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质粒DNA和mRNA递送:方法与挑战。

Plasmid DNA and mRNA delivery: Approaches and challenges.

作者信息

Singh Arun Kumar, Goel Karan, Dhanawat Meenakshi

机构信息

Department of Pharmacy, Vivekananda Global University, Jaipur, Rajasthan, India.

M.M College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana-Ambala, Haryana, India.

出版信息

Adv Immunol. 2025;165:63-87. doi: 10.1016/bs.ai.2024.12.001. Epub 2025 Apr 13.

Abstract

for delivery of plasmid DNA and mRNA transform biology and medicine, offering powerful tools for gene therapy, vaccine development, cancer immunotherapy, and regenerative medicine. Plasmid DNA provides a relatively stable and sustained expression of the genes which also provides the basic groundwork for long-lasting therapeutic. At the same time, mRNA has also demonstrated more appropriateness for dynamic and time-sensitive applications due to its short-lived and accurate translation capabilities, such as during the development of mRNA-based COVID-19 vaccines. Despite their unique advantages, however, the efficient delivery of these biomolecules poses challenges including immune system activation, enzymatic degradation, and limited cellular uptake. The structural and functional features of plasmid DNA and mRNA highlighted the positive functions that underpin their complementary roles in next-generation biomedical applications. In addition, it highlights the novel delivery routes across lipid nanoparticles, polymeric systems, biomimetic carriers, and hybrid applied sciences which can resolve long-standing challenges to efficient distribution. Emerging technologies such as CRISPR gene editing, self-amplifying RNA, and multiplexed nanoparticles are also increasing the utility of these systems. Significant advances in the delivery of plasmid DNA and mRNA molecules have revolutionized vaccine development, opened new avenues in personalized medicine, and have also inspired a future with engineerable tissues. As these innovations develop, they are predicted to go beyond current limitations and bring around a fresh era of accurate medication taking on one of the global healthcare's most complex challenges. Our revolutionary delivery methods provide stability and simplicity, transforming medical advances.

摘要

用于递送质粒DNA和mRNA可变革生物学和医学,为基因治疗、疫苗开发、癌症免疫治疗和再生医学提供强大工具。质粒DNA能使基因实现相对稳定和持续的表达,这也为持久治疗奠定了基础。同时,mRNA因其寿命短且翻译准确的能力,在动态和对时间敏感的应用中,如在基于mRNA的新冠疫苗开发过程中,也显示出更大的适用性。然而,尽管它们具有独特优势,但这些生物分子的有效递送仍面临挑战,包括免疫系统激活、酶降解和有限的细胞摄取。质粒DNA和mRNA的结构及功能特性凸显了它们在下一代生物医学应用中互补作用的积极功能。此外,它还凸显了脂质纳米颗粒、聚合物系统、仿生载体和混合应用科学等新型递送途径,这些途径可解决高效递送方面长期存在的挑战。CRISPR基因编辑、自扩增RNA和多重纳米颗粒等新兴技术也在增加这些系统的实用性。质粒DNA和mRNA分子递送方面的重大进展彻底改变了疫苗开发,为个性化医疗开辟了新途径,还激发了可工程化组织的未来。随着这些创新的发展,预计它们将突破当前的限制,带来一个精准用药的新时代,应对全球医疗保健最复杂的挑战之一。我们具有革命性的递送方法提供了稳定性和简便性,变革了医学进步。

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