Barr M L, Meiser B M, Eisen H J, Roberts R F, Livi U, Dall'Amico R, Dorent R, Rogers J G, Radovancević B, Taylor D O, Jeevanandam V, Marboe C C
Department of Surgery of the University of Southern California, Los Angeles 90033, USA.
N Engl J Med. 1998 Dec 10;339(24):1744-51. doi: 10.1056/NEJM199812103392404.
Photopheresis is an immunoregulatory technique in which lymphocytes are reinfused after exposure to a photoactive compound (methoxsalen) and ultraviolet A light. We performed a preliminary study to assess the safety and efficacy of photopheresis in the prevention of acute rejection of cardiac allografts.
A total of 60 consecutive eligible recipients of primary cardiac transplants were randomly assigned to standard triple-drug immunosuppressive therapy (cyclosporine, azathioprine, and prednisone) alone or in conjunction with photopheresis. The photopheresis group received a total of 24 photopheresis treatments, each pair of treatments given on two consecutive days, during the first six months after transplantation. The regimen for maintenance immunosuppression, the definition and treatment of rejection episodes, the use of prophylactic antibiotics, and the schedule for cardiac biopsies were standardized among all 12 study centers. All the cardiac-biopsy samples were graded in a blinded manner at a central pathology laboratory. Plasma from the subgroup of 34 patients (57 percent) who were enrolled at the nine U.S. centers was analyzed by polymerase-chain-reaction amplification for cytomegalovirus DNA.
After six months of follow-up, the mean (+/-SD) number of episodes of acute rejection per patient was 1.44+/-1.0 in the standard-therapy group, as compared with 0.91+/-1.0 in the photopheresis group (P=0.04). Significantly more patients in the photopheresis group had one rejection episode or none (27 of 33) than in the standard-therapy group (14 of 27), and significantly fewer patients in the photopheresis group had two or more rejection episodes (6 of 33) than in the standard-therapy group (13 of 27, P=0.02). There was no significant difference in the time to a first episode of rejection, the incidence of rejection associated with hemodynamic compromise, or survival at 6 and 12 months. Although there were no significant differences in the rates or types of infection, cytomegalovirus DNA was detected significantly less frequently in the photopheresis group than in the standard-therapy group (P=0.04).
In this pilot study, the addition of photopheresis to triple-drug immunosuppressive therapy significantly decreased the risk of cardiac rejection without increasing the incidence of infection.
光化学疗法是一种免疫调节技术,淋巴细胞在暴露于光活性化合物(甲氧沙林)和紫外线A光后被重新注入体内。我们进行了一项初步研究,以评估光化学疗法在预防心脏同种异体移植急性排斥反应中的安全性和有效性。
总共60例连续符合条件的原发性心脏移植受者被随机分配至单独接受标准三联药物免疫抑制治疗(环孢素、硫唑嘌呤和泼尼松)或联合光化学疗法。光化学疗法组在移植后的前六个月共接受24次光化学疗法治疗,每两次治疗连续进行两天。所有12个研究中心的维持免疫抑制方案、排斥反应发作的定义和治疗、预防性抗生素的使用以及心脏活检的时间表均标准化。所有心脏活检样本均在中央病理实验室以盲法分级。对在美国9个中心入组的34例患者(57%)亚组的血浆进行聚合酶链反应扩增分析,以检测巨细胞病毒DNA。
随访六个月后,标准治疗组患者急性排斥反应发作的平均(±标准差)次数为1.44±1.0,而光化学疗法组为0.91±1.0(P = 0.04)。光化学疗法组有一次或无排斥反应发作的患者(33例中的27例)明显多于标准治疗组(27例中的14例),光化学疗法组有两次或更多次排斥反应发作的患者(33例中的6例)明显少于标准治疗组(27例中的13例,P = 0.02)。首次排斥反应发作的时间、与血流动力学损害相关的排斥反应发生率或6个月和12个月时的生存率无显著差异。虽然感染率和感染类型无显著差异,但光化学疗法组巨细胞病毒DNA的检测频率明显低于标准治疗组(P = 0.04)。
在这项初步研究中,三联药物免疫抑制治疗联合光化学疗法可显著降低心脏排斥反应的风险,而不增加感染发生率。