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用OKT3治疗类固醇抵抗性肾移植排斥反应。

OKT3 treatment of steroid-resistant renal allograft rejection.

作者信息

Thistlethwaite J R, Gaber A O, Haag B W, Aronson A J, Broelsch C E, Stuart J K, Stuart F P

出版信息

Transplantation. 1987 Feb;43(2):176-84. doi: 10.1097/00007890-198702000-00003.

Abstract

The monoclonal antibody, Orthoclone OKT3 (OKT3), has been used with great efficacy in a prospective multicenter trial as therapy for first rejection episodes in cadaveric donor (CD) renal allograft recipients treated with azathioprine (AZA) and prednisone (P). However, although almost all rejection episodes were reversed, recurrent rejection occurred in approximately two-thirds of OKT3-treated patients in this earlier trial; infections also occurred in about two-thirds of patients, often related to the additional immunosuppression necessary to reverse the rerejection episodes. In the current series of patients, OKT3 was used to treat rejection in CD renal graft recipients in a protocol differing from the multicenter trial in two respects: baseline immunosuppression was cyclosporine (CsA) and P or CsA, AZA, and P (probably more potent immunosuppressive combinations than the AZA and P in the multicenter trial); and OKT3 treatment was reserved for rejection episodes resistant to 3 bolus infusions of methylprednisolone (MP), 5-10 mg/kg, rather than as primary therapy for first rejection episodes. Using this protocol, 46 of 74 rejection episodes (62%) diagnosed between 3/85 and 3/86 in CD renal allograft recipients were treated successfully with MP. Of the remaining 28 steroid-resistant rejection episodes, 27 (96%) were reversed with a 7-14-day course of OKT3, 5 mg/day. Only 5 recurrent rejection episodes (19%) have been observed in the 2-14-month follow-up period after OKT3 treatment; infections have occurred in 10 patients (36%), and three grafts (11%) have been lost in OKT3 treated patients. These results suggest that recurrent rejection and subsequent infection after OKT3 is used to treat rejection may be reduced in a protocol where CD renal allograft recipients are treated with baseline immunosuppression regimens including CsA and where OKT3 is reserved for steroid-resistant rejection. This approach appears to be both more cost-effective than, and as effective therapeutically as, treating all first rejection episodes with the monoclonal antibody.

摘要

单克隆抗体Orthoclone OKT3(OKT3)在一项前瞻性多中心试验中,作为接受硫唑嘌呤(AZA)和泼尼松(P)治疗的尸体供体(CD)肾移植受者首次排斥反应的治疗方法,疗效显著。然而,尽管几乎所有的排斥反应都得到了逆转,但在这项早期试验中,约三分之二接受OKT3治疗的患者出现了反复排斥反应;约三分之二的患者也发生了感染,这通常与逆转再次排斥反应所需的额外免疫抑制有关。在当前的一系列患者中,OKT3用于治疗CD肾移植受者的排斥反应,其方案在两个方面与多中心试验不同:基线免疫抑制为环孢素(CsA)和P或CsA、AZA和P(可能比多中心试验中的AZA和P具有更强的免疫抑制组合);OKT3治疗仅用于对3次大剂量静脉注射甲泼尼龙(MP)(5-10mg/kg)耐药的排斥反应,而不是作为首次排斥反应的主要治疗方法。采用该方案,在1985年3月至1986年3月期间诊断出的74例CD肾移植受者的排斥反应中,46例(62%)经MP成功治疗。在其余28例对类固醇耐药的排斥反应中,27例(96%)经7-14天的OKT3(5mg/天)疗程逆转。在OKT3治疗后的2-14个月随访期内,仅观察到5例反复排斥反应(19%);10例患者(36%)发生了感染,3例移植肾(11%)在接受OKT3治疗的患者中丢失。这些结果表明,在采用包括CsA的基线免疫抑制方案治疗CD肾移植受者且OKT3仅用于类固醇耐药排斥反应的方案中,使用OKT3治疗排斥反应后反复排斥反应和随后感染的发生率可能会降低。这种方法似乎比用单克隆抗体治疗所有首次排斥反应更具成本效益,且治疗效果相同。

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