Self-rearranging DNA vectors

Abstract

Disclosed are replicatable viral DNA vectors encoding a site-specific DNA-altering enzyme and a DNA target recognized by the enzyme, the enzyme selectively converting, in a cell expressing the enzyme, the DNA vector to a rearranged form. The invention further relates to methods for assembling recombinant adenoviral DNAs. These methods include the steps of: (a) providing a first linearized DNA vector including a restriction site and a cos site and a second linearized DNA vector including the restriction site, an adenoviral nucleic acid molecule, and a cos site; and (b) ligating the first and second linearized DNA vectors, the ligation assembling a recombinant adenoviral DNA.

Description

CROSS REFERENCE TO RELATED APPLICATIONS [0001] This application is divisional of U.S. application Ser. No. 10 / 384,136, filed Mar. 7, 2003, which is a continuation of International Application No. PCT / US01 / 27682, filed Sep. 7, 2001, which claims benefit of U.S. provisional application Nos. 60 / 246,904, and 60 / 231,053, filed Nov. 8, 2000, and Sep. 8, 2000, respectively, all of which are hereby incorporated by reference in their entirety.BACKGROUND OF THE INVENTION [0002] The invention relates to DNA vectors. [0003] Mammalian cell expression vectors based on DNA viruses have been widely discussed as gene delivery vehicles for genetic therapy. Among the different DNA viruses proposed for this purpose have been adenoviruses, baculovirus, Epstein Barr virus, and herpes simplex virus. In addition other smaller viruses that have an intranuclear phase in which the viral genome is present as a double stranded DNA, such as retroviruses and parvoviruses, have been proposed as gene delivery vehic...

AI Technical Summary

Benefits of technology

[0034] The presently claimed invention affords a number of advantages. For example, applicants' gene therapy vehicles, particularly those based on recombinant adenoviruses, minimize the propensity of the vectors to activate host immune surveillance, and thereby maximize the persistence for the DNA transduced. The invention therefore facilitates the development of gene delivery vectors designed to enhance persistence of virally delivered genes and evade the cellular immune response by severing the connection between the sole adenoviral enhancer and the sequences encoding potentially antigenic viral proteins.

[0039] For example, the circularization of an adenoviral vector via the action of Cre recombinase beneficially places a gene of interest (for example, a therapeutic gene) on a self-replicating episome. Vector circularization occurs in a tissue-targeted manner, for example, as a result of the activation of a synthetic liver-specific promoter upstream of the recombinase Cre. Once circularized, the EBV replicon in the episome confers improved persistence on the therapeutic gene as detected by reporter gene expression and direct assay for the presence of vector DNA sequences.

[0040] Furthermore, the invention eliminates the requirement for a helper virus, thus avoiding two potential limitations of that system. First, the continuous expression of Cre recombinase may lead to toxicity in host cells, either as a direct consequence of the protein's activity or via its immunogenicity. Second, the Cre helper virus may itself produce antigenic viral proteins that contribute to the immunologic elimination of infected host cells. In contrast, the self-resolving adenovirus / EBV vector system disclosed herein advantageously provides no alternative source of viral proteins, and Cre expression is terminated upon rearrangement.

[0042] The invention also provides a convenient general system for creating recombinant adenoviruses, which increase their attractiveness as gene transduction tools for basic research. The system, for example, employs two conventional plasmid vectors and a λ phage packaging step. The entire recombinant AdV genome is assembled into a single cosmid that is easily amplified in E. coli. The use of intron endonuclease recognition sequences flanking the ITRs enhances virus production while simplifying insertion of therapeutic gene sequences into the pLEP shuttle plasmid. The convenience of this vector system has facilitated the construction of over two hundred recombinant viruses to date.

Problems solved by technology

However to deploy these viruses on the scale required for human clinical application presents major challenges because a cesium chloride (CsCl) gradient is needed to remove the helper virus.

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