Department of Formulation Development, ReNAP Therapeutics, Tehran, Iran.
Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
J Nanobiotechnology. 2022 Jun 14;20(1):276. doi: 10.1186/s12951-022-01478-7.
In the last decade, the development of messenger RNA (mRNA) therapeutics by lipid nanoparticles (LNP) leads to facilitate clinical trial recruitment, which improves the efficacy of treatment modality to a large extent. Although mRNA-LNP vaccine platforms for the COVID-19 pandemic demonstrated high efficiency, safety and adverse effects challenges due to the uncontrolled immune responses and inappropriate pharmacological interventions could limit this tremendous efficacy. The current study reveals the interplay of immune responses with LNP compositions and characterization and clarifies the interaction of mRNA-LNP therapeutics with dendritic, macrophages, neutrophile cells, and complement. Then, pharmacological profiles for mRNA-LNP delivery, including pharmacokinetics and cellular trafficking, were discussed in detail in cancer types and infectious diseases. This review study opens a new and vital landscape to improve multidisciplinary therapeutics on mRNA-LNP through modulation of immunopharmacological responses in clinical trials.
在过去的十年中,脂质纳米粒(LNP)介导的信使 RNA(mRNA)疗法的发展促进了临床试验的招募,在很大程度上提高了治疗方式的疗效。尽管用于 COVID-19 大流行的 mRNA-LNP 疫苗平台表现出高效、安全性和不良反应挑战,由于不受控制的免疫反应和不当的药理学干预可能限制这种巨大的疗效。本研究揭示了免疫反应与 LNP 组成和特性的相互作用,并阐明了 mRNA-LNP 治疗剂与树突状细胞、巨噬细胞、嗜中性粒细胞和补体的相互作用。然后,详细讨论了包括药代动力学和细胞内转运在内的 mRNA-LNP 传递的药理学特征,包括在癌症类型和传染病中的特征。这项综述研究为通过在临床试验中调节免疫药理学反应来改善基于 mRNA-LNP 的多学科治疗开辟了一个新的重要领域。