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OKT3首剂反应:与T细胞亚群及细胞因子释放的关联

OKT3 first-dose reaction: association with T cell subsets and cytokine release.

作者信息

Gaston R S, Deierhoi M H, Patterson T, Prasthofer E, Julian B A, Barber W H, Laskow D A, Diethelm A G, Curtis J J

机构信息

Department of Medicine, University of Alabama, Birmingham.

出版信息

Kidney Int. 1991 Jan;39(1):141-8. doi: 10.1038/ki.1991.18.

DOI:10.1038/ki.1991.18
PMID:1900552
Abstract

Use of the monoclonal antibody OKT3 to prevent or treat allograft rejection has become commonplace. Its administration is often complicated by serious side effects, usually occurring within one to two hours after OKT3 is given, and is termed first-dose reaction. The mechanism underlying these signs and symptoms is poorly defined, but may be related to cytokine release. Twenty-three kidney or kidney/pancreas transplant recipients received OKT3 as treatment of acute rejection. Signs and symptoms occurring after the first dose were observed and quantitated prospectively, and a reaction score was calculated. Blood was drawn immediately before, and at 2 and 24 hours after the first dose of OKT3 for determination of interleukin-2 (IL2), interferon-gamma (IFN gamma), and tumor necrosis factor-alpha (TNF alpha) levels, and flow cytometric analysis of T cell subsets. Two groups were defined based on severity of first-dose reaction. Group 1 patients (N = 11) had very mild reactions (reaction score less than or equal to 3); Group 2 patients (N = 12) had more severe reactions (score greater than or equal to 5). All patients demonstrated a significant rise in serum TNF alpha from baseline to two hours after OKT3 (9 +/- 3 pg/ml to 378 +/- 54 pg/ml, P less than 0.0001), and there was significant correlation between reaction scores and two-hour TNF alpha levels (P = 0.005). Group 2 patients had higher TNF alpha levels at two hours than did Group 1 patients (484 +/- 75 pg/ml vs. 263 +/- 62 pg/ml, P = 0.04). Levels of IL2 and IFN gamma were not elevated at any sampling time.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

使用单克隆抗体OKT3预防或治疗同种异体移植排斥反应已变得很常见。其给药常常因严重副作用而变得复杂,这些副作用通常在给予OKT3后一到两小时内出现,被称为首剂反应。这些体征和症状的潜在机制尚不清楚,但可能与细胞因子释放有关。23名肾或肾/胰腺移植受者接受OKT3治疗急性排斥反应。前瞻性观察并量化首剂后出现的体征和症状,并计算反应评分。在首剂OKT3给药前、给药后2小时和24小时立即采血,以测定白细胞介素-2(IL2)、干扰素-γ(IFNγ)和肿瘤坏死因子-α(TNFα)水平,并对T细胞亚群进行流式细胞术分析。根据首剂反应的严重程度定义了两组。第1组患者(N = 11)有非常轻微的反应(反应评分小于或等于3);第2组患者(N = 12)有更严重的反应(评分大于或等于5)。所有患者血清TNFα从基线到OKT3给药后2小时均显著升高(9±3 pg/ml至378±54 pg/ml,P < 0.0001),反应评分与2小时TNFα水平之间存在显著相关性(P = 0.005)。第2组患者2小时时的TNFα水平高于第1组患者(484±75 pg/ml对263±62 pg/ml,P = 0.04)。在任何采样时间,IL2和IFNγ水平均未升高。(摘要截短于250字)

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OKT3 first-dose reaction: association with T cell subsets and cytokine release.OKT3首剂反应:与T细胞亚群及细胞因子释放的关联
Kidney Int. 1991 Jan;39(1):141-8. doi: 10.1038/ki.1991.18.
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In vivo cell activation following OKT3 administration. Systemic cytokine release and modulation by corticosteroids.注射OKT3后体内细胞的激活。全身细胞因子的释放及皮质类固醇的调节作用。
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J Urol. 1991 May;145(5):928-31. doi: 10.1016/s0022-5347(17)38493-8.
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Immunologic monitoring with Orthoclone OKT3 therapy.使用Orthoclone OKT3疗法进行免疫监测。
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Treatment of acute cellular rejection with T10B9.1A-31 or OKT3 in renal allograft recipients.肾移植受者中使用T10B9.1A - 31或OKT3治疗急性细胞排斥反应。
Transplantation. 1992 Jan;53(1):80-6. doi: 10.1097/00007890-199201000-00015.
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A randomized prospective trial of low-dose OKT3 induction therapy to prevent rejection and minimize side effects in recipients of kidney transplants.一项关于低剂量OKT3诱导疗法预防肾移植受者排斥反应并将副作用降至最低的随机前瞻性试验。
Transplantation. 2000 Jun 15;69(11):2374-81. doi: 10.1097/00007890-200006150-00027.
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Pentoxifylline does not prevent the cytokine-induced first dose reaction following OKT3--a randomized, double-blind placebo-controlled study.己酮可可碱不能预防OKT3治疗后细胞因子诱导的首剂反应——一项随机、双盲、安慰剂对照研究。
Transplantation. 1996 Feb 27;61(4):573-7. doi: 10.1097/00007890-199602270-00010.

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