Author:
Legere Rebecca M.,Cohen Noah D.,Poveda Cristina,Bray Jocelyne M.,Barhoumi Rola,Szule Joseph A.,de la Concha-Bermejillo Andrés,Bordin Angela I.,Pollet Jeroen
Abstract
AbstractVaccines and therapeutics using in vitro transcribed mRNA hold enormous potential for human and veterinary medicine. Transfection agents are widely considered to be necessary to protect mRNA and enhance transfection, but they add expense and raise concerns regarding quality control and safety. We found that such complex mRNA delivery systems can be avoided when transfecting epithelial cells by aerosolizing the mRNA into micron-sized droplets. In an equine in vivo model, we demonstrated that the translation of mRNA into a functional protein did not depend on the addition of a polyethylenimine (PEI)-derived transfection agent. We were able to safely and effectively transfect the bronchial epithelium of foals using naked mRNA (i.e., mRNA formulated in a sodium citrate buffer without a delivery vehicle). Endoscopic examination of the bronchial tree and histology of mucosal biopsies indicated no gross or microscopic adverse effects of the transfection. Our data suggest that mRNA administered by an atomization device eliminates the need for chemical transfection agents, which can reduce the cost and the safety risks of delivering mRNA to the respiratory tract of animals and humans.
Funder
Department of Large Animal Clinical Sciences, Texas A
Grayson-Jockey Club Research Foundation
Link Equine Research Endowment, Texas A
Publisher
Springer Science and Business Media LLC
Cited by
12 articles.
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