Delivery strategies of RNA therapeutics to leukocytes
Harnessing RNA-based therapeutics for cancer, inflammation, and viral diseases is hindered by poor delivery of therapeutic RNA molecules. Targeting leukocytes to treat these conditions holds great promise, as they are key participants in their initiation, drug response, and treatment. The various ex...
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Published in | Journal of controlled release Vol. 342; pp. 362 - 371 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.02.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Harnessing RNA-based therapeutics for cancer, inflammation, and viral diseases is hindered by poor delivery of therapeutic RNA molecules. Targeting leukocytes to treat these conditions holds great promise, as they are key participants in their initiation, drug response, and treatment. The various extra- and intra-cellular obstacles that impediment the clinical implementation of therapeutic RNA can be overcome by utilizing drug delivery systems. However, delivery of therapeutic RNA to leukocytes poses an even greater challenge as these cells are difficult to reach and transfect upon systemic administration. This review briefly describes the existing successful delivery strategies that efficiently target leukocytes in vivo and discuss their potential clinical applicability.
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•RNA-based therapeutics can target proteins that are considered as "undruggable".•Clinically applying therapeutic RNA to leukocytes remains a significant hurdle.•Various nanocarriers demonstrated efficient delivery of therapeutic RNA in vivo.•Improving delivery systems is crucial to drive more FDA approvals of therapeutic RNA. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 0168-3659 1873-4995 |
DOI: | 10.1016/j.jconrel.2022.01.016 |