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      DNA cleavage enzymes for treatment of persistent viral infections: recent advances and the pathway forward.

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          Abstract

          Treatment for most persistent viral infections consists of palliative drug options rather than curative approaches. This is often because long-lasting viral DNA in infected cells is not affected by current antivirals, providing a source for viral persistence and reactivation. Targeting latent viral DNA itself could therefore provide a basis for novel curative strategies. DNA cleavage enzymes can be used to induce targeted mutagenesis of specific genes, including those of exogenous viruses. Although initial in vitro and even in vivo studies have been carried out using DNA cleavage enzymes targeting various viruses, many questions still remain concerning the feasibility of these strategies as they transition into preclinical research. Here, we review the most recent findings on DNA cleavage enzymes for human viral infections, consider the most relevant animal models for several human viral infections, and address issues regarding safety and enzyme delivery. Results from well-designed in vivo studies will ideally provide answers to the most urgent remaining questions, and allow continued progress toward clinical application.

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          Author and article information

          Journal
          Virology
          Virology
          Elsevier BV
          1096-0341
          0042-6822
          Apr 2014
          : 454-455
          Affiliations
          [1 ] Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, E5-110, Seattle, WA 98109, USA; Department of Laboratory Medicine, University of Washington, Seattle, WA 98195, USA. Electronic address: nweber@fhcrc.org.
          [2 ] Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, E5-110, Seattle, WA 98109, USA. Electronic address: maubert@fhcrc.org.
          [3 ] Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, E5-110, Seattle, WA 98109, USA. Electronic address: cdang@fhcrc.org.
          [4 ] Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, E5-110, Seattle, WA 98109, USA. Electronic address: dstone2@fhcrc.org.
          [5 ] Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, E5-110, Seattle, WA 98109, USA; Department of Laboratory Medicine, University of Washington, Seattle, WA 98195, USA; Department of Microbiology, University of Washington, Seattle, WA 98195, USA. Electronic address: kjerome@fhcrc.org.
          Article
          S0042-6822(13)00709-5 NIHMS562607
          10.1016/j.virol.2013.12.037
          3988252
          24485787
          583a703c-ca94-4b29-ac03-6435f141b3b6
          History

          Targeted mutagenesis,DNA cleavage enzymes,Endonuclease,Gene therapy,Gene therapy delivery,Persistent viruses,Animal models

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