Webster A, Pankhurst T, Rinaldi F, Chapman J R, Craig J C
Children's Hospital at Westmead, Centre for Kidney Research, Locked Bag 4001, Westmead, NSW, Australia, 2145.
Cochrane Database Syst Rev. 2006 Apr 19(2):CD004756. doi: 10.1002/14651858.CD004756.pub3.
Registry data shows that between 15-35% kidney recipients will undergo treatment for at least one episode of acute rejection within the first post transplant year. Treatment options include pulsed steroid therapy, the use of an antibody preparation, the alteration of background immunosuppression, or combinations of these options. In 2002, in the US, 61.4% patients with an acute rejection episode received steroids, 20.4% received an antibody preparation and 18.2% received both.
To determine the benefits and harms of mono- or polyclonal antibodies (Ab) used to treat acute rejection in kidney transplant recipients.
We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (in The Cochrane Library, issue 2, 2005), MEDLINE (1966-June 2005), EMBASE (1980-June 2005), and the specialised register of the Cochrane Renal Group (June 2005).
Randomised controlled trials (RCTs) in all languages comparing all mono- and polyclonal antibody preparations, given in combination with any other immunosuppressive agents, for the treatment of acute graft rejection, when compared to any other treatment for acute rejection.
Two reviewers independently assessed trials for eligibility and quality, and extracted data. Results are expressed as relative risk (RR) with 95% confidence intervals (CI).
Twenty one trials (49 reports, 1387 patients) were identified. Trials were generally small, incompletely reported, especially for potential harms, and did not define outcome measures adequately. Fourteen trials (965 patients) compared therapies for first rejection episodes. Ab was better than steroid in reversing rejection (RR 0.57, 95% CI 0.38 to 0.87) and preventing graft loss (death censored RR 0.74, CI 0.58 to 0.95) but there was no difference in preventing subsequent rejection or death at one year. Seven trials (422 patients) investigated Ab treatment of steroid-resistant rejection. There was no benefit of muromonab-CD3 over ATG or ALG in either reversing rejection, preventing subsequent rejection, preventing graft loss or death.
AUTHORS' CONCLUSIONS: In reversing first rejection, any antibody is better than steroid and also prevents graft loss, but subsequent rejection and patient survival are not significantly different. In reversing steroid-resistant rejection the effects of different antibodies are also not significantly different. Given the clinical problem caused by acute rejection, data are very sparse, and clinically important differences in outcomes between widely used interventions have not been excluded. Standardised reproducible outcome criteria are needed.
登记数据显示,15%至35%的肾移植受者在移植后的第一年内将因至少一次急性排斥反应而接受治疗。治疗选择包括脉冲式类固醇疗法、使用抗体制剂、改变基础免疫抑制方案或这些方案的联合使用。2002年,在美国,61.4%发生急性排斥反应的患者接受了类固醇治疗,20.4%接受了抗体制剂治疗,18.2%两者都接受了。
确定用于治疗肾移植受者急性排斥反应的单克隆或多克隆抗体的益处和危害。
我们检索了Cochrane对照试验中心注册库(CENTRAL)(Cochrane图书馆2005年第2期)、MEDLINE(1966年至2005年6月)、EMBASE(1980年至2005年6月)以及Cochrane肾脏组的专业注册库(2005年6月)。
所有语言的随机对照试验(RCT),比较所有单克隆和多克隆抗体制剂与任何其他免疫抑制剂联合使用治疗急性移植物排斥反应时,与急性排斥反应的任何其他治疗方法相比。
两名评价员独立评估试验的合格性和质量,并提取数据。结果以相对风险(RR)及95%置信区间(CI)表示。
共识别出21项试验(49份报告,1387例患者)。试验规模通常较小,报告不完整,尤其是关于潜在危害方面,且未充分定义结局指标。14项试验(965例患者)比较了首次排斥反应发作的治疗方法。抗体在逆转排斥反应(RR 0.57,95%CI 0.38至0.87)和预防移植物丢失(死亡删失RR 0.74,CI 0.58至0.95)方面优于类固醇,但在预防随后的排斥反应或一年时的死亡方面无差异。7项试验(422例患者)研究了抗体治疗类固醇抵抗性排斥反应。在逆转排斥反应、预防随后的排斥反应、预防移植物丢失或死亡方面,莫罗单抗-CD3并不优于抗胸腺细胞球蛋白(ATG)或抗淋巴细胞球蛋白(ALG)。
在逆转首次排斥反应方面,任何抗体均优于类固醇,且能预防移植物丢失,但随后的排斥反应和患者生存率无显著差异。在逆转类固醇抵抗性排斥反应方面,不同抗体的效果也无显著差异。鉴于急性排斥反应所导致的临床问题,数据非常稀少,且尚未排除广泛使用的干预措施在结局方面的临床重要差异。需要标准化且可重复的结局标准。