کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6140402 1594251 2014 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
ReviewDNA cleavage enzymes for treatment of persistent viral infections: Recent advances and the pathway forward
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ویروس شناسی
پیش نمایش صفحه اول مقاله
ReviewDNA cleavage enzymes for treatment of persistent viral infections: Recent advances and the pathway forward
چکیده انگلیسی


- Recent in vitro and in vivo results for DNA cleavage enzymes targeting persistent viral infections.
- Analysis of the best animal models for testing enzymes for HBV, HSV, HIV and HPV.
- Challenges facing in vivo delivery of therapeutic enzymes for persistent viral infections.
- Safety issues to be addressed with proper animal studies.

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.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Virology - Volumes 454–455, April 2014, Pages 353-361
نویسندگان
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