Golombek Sonia, Pilz Martin, Steinle Heidrun, Kochba Efrat, Levin Yotam, Lunter Dominique, Schlensak Christian, Wendel Hans Peter, Avci-Adali Meltem
Department of Thoracic and Cardiovascular Surgery, University Hospital Tübingen, Calwerstraße 7/1, 72076 Tübingen, Germany.
NanoPass Technologies Ltd., 3 Golda Meir, 7403648 Nes Ziona, Israel.
Mol Ther Nucleic Acids. 2018 Jun 1;11:382-392. doi: 10.1016/j.omtn.2018.03.005. Epub 2018 Mar 14.
In recent years, synthetic mRNA-based applications to produce desired exogenous proteins in cells have been gaining importance. However, systemic delivery of synthetic mRNA can result in unspecific uptake into undesired cells or organs and, thereby, fail to target desired cells. Thus, local and targeted delivery of synthetic mRNA becomes increasingly important to reach the desired cell types and tissues. In this study, intradermal delivery of synthetic mRNA using a hollow microneedle injection-based method was evaluated. Furthermore, an ex vivo porcine skin model was established to analyze synthetic mRNA-mediated protein expression in the skin following intradermal delivery. Using this model, highly efficient delivery of synthetic mRNA was demonstrated, which resulted in detection of high levels of secretable humanized Gaussia luciferase (hGLuc) protein encoded by the microinjected synthetic mRNA. Interestingly, synthetic mRNA injected without transfection reagent was also able to enter the cells and resulted in protein expression. The established ex vivo porcine skin model can be used to evaluate the successful production of desired proteins after intradermal delivery of synthetic mRNAs before starting with in vivo experiments. Furthermore, the use of microneedles enables patient-friendly, painless, and efficient delivery of synthetic mRNAs into the dermis; thus, this method could be applied for local treatment of different skin diseases as well as for vaccination and immunotherapy.
近年来,基于合成mRNA在细胞中产生所需外源蛋白的应用越来越重要。然而,合成mRNA的全身递送可能导致非特异性摄取到不需要的细胞或器官中,从而无法靶向所需细胞。因此,合成mRNA的局部和靶向递送对于到达所需的细胞类型和组织变得越来越重要。在本研究中,评估了使用基于中空微针注射的方法进行合成mRNA的皮内递送。此外,建立了一种离体猪皮肤模型,以分析皮内递送后皮肤中合成mRNA介导的蛋白表达。使用该模型,证明了合成mRNA的高效递送,这导致检测到由微注射的合成mRNA编码的高水平可分泌人源化高斯荧光素酶(hGLuc)蛋白。有趣的是,未使用转染试剂注射的合成mRNA也能够进入细胞并导致蛋白表达。所建立的离体猪皮肤模型可用于在开始体内实验之前评估皮内递送合成mRNA后所需蛋白的成功产生。此外,微针的使用能够以患者友好、无痛且高效的方式将合成mRNA递送至真皮;因此,该方法可应用于不同皮肤疾病的局部治疗以及疫苗接种和免疫治疗。