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TNF-α 阻断在已建立的多囊肾病动物模型中无效。

TNF-α blockade is ineffective in animal models of established polycystic kidney disease.

机构信息

Biomed Valley Discoveries Inc, 4520 Main Street, Suite 1650, MO 64111, Kansas City, USA.

出版信息

BMC Nephrol. 2013 Oct 25;14:233. doi: 10.1186/1471-2369-14-233.

Abstract

BACKGROUND

Given the large medical burden of polycystic kidney disease (PKD) and recent clinical trial failures, there is a need for novel, safe and effective treatments for the disorder.

METHODS

In PCK rat and PKD2(ws25/w183) mouse models, entanercept was administered once every three days at 5 or 10 mg/kg, once daily. Mozavaptan was administered as a pilot control, provided continuously via milled chow at 0.1%. Animals were assessed for measures of pharmacodynamic response, and improvements in measures of polycystic kidney disease.

RESULTS

Entanercept treatment modulated inflammatory markers, but provided limited therapeutic benefit in multiple animal models of established polycystic kidney disease. Kidney weight, cyst burden and renal function markers remained unchanged following administration of etanercept at various dose levels and multiple treatment durations.

CONCLUSIONS

While it remains possible that TNF-α inhibition may be effective in truly preventative settings, our observations suggest this pathway is less likely to exhibit therapeutic or disease-modifying efficacy following the standard clinical diagnosis of disease.

摘要

背景

鉴于多囊肾病(PKD)的巨大医疗负担和最近临床试验的失败,我们需要一种新的、安全有效的治疗方法。

方法

在 PCK 大鼠和 PKD2(ws25/w183)小鼠模型中,依那西普每三天给药一次,剂量为 5 或 10mg/kg,每天一次。莫扎伐普坦作为先导对照药物,通过粉碎的饲料以 0.1%的浓度持续给药。评估动物的药效反应和多囊肾病的改善情况。

结果

依那西普治疗可调节炎症标志物,但在多种已建立的多囊肾病动物模型中,提供的治疗益处有限。在不同剂量水平和多种治疗持续时间下,依那西普给药后,肾脏重量、囊肿负担和肾功能标志物均无变化。

结论

虽然 TNF-α 抑制在真正的预防环境中可能仍然有效,但我们的观察结果表明,在疾病的标准临床诊断后,该途径不太可能表现出治疗或疾病修饰的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d34/4231369/a35865db4da0/1471-2369-14-233-1.jpg

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