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HSV as a gene transfer vector for the nervous system

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Abstract

Gene therapy for diseases of the nervous system requires vectors capable of delivering the therapeutic gene into postmitotic cells in vivo. Herpes simplex virus type 1 is a neurotropic virus that naturally establishes latency in neurons of the peripheral nervous system. Replication defective HSV vectors have been developed; these are deleted for at least one essential immediate early regulatory gene, rendering the virus less cytotoxic, incapable of reactivation, but still capable of establishing latency. Foreign genes can be vigorously expressed from an HSV-based vector in a transient manner in brain and other tissues. Long-term but weak foreign gene expression may be achieved in the nervous system by exploiting the transcriptional control mechanisms of the natural viral latency active promoter. To meet the needs of specific applications, either highly active long-term or regulatable transgene expression will be needed, requiring further studies in order to design the appropriate latency-based promoter systems.

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  1. Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, E1240 Biomedical Science Tower, 15261, Pittsburgh, PA

    Joseph C. Glorioso, Mary Ann Bender, William F. Goins & Neal DeLuca

  2. Department of Neurology, University of Michigan Medical School, Ann Arbor, MI

    David J. Fink

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  1. Joseph C. Glorioso
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Glorioso, J.C., Bender, M.A., Goins, W.F. et al. HSV as a gene transfer vector for the nervous system. Mol Biotechnol 4, 87–99 (1995). https://doi.org/10.1007/BF02907473

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