This AAV vector-based therapeutic treats inflammatory responses in mammals by delivering tissue-specific anti-inflammatory therapeutic proteins to targeted host cells. These transvected host cells then inhibit a variety of pro-inflammatory syndromes, which cause or exacerbate diseases and disorders caused by chronic inflammation. AAV vector-based gene therapy is useful in treating a number of diseases, including congestive heart failure, Parkinson’s disease, and hemophilia, by delivering therapeutics to targeted cells. Unfortunately, no available treatments combat tissue-specific inflammation, such as dry age-related macular degeneration. Age-related macular degeneration affects as many as 11 million people with global cost of visual impairment at $343 billion in the United States alone. University of Florida researchers have developed AAV vector constructs that are optimized for delivering anti-inflammatory peptides to selected mammalian cells and tissues. This tissue-specific treatment addresses symptoms of oxidative stress and inflammation by delivering secretable, cell-penetrating anti-inflammatory proteins to treat specific inflammatory diseases, such as dry age-related macular degeneration.
AAV vector-based therapy has been utilized in treating a number of genetic diseases; however, gene therapy has not traditionally been used to treat inflammatory diseases. This tissue-specific method of treating inflammation targets inflammatory responses by administering AAV vectors coupled with secretable, cell-penetrating anti-inflammatory proteins derived from viruses. These modified viral proteins penetrate target host cells; these suitably-transvected host cells then inhibit the key cellular inflammatory pathways that cause or exacerbate a variety of chronic progressive diseases, disorders, and conditions. Researchers have used this AAV vector-based therapy to treat dry age-related macular degeneration as an example of the therapy’s use in inhibiting pro-inflammatory responses in a number of mammalian diseases.
AAV vectors deliver modified viral protein as tissue-specific therapy for chronic inflammation
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congestive heart failure
cell-penetrating anti-inflammatory proteins
transvected host cells
suitably-transvected host cells
cell-penetrating viral therapeutics