le Mauff B, Giral M, Robillard N, Hourmant M, Hirn M, Jacques Y
Service de Néphrologie et d'Immunologie Clinique, Centre Hospitalier Régional Universitaire, Nantes, France.
N Engl J Med. 1990 Apr 26;322(17):1175-82. doi: 10.1056/NEJM199004263221702.
Interleukin-2 is a major growth factor for activated T lymphocytes, and antibodies reacting with the Tac-chain component of the interleukin-2 receptor can prevent allograft rejection in animals. Because Tac chains are expressed only on a small fraction of activated lymphocytes, monoclonal antibodies against the interleukin-2 receptor may offer a more specific means of immunosuppression than polyclonal antilymphocyte globulin in prophylaxis against graft rejection. Therefore, we compared the immunosuppressive effect of 33B3.1, a rat monoclonal antibody against the human Tac chain, with the effect of a rabbit polyclonal antithymocyte globulin in a randomized study of 100 recipients of first renal transplants. Injections of 33B3.1 (10 mg per day) were tolerated well, whereas major side effects in 15 of 47 patients (32 percent) receiving antithymocyte globulin required discontinuation of treatment before day 14. The incidence of rejection episodes was not statistically different in the two groups at days 14, 30, 60, and 90 after transplantation. Patient and graft survival was also equal in the two groups at one year (96 and 85 percent, respectively, in both groups), and graft function was similar. The total number of infectious episodes within the first three months was lower in the 33B3.1 group than in the antithymocyte group (47 vs. 72). The drop in peripheral-blood lymphocyte concentrations was significantly larger in the patients treated with antithymocyte globulin. The level of circulating Tac-chain-bearing lymphocytes remained below 1 percent during 33B3.1 treatment, as compared with 4 to 5 percent during antithymocyte-globulin treatment (P not significant). We conclude that 33B3.1 is as effective as antithymocyte globulin in the prevention of renal-transplant rejection, and its use results in fewer infections and side effects.
白细胞介素-2是活化T淋巴细胞的主要生长因子,与白细胞介素-2受体的Tac链成分发生反应的抗体可预防动物的同种异体移植排斥反应。由于Tac链仅在一小部分活化淋巴细胞上表达,因此抗白细胞介素-2受体单克隆抗体在预防移植排斥反应方面可能比多克隆抗淋巴细胞球蛋白提供更具特异性的免疫抑制手段。因此,我们在一项对100例首次接受肾移植受者的随机研究中,比较了抗人Tac链大鼠单克隆抗体33B3.1与兔多克隆抗胸腺细胞球蛋白的免疫抑制效果。注射33B3.1(每日10毫克)耐受性良好,而47例接受抗胸腺细胞球蛋白治疗的患者中有15例(32%)出现严重副作用,需要在第14天前停止治疗。移植后第14、30、60和90天,两组排斥反应的发生率无统计学差异。两组患者和移植物的一年生存率也相等(两组均分别为96%和85%),移植物功能相似。33B3.1组前三个月内感染发作的总数低于抗胸腺细胞组(47次对72次)。接受抗胸腺细胞球蛋白治疗的患者外周血淋巴细胞浓度下降明显更大。在33B3.1治疗期间,携带Tac链的循环淋巴细胞水平保持在1%以下,而抗胸腺细胞球蛋白治疗期间为4%至5%(P无显著性差异)。我们得出结论,33B3.1在预防肾移植排斥反应方面与抗胸腺细胞球蛋白一样有效,且使用它导致的感染和副作用更少。