| Apr 10, 2024 |
A new coating method in mRNA engineering points the way to advanced therapies
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(Nanowerk News) Medicine can help to treat certain illnesses, e.g., antibiotics can help overcome infections, but a new, promising field of medicine involves providing our body with the “blueprint” for how to defeat illnesses on its own.
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mRNA therapeutics is the delivery of messenger RNA (mRNA) molecules into the body, which the cellular machinery can use to make specific proteins. The field is rapidly advancing, especially because mRNA vaccines proved successful against COVID-19. However, the delivery of these engineered mRNAs to a specific organ has proved challenging.
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Now, a team at Tokyo Medical and Dental University (TMDU) has shown that coating the engineered mRNAs with a molecule called polyethylene glycol, or PEG, allows their delivery selectively to the spleen.
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The research has been published in Small Science ("Poly(ethylene Glycol) (PEG)–OligoRNA Hybridization to mRNA Enables Fine-Tuned Polyplex PEGylation for Spleen-Targeted mRNA Delivery").
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| Polymeric mRNA delivery nanoparticles. (a) Preparation scheme. (b) Behavior in the blood circulation. (Image: Department of Advanced Nanomedical Engineering, TMDU)
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To understand this achievement, let’s first discuss how mRNA therapeutics has worked until now. Engineered mRNAs have been packaged into structures called “polyplexes” for delivery into the body. The polyplex structures allow mRNAs to remain stable while outside cells and to be released in a controlled manner once inside cells. Once inside, the mRNAs are used by cellular machinery to produce proteins that are naturally dysfunctional or absent.
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Without modification, the polyplexes tend to accumulate in the lungs, as after injection into the blood they rapidly stick to each other and surrounding proteins and cells and become lodged in the lung’s blood vessels. Treating polyplexes with PEG, a process called “PEGylation”, prevents them from sticking together; however, applying PEG in a controlled, consistent manner to the polyplex surface is very difficult.
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The team at TMDU has developed a new method of PEGylation, where the mRNAs are hybridized to PEG molecules before the polyplexes are formed. Using this method, almost all the PEG strands mixed into the reaction become bound to the polyplexes, allowing much greater control over the final amount of PEG on the polyplex surface.
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Using a mouse model, the team found that the quantities and lengths of the PEG molecules significantly affected how well the mRNA therapy worked. A small number of short PEG molecules prevented accumulation of the engineered mRNAs in the lungs, facilitating effective delivery to the spleen. This approach has demonstrated utility in mRNA vaccines.
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“Our novel method allows fine tuning of the amount of PEGylation of mRNA polyplexes,” explains senior author Dr. Satoshi Uchida, “which in turn allows control of the physicochemical properties of the polyplexes, and thus their biological functionalities.”
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mRNA technology has wide-ranging potential for treating many diseases that have previously been considered incurable, as well as for the development of novel cancer treatments and vaccines. The development of this innovative technique paves the way for significant advances in the therapeutic use of mRNA polyplexes, with far-reaching potential consequences for human health.
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