Novel Discrete Immolative Guanidinium Transporters Deliver mRNA Selectively to the Spleen, Lungs, and Red Blood Cells, Reaching the Brain

RNA-based therapeutics hold the potential to transform the prevention and treatment of disease with applications to therapeutic and prophylactic vaccinations, protein therapy, gene editing, cancer immunotherapy, and regenerative medicine. However, current systems used to deliver messenger RNA (mRNA), including those used in the COVID-19 vaccines, suffer from laborious syntheses, limited organ selectivity, formulation complexity, and undesired inflammatory responses mediated by the existence of persistently charged lipids in the body. This inspired the generation of a novel mRNA delivery system termed Discrete Immolative Guanidinium Transporters (DIGITs). Unlike most ionizable (ammonium) delivery systems, DIGITs are based on cationic guanidinium moieties, which complex mRNA at acidic pH and undergo irreversible charge neutralization at physiological pH to release their cargos in cells, enabling efficient RNA release and leaving behind neutral byproducts. Systematic evaluation of structural variations and formulations via in vivo bioluminescence assays, following delivery of fluorescent mRNA, led to the discovery of DIGIT/mRNA complexes that selectively target and deliver mRNA to the lungs, immune cells in the spleen, and even immature red blood cells in peripheral blood that can reach the brain. DIGIT/mRNA delivery systems, thus, provide a unique and innovative opportunity to develop cancer immunotherapies, personalized cancer vaccines, in vivo CAR T-cell therapies, and blood disorder and Alzheimer’s therapeutics, among other applications. This is supported by the finding that DIGIT/mRNA complexes are well-tolerated, following intravenous delivery, supporting their future utility in a variety of biomedical applications, affecting hundreds of millions of people worldwide.

Publication Details

Journal
Stanford Digital Repository
Published
2025-05-02
DOI
https://doi.org/10.25740/jd931kj7152
Primary Topic
RNA Interference and Gene Delivery
Type
article
Field-Weighted Citation Impact
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article

Novel Discrete Immolative Guanidinium Transporters Deliver mRNA Selectively to the Spleen, Lungs, and Red Blood Cells, Reaching the Brain

Stanford Digital Repository
RNA Interference and Gene Delivery
article

Novel Discrete Immolative Guanidinium Transporters Deliver mRNA Selectively to the Spleen, Lungs, and Red Blood Cells, Reaching the Brain

article en

Abstract

RNA-based therapeutics hold the potential to transform the prevention and treatment of disease with applications to therapeutic and prophylactic vaccinations, protein therapy, gene editing, cancer immunotherapy, and regenerative medicine. However, current systems used to deliver messenger RNA (mRNA), including those used in the COVID-19 vaccines, suffer from laborious syntheses, limited organ selectivity, formulation complexity, and undesired inflammatory responses mediated by the existence of persistently charged lipids in the body. This inspired the generation of a novel mRNA delivery system termed Discrete Immolative Guanidinium Transporters (DIGITs). Unlike most ionizable (ammonium) delivery systems, DIGITs are based on cationic guanidinium moieties, which complex mRNA at acidic pH and undergo irreversible charge neutralization at physiological pH to release their cargos in cells, enabling efficient RNA release and leaving behind neutral byproducts. Systematic evaluation of structural variations and formulations via in vivo bioluminescence assays, following delivery of fluorescent mRNA, led to the discovery of DIGIT/mRNA complexes that selectively target and deliver mRNA to the lungs, immune cells in the spleen, and even immature red blood cells in peripheral blood that can reach the brain. DIGIT/mRNA delivery systems, thus, provide a unique and innovative opportunity to develop cancer immunotherapies, personalized cancer vaccines, in vivo CAR T-cell therapies, and blood disorder and Alzheimer’s therapeutics, among other applications. This is supported by the finding that DIGIT/mRNA complexes are well-tolerated, following intravenous delivery, supporting their future utility in a variety of biomedical applications, affecting hundreds of millions of people worldwide.

Stanford Digital Repository
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RNA Interference and Gene Delivery
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