UNSPECIFIED. (2002) RNA bacteriophage capsid-mediated drug delivery and epitope presentation. INTERVIROLOGY, 45 (4-6). pp. 371-380. ISSN 0300-5526

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Abstract

Objective: To use our knowledge of the three-dimensional structure and self-assembly mechanism of RNA bacteriophage capsids to develop novel virus-like particles (VLPs) for drug delivery and epitope presentation. Methods: Site-directed mutagenesis of a recombinant MS2 coat protein expression construct has been used to generate translational fusions encompassing short epitope sequences. These chimeric proteins still self-assemble in vivo into T= 3 shells with the foreign epitope in an accessible location. Covalent conjugation has also been used to generate RNA stem-loops attached to the toxin, ricin A chain, or to nucleotide-based drugs, that are still capable of stimulating self-assembly of the capsid in vitro. These packaged drugs can then be directed to specific cells in culture by further covalent decoration of the capsids with targeting molecules. Results: Chimeric VLPs are strongly immunogenic when carrying either B or T cell epitopes, the latter generating cytokine profiles consistent with memory responses. Immune responses to the underlying phage epitopes appear to be proportional to the area of the phage surface accessible. Phage shells effectively protect nucleic acid-based drugs and, for the toxin construct, make cell-specific delivery systems with LD50 values in culture sub-nanomolar. Conclusion: VLP technology has potential for therapeutic and prophylactic intervention in disease. Copyright (C) 2003 S. Karger AG, Basel.

Item Type:	Journal Article
Subjects:	Q Science > QR Microbiology > QR355 Virology
Journal or Publication Title:	INTERVIROLOGY
Publisher:	KARGER
ISSN:	0300-5526
Official Date:	July 2002
Volume:	45
Number:	4-6
Number of Pages:	10
Page Range:	pp. 371-380
Identification Number:	10.1159/000067930
Publication Status:	Published
URI:	http://wrap.warwick.ac.uk/id/eprint/10045

Data sourced from Thomson Reuters' Web of Knowledge

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