4.5 Article

The therapeutic potential of intrabodies in neurologic disorders - Focus on Huntington and Parkinson diseases

Journal

BIODRUGS
Volume 20, Issue 6, Pages 327-333

Publisher

ADIS INT LTD
DOI: 10.2165/00063030-200620060-00002

Keywords

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Funding

  1. NINDS NIH HHS [R01 NS053912-02, R01 NS053912] Funding Source: Medline
  2. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS053912] Funding Source: NIH RePORTER

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Single-chain Fv and single-domain antibodies retain the binding specificity of full-length antibodies but they can be cloned, selected, engineered, and manipulated as genes. When expressed intracellularly in mammalian cells these intracellular antibodies, or intrabodies, have the potential to alter the folding, interactions, modifications, or subcellular localization of their targets. These reagents have previously beer developed as therapeutics against cancer and HIV. Since misfolded and accumulated intracellular proteins characterize several major neurodegenerative disorders, including Huntington disease (HD) and Parkinson disease, these disorders are prime candidates for intrabody therapy. In this article we review the extension of intrabody technology to the nervous system. Studies of HD have been used to develop the approach and anti-synclein strategies are in the early stages of development. Such neurodegenerative diseases are therefore poised for engineered antibody approaches, which can provide a pipeline of novel therapeutics and new drug discovery tools.

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