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脂质纳米颗粒包裹的mRNA治疗药物和疫苗的药代动力学建模:一项系统综述。

Pharmacometric modeling of lipid nanoparticle-encapsulated mRNA therapeutics and vaccines: A systematic review.

作者信息

Zhang Miao, Van Linh, Amiji Mansoor M

机构信息

Moderna Therapeutics, 325 Binney Street, Cambridge, MA 02142, USA.

Department of Pharmaceutical Sciences, School of Pharmacy, Bouvé College of Health Sciences, Northeastern University, Boston, MA 02115, USA.

出版信息

Mol Ther Nucleic Acids. 2025 Aug 14;36(3):102686. doi: 10.1016/j.omtn.2025.102686. eCollection 2025 Sep 9.

Abstract

Significant progress has been made in the development of lipid nanoparticle (LNP)-encapsulated messenger RNA (mRNA)-based modalities with numerous candidates entering clinical trials. These novel modalities require the application of innovative quantitative models to inform the development of mRNA-LNP-based candidates. To this end, we conducted a comprehensive search of registered clinical trials related to mRNA-based modalities on ClinicalTrials.gov, summarizing the current advancements of mRNA-LNP-based modalities and their expanding therapeutic applications. Also, we performed a thorough review of quantitative models related to mRNA-LNP-based modalities from PubMed, Google Scholar, and Embase databases, exploring the model structures employed to capture the processes of mRNA-LNP, along with their current applications. Between 2002 and October 28, 2024, around 189 clinical trials were registered on ClinicalTrials.gov, encompassing approximately 132 unique mRNA-based modalities targeting 18 disease areas. There are 15 studies that have published quantitative models supporting both the preclinical and clinical development of mRNA-LNP-based therapeutics. Detail regarding quantitative modeling of mRNA-LNP, especially absorption, distribution, metabolism, and excretion, as well as the activation processes of immune responses induced by mRNA-LNP-based vaccines are reviewed. Furthermore, we offer insights for future research related to mRNA-LNP-related models, aimed at enhancing predictive performance and facilitating the expedited advancement of mRNA-LNP-related clinical development.

摘要

在脂质纳米颗粒(LNP)包裹的信使核糖核酸(mRNA)疗法的开发方面已经取得了重大进展,众多候选药物进入了临床试验阶段。这些新型疗法需要应用创新的定量模型,以为基于mRNA-LNP的候选药物的开发提供信息。为此,我们在ClinicalTrials.gov上对与基于mRNA的疗法相关的注册临床试验进行了全面搜索,总结了基于mRNA-LNP的疗法的当前进展及其不断扩大的治疗应用。此外,我们对来自PubMed、谷歌学术和Embase数据库的与基于mRNA-LNP的疗法相关的定量模型进行了全面回顾,探索了用于描述mRNA-LNP过程的模型结构及其当前应用。在2002年至2024年10月28日期间,ClinicalTrials.gov上登记了约189项临床试验,涵盖了针对18个疾病领域的约132种独特的基于mRNA的疗法。有15项研究发表了支持基于mRNA-LNP的疗法临床前和临床开发的定量模型。本文综述了mRNA-LNP定量建模的细节,特别是吸收、分布、代谢和排泄,以及基于mRNA-LNP的疫苗诱导的免疫反应激活过程。此外,我们为与mRNA-LNP相关模型的未来研究提供了见解,旨在提高预测性能并促进基于mRNA-LNP的临床开发的加速推进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc1c/12418826/22e87dd50c8e/fx1.jpg

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