Protein is expressed in all major organs after intravenous infusion of mRNA-lipid nanoparticles in swine

IF 4.6 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Molecular Therapy-Methods & Clinical Development Pub Date : 2024-08-06 DOI:10.1016/j.omtm.2024.101314
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Abstract

In vivo delivery of mRNA is promising for the study of gene expression and the treatment of diseases. Lipid nanoparticles (LNP) enable efficient delivery of mRNA constructs, but protein expression has been assumed to be limited to the liver. With specialized LNP, delivery to extrahepatic tissue occurs in small animal models, however it is unclear if global delivery of mRNA to all major organs is possible in humans, because delivery may be affected by differences in innate immune response and relative organ size. Furthermore, limited studies with LNP have been performed in large animal models, such as swine, due to their sensitivity to complement activation-related pseudoallergy (CARPA). In this study, we found that exogenous protein expression occurred in all major organs when swine were injected intravenously with a relatively low dose of mRNA encapsulated in a clinically relevant LNP formulation. Exogenous protein was detected in the liver, spleen, lung, heart, uterus, colon, stomach, kidney, small intestine, and brain of the swine without inducing CARPA. Furthermore, protein expression was detected in the bone marrow, including megakaryocytes, hematopoietic stem cells, granulocytes, and in circulating white blood cells and platelets. These results show that nearly all major organs contain exogenous protein expression and are viable targets for mRNA therapies.

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猪静脉注射 mRNA 脂质纳米颗粒后,蛋白质在所有主要器官中均有表达
在体内输送 mRNA 有助于研究基因表达和治疗疾病。脂质纳米颗粒(LNP)能有效地传递 mRNA 构建体,但蛋白质的表达一直被认为仅限于肝脏。在小型动物模型中,使用专门的 LNP 可以将 mRNA 运送到肝外组织,但目前还不清楚人类是否可以将 mRNA 全面运送到所有主要器官,因为运送可能会受到先天性免疫反应差异和相对器官大小的影响。此外,由于猪对补体活化相关假过敏(CARPA)的敏感性,在猪等大型动物模型中进行的 LNP 研究十分有限。在这项研究中,我们发现给猪静脉注射相对低剂量的封装在临床相关 LNP 配方中的 mRNA 时,所有主要器官都会出现外源蛋白表达。在猪的肝、脾、肺、心脏、子宫、结肠、胃、肾、小肠和大脑中都检测到了外源性蛋白,而不会诱发 CARPA。此外,在骨髓(包括巨核细胞、造血干细胞、粒细胞)以及循环白细胞和血小板中也检测到了蛋白表达。这些结果表明,几乎所有主要器官都含有外源蛋白表达,是 mRNA 疗法的可行靶点。
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来源期刊
Molecular Therapy-Methods & Clinical Development
Molecular Therapy-Methods & Clinical Development Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.90
自引率
4.30%
发文量
163
审稿时长
12 weeks
期刊介绍: The aim of Molecular Therapy—Methods & Clinical Development is to build upon the success of Molecular Therapy in publishing important peer-reviewed methods and procedures, as well as translational advances in the broad array of fields under the molecular therapy umbrella. Topics of particular interest within the journal''s scope include: Gene vector engineering and production, Methods for targeted genome editing and engineering, Methods and technology development for cell reprogramming and directed differentiation of pluripotent cells, Methods for gene and cell vector delivery, Development of biomaterials and nanoparticles for applications in gene and cell therapy and regenerative medicine, Analysis of gene and cell vector biodistribution and tracking, Pharmacology/toxicology studies of new and next-generation vectors, Methods for cell isolation, engineering, culture, expansion, and transplantation, Cell processing, storage, and banking for therapeutic application, Preclinical and QC/QA assay development, Translational and clinical scale-up and Good Manufacturing procedures and process development, Clinical protocol development, Computational and bioinformatic methods for analysis, modeling, or visualization of biological data, Negotiating the regulatory approval process and obtaining such approval for clinical trials.
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