Engineered cells as programmable mRNA delivery vehicles

IF 42.7
Felix Horns, Victoria Tobin, Michael B. Elowitz
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Abstract

Delivering mRNA to specific cell types remains challenging. Recent work opens the possibility of using synthetic RNA transfer pathways to engineer mRNA ‘delivery cells’. These cells could home to disease sites, locally produce and deliver mRNA to target cells, and thereby enable targeted editing, reprogramming or elimination of selected cells for therapeutic benefit.

Abstract Image

工程细胞作为可编程mRNA传递载体
将mRNA递送到特定的细胞类型仍然具有挑战性。最近的工作开启了使用合成RNA转移途径来设计mRNA“传递细胞”的可能性。这些细胞可以回到疾病部位,在局部产生mRNA并将其传递给靶细胞,从而实现靶向编辑、重编程或消除选定的细胞以获得治疗益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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