Combinatorial lipid-like materials for intracellular delivery of small RNAs that activate innate antiviral immune responses and adjuvant vaccines

RNA-based therapy is an exciting new realm of experimental medicine due to the diverse roles of RNA in the human body. RNA function depends on sequence, structure, and cellular location. Whereas cytosolic short-interfering RNA (siRNA) can be used to turn off genes through RNA interference (RNAi), it was observed that the same siRNA can also activate an innate immune response. Recognition of RNA by specialized immune cells occurs through pattern recognition receptors, which have evolved to respond to RNA viruses, such as the Toll-like receptors (TLR) 7 and 8 located in the endosome of dendritic cells. Tailoring the multiple functions of RNA for a desired clinical application will require novel systems for intracellular delivery. A library of structurally-related cationic lipid-like materials, termed "lipidoids", was developed to facilitate uptake of small RNAs, and the role of drug delivery in controlling RNA function was investigated. In an experimental animal model of RNA interference of influenza virus, treatment with a lipidoid-siRNA nanoparticle efficiently activated a type I interferon response in a sequence-dependent manner suppressing lung viral titer over 97%. Specific chemical modifications to the siRNA prevented TLR7/8 engagement and also prevented antiviral responses, confirming an RNAi-independent mechanism of antiviral activity. Recognizing the therapeutic potential of immunostimulatory RNA (isRNA), a novel in vitro high- throughput assay was developed to screen the lipidoid library for delivery of isRNA.

Department dc:contributor.department

Massachusetts Institute of Technology. Department of Materials Science and Engineering

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2008

Author dc:creator

• Nguyen, David-Huy Nhu

Advisor dc:contributor.advisor

• Robert S. Langer.

• Materials Science and Engineering.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/45951

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/45951