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外周动脉疾病生物疗法临床前试验中高龄与动脉粥样硬化的转化相关性

Translational Relevance of Advanced Age and Atherosclerosis in Preclinical Trials of Biotherapies for Peripheral Artery Disease.

作者信息

Webster Keith A

机构信息

Vascular Biology Institute, University of Miami, Miami, FL 33146, USA.

Department of Ophthalmology, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Genes (Basel). 2024 Jan 22;15(1):135. doi: 10.3390/genes15010135.

Abstract

Approximately 6% of adults worldwide suffer from peripheral artery disease (PAD), primarily caused by atherosclerosis of lower limb arteries. Despite optimal medical care and revascularization, many PAD patients remain symptomatic and progress to critical limb ischemia (CLI) and risk major amputation. Delivery of pro-angiogenic factors as proteins or DNA, stem, or progenitor cells confers vascular regeneration and functional recovery in animal models of CLI, but the effects are not well replicated in patients and no pro-angiogenic biopharmacological procedures are approved in the US, EU, or China. The reasons are unclear, but animal models that do not represent clinical PAD/CLI are implicated. Consequently, it is unclear whether the obstacles to clinical success lie in the toxic biochemical milieu of human CLI, or in procedures that were optimized on inappropriate models. The question is significant because the former case requires abandonment of current strategies, while the latter encourages continued optimization. These issues are discussed in the context of relevant preclinical and clinical data, and it is concluded that preclinical mouse models that include age and atherosclerosis as the only comorbidities that are consistently present and active in clinical trial patients are necessary to predict clinical success. Of the reviewed materials, no biopharmacological procedure that failed in clinical trials had been tested in animal models that included advanced age and atherosclerosis relevant to PAD/CLI.

摘要

全球约6%的成年人患有外周动脉疾病(PAD),主要由下肢动脉粥样硬化引起。尽管接受了最佳的医疗护理和血管重建治疗,但许多PAD患者仍有症状,并进展为严重肢体缺血(CLI),面临重大截肢风险。在CLI动物模型中,递送作为蛋白质或DNA的促血管生成因子、干细胞或祖细胞可实现血管再生和功能恢复,但这些效果在患者中并未得到很好的重现,且在美国、欧盟或中国,尚无促血管生成生物药理学程序获得批准。原因尚不清楚,但可能与未代表临床PAD/CLI的动物模型有关。因此,目前尚不清楚临床应用失败的原因是在于人类CLI的毒性生化环境,还是在于在不适当模型上优化的程序。这个问题很重要,因为如果是前一种情况,就需要放弃当前的策略,而后一种情况则鼓励继续优化。本文结合相关临床前和临床数据对这些问题进行了讨论,并得出结论,要预测临床应用的成功,需要建立临床前小鼠模型,该模型要将年龄和动脉粥样硬化作为唯一始终存在且在临床试验患者中活跃的合并症。在所审查的资料中,没有一种在临床试验中失败的生物药理学程序在包含与PAD/CLI相关的高龄和动脉粥样硬化的动物模型中进行过测试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94bb/10815340/ed636e78bba3/genes-15-00135-g001.jpg

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