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环孢素(新山地明)与SDZ RAD联合免疫抑制在非人灵长类动物肺移植中的应用:基于药代动力学的系统试验以提高疗效和耐受性。

Combined immunosuppression with cyclosporine (neoral) and SDZ RAD in non-human primate lung transplantation: systematic pharmacokinetic-based trials to improve efficacy and tolerability.

作者信息

Hausen B, Ikonen T, Briffa N, Berry G J, Christians U, Robbins R C, Hook L, Serkova N, Benet L Z, Schuler W, Morris R E

机构信息

Transplantation Immunology, Department of Cardiothoracic Surgery, Stanford University, Palo Alto, CA 94305-5407, USA.

出版信息

Transplantation. 2000 Jan 15;69(1):76-86. doi: 10.1097/00007890-200001150-00015.

Abstract

BACKGROUND

We studied the efficacy and tolerability of combined immunosuppressive therapy with cyclosporine A microemulsion (Neoral) plus the macrolide SDZ RAD 40-0 (2-hydroxyethyl) rapamycin (RAD) in a stringent cynomolgus monkey lung graft model in comparison with cyclosporine or SDZ RAD monotherapy.

METHODS

Thirty-nine cynomolgus monkeys received mixed lymphocyte reaction (MLR) mismatched unilateral lung transplants. Immunosuppressants were administered orally as single daily doses. The observation period was 28 days and follow-up included serial trough blood drug concentrations measured by high performance liquid chromatography/mass spectrometry, blood analyses, chest radiographs, open lung biopsies, as well as tissue drug concentrations and graft histology at necropsy.

RESULTS

Graft biopsies in monkeys treated with vehicle (n=4), Neoral (day 1-7: 150 mg/kg/day; day 8-28: 100 mg/kg/day; n=6; mean +/- SE trough level (MTL): 292+/-17 ng/ml) or SDZ RAD monotherapy (1.5 mg/kg/day; n=6; MTL: 15+/-1 ng/ml) showed severe rejection. Coadministration in two transplant monkeys of Neoral (150/100 mg/kg/day) and SDZ RAD (1.5 mg/kg/day) caused their early death. In both animals, SDZ RAD blood levels were more than 5-fold higher than under monotherapy (MTL: 82+/-18 ng/ml). Simultaneous administration (n=6) of Neoral (150/100 mg/kg/day; MTL: 217+/-16 ng/ml) and SDZ RAD (0.3 mg/kg/day; MTL: 24+/-2 ng/ml) improved graft outcome (mild rejection). Side effects included renal failure (n=2) and seizures (n=1). Three monkeys survived to day 28. In this group the MTL for cyclosporin was 143+/-13 and for RAD 38+/-3. Staggered treatment completely prevented rejection in four of six grafts. However, five of six monkeys had moderate to severe diarrhea. In a concentration-controlled trial of simultaneously administered Neoral and SDZ RAD in transplant monkeys (target SDZ RAD MTL: 20-40 ng/ml; cyclosporine MTL: 100-200 ng/ml) all six monkeys survived with improved drug tolerability and an average biopsy score of mild rejection.

CONCLUSION

Combination of orally administered SDZ RAD and Neoral showed excellent immunosuppressive efficacy in a stringent lung transplant model. The drug interaction and the narrow therapeutic index of this drug combination required careful dose adjustments to optimize tolerability and efficacy.

摘要

背景

我们在一个严格的食蟹猴肺移植模型中,研究了环孢素A微乳剂(新山地明)联合大环内酯类药物SDZ RAD 40-0(2-羟乙基雷帕霉素,RAD)与环孢素或SDZ RAD单药治疗相比的疗效和耐受性。

方法

39只食蟹猴接受了混合淋巴细胞反应(MLR)不匹配的单侧肺移植。免疫抑制剂作为每日单次剂量口服给药。观察期为28天,随访包括通过高效液相色谱/质谱法测量的系列谷血药浓度、血液分析、胸部X光片、开放性肺活检,以及尸检时的组织药物浓度和移植物组织学检查。

结果

接受赋形剂治疗的猴子(n = 4)、新山地明治疗的猴子(第1 - 7天:150 mg/kg/天;第8 - 28天:100 mg/kg/天;n = 6;平均±标准误谷浓度(MTL):292 ± 17 ng/ml)或SDZ RAD单药治疗的猴子(1.5 mg/kg/天;n = 6;MTL:15 ± 1 ng/ml)的移植肺活检显示严重排斥反应。两只移植猴同时给予新山地明(150/100 mg/kg/天)和SDZ RAD(1.5 mg/kg/天)导致它们早期死亡。在这两只动物中,SDZ RAD血药浓度比单药治疗时高5倍以上(MTL:82 ± 18 ng/ml)。同时给予新山地明(150/100 mg/kg/天;MTL:217 ± 16 ng/ml)和SDZ RAD(0.3 mg/kg/天;MTL:24 ± 2 ng/ml)可改善移植肺结局(轻度排斥反应)。副作用包括肾衰竭(n = 2)和癫痫发作(n = 1)。三只猴子存活至第28天。在该组中,环孢素的MTL为143 ± 13,RAD的MTL为38 ± 3。错开给药完全预防了6个移植肺中的4个发生排斥反应。然而,6只猴子中有5只出现中度至重度腹泻。在一项对移植猴同时给予新山地明和SDZ RAD的浓度控制试验中(目标SDZ RAD MTL:20 - 40 ng/ml;环孢素MTL:100 - 200 ng/ml),所有6只猴子均存活,药物耐受性改善,平均活检评分为轻度排斥反应。

结论

在严格的肺移植模型中,口服SDZ RAD和新山地明联合显示出优异的免疫抑制疗效。这种药物组合的药物相互作用和狭窄的治疗指数需要仔细调整剂量以优化耐受性和疗效。

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