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肌小管肌病临床前模型中的疾病进展的自然史研究和统计建模。

Natural history study and statistical modeling of disease progression in a preclinical model of myotubular myopathy.

机构信息

Dynacure, Illkirch 67400, France.

Pharmalex, Mont-St-Guibert 1435, Belgium.

出版信息

Dis Model Mech. 2022 Jul 1;15(7). doi: 10.1242/dmm.049284. Epub 2022 Jul 25.

DOI:10.1242/dmm.049284
PMID:35642830
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9346515/
Abstract

Generating reliable preclinical data in animal models of disease is essential in therapy development. Here, we performed statistical analysis and joint longitudinal-survival modeling of the progressive phenotype observed in Mtm1-/y mice, a reliable model for myotubular myopathy. Analysis of historical data was used to generate a model for phenotype progression, which was then confirmed with phenotypic data from a new colony of mice derived via in vitro fertilization in an independent animal house, highlighting the reproducibility of disease phenotype in Mtm1-/y mice. These combined data were used to refine the phenotypic parameters analyzed in these mice and improve the model generated for expected disease progression. The disease progression model was then used to test the therapeutic efficacy of Dnm2 targeting. Dnm2 reduction by antisense oligonucleotides blocked or postponed disease development, and resulted in a significant dose-dependent improvement outside the expected disease progression in untreated Mtm1-/y mice. This provides an example of optimizing disease analysis and testing therapeutic efficacy in a preclinical model, which can be applied by scientists testing therapeutic approaches using neuromuscular disease models in different laboratories. This article has an associated First Person interview with the joint first authors of the paper.

摘要

在疾病的动物模型中生成可靠的临床前数据对于治疗开发至关重要。在这里,我们对 Mtm1-/y 小鼠中观察到的进行性表型进行了统计分析和联合纵向生存建模,Mtm1-/y 小鼠是肌小管肌病的可靠模型。对历史数据的分析用于生成表型进展模型,然后使用通过体外受精在独立动物房中产生的新小鼠群体的表型数据进行验证,突出了 Mtm1-/y 小鼠中疾病表型的可重复性。这些组合数据用于改进对这些小鼠进行分析的表型参数,并改进为预期疾病进展生成的模型。然后使用疾病进展模型来测试 Dnm2 靶向的治疗效果。反义寡核苷酸降低 Dnm2 可阻止或延迟疾病发展,并导致未治疗的 Mtm1-/y 小鼠的预期疾病进展之外的显著剂量依赖性改善。这为优化临床前模型中的疾病分析和测试治疗效果提供了一个例子,这可以为使用不同实验室的神经肌肉疾病模型测试治疗方法的科学家提供参考。本文附有对该论文的共同第一作者的第一人称采访。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/473e/9346515/3566ba05bbd6/dmm-15-049284-g6.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/473e/9346515/dfd0b97de217/dmm-15-049284-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/473e/9346515/3566ba05bbd6/dmm-15-049284-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/473e/9346515/1726bb040109/dmm-15-049284-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/473e/9346515/b00d3721ea2f/dmm-15-049284-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/473e/9346515/60babf0f5a1d/dmm-15-049284-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/473e/9346515/3ba2c6e95eb4/dmm-15-049284-g4.jpg
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本文引用的文献

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Dis Model Mech. 2022 Jul 1;15(7). doi: 10.1242/dmm.049342. Epub 2022 Jul 25.
2
Re: "Moving Forward After Two Deaths in a Gene Therapy Trial of Myotubular Myopathy" by Wilson and Flotte.回复:威尔逊和弗洛特所著的《在肌管性肌病基因治疗试验中两例死亡事件后继续前行》
Hum Gene Ther. 2020 Aug;31(15-16):787. doi: 10.1089/hum.2020.217.
3
Myostatin: a Circulating Biomarker Correlating with Disease in Myotubular Myopathy Mice and Patients.肌生成抑制素:一种与肌管性肌病小鼠及患者疾病相关的循环生物标志物。
X 连锁肌小管肌病与表观遗传改变有关,并可通过 HDAC 抑制得到改善。
Acta Neuropathol. 2022 Sep;144(3):537-563. doi: 10.1007/s00401-022-02468-7. Epub 2022 Jul 17.
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Natural history of a mouse model of X-linked myotubular myopathy.X 连锁肌小管肌病小鼠模型的自然病史。
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Improving translatability of preclinical studies for neuromuscular disorders: lessons from the TREAT-NMD Advisory Committee for Therapeutics (TACT).提高神经肌肉疾病临床前研究的可翻译性:TREAT-NMD 治疗咨询委员会 (TACT) 的经验教训。
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