Faster-Acting, Longer-Lasting Gene Therapy for RP Shows Promise
Long before the launch of gene therapy studies that have restored vision for patients with Leber congenital amaurosis (LCA), Foundation-funded researchers were hard at work refining their gene delivery technologies for future therapies to treat a broad spectrum of retinal degenerative diseases. They recognized that for certain retinal conditions, they needed to develop gene delivery technologies that: 1) worked more quickly; 2) provided a more sustained effect; and 3) worked more efficiently and effectively in photoreceptors.Their proactive efforts are now paying off.
Ji-jing Pang, M.D., Ph.D., a key team member from the University of Florida, says that the team is planning to evaluate the treatment in a canine study. Getting good results in a large animal model study is a critical step in moving the treatment into a clinical trial.
The investigators used a newly developed adeno-associated virus serotype 8 (AAV8), a manmade therapeutic virus, for gene delivery — an approach that proved to be fast-acting, sustained, and effective. Previous attempts to treat this mouse model with AAV5 delivery were not as successful, because the retina degenerated before the treatment began to work.
“Serotype” is a term used to describe the structure of the adeno-associated virus. Different AAV structures have different therapeutic properties. AAV8 has shown to be particularly effective in delivering corrective genes to photoreceptors. In this study, the investigators made a special modification to the outer structure of the AAV8 to further enhance the strength and speed of the therapy.
“When it comes to gene therapies, one size does not fit all,” says Stephen Rose, Ph.D., chief research officer, Foundation Fighting Blindness. “We need to tailor the delivery mechanism to fit the targeted disease and the cells to be treated. AAV2 has worked well for treating LCA in animals and humans. A completely different type of virus, a lentivrus developed by Oxford Biomedica, is showing promise for Stargardt disease, Usher syndrome, and age-related macular degeneration. The Foundation is also investing in nanoparticle research which may be effective for delivering corrective genes to the retina.”
Oxford Biomedica, a gene therapy developer in the United Kingdom, has received regulatory approval to begin a Phase I clinical trial of lentiviral gene therapy for Stargardt disease. The company plans to start the trial in mid-2011 at Oregon Health and Science University (Portland, Oregon) and Centre Hospitalier Nationale D’Opthalmologie des Quinze-Vingts (Paris, France). Their Phase I clinical trial of lentiviral gene therapy for the wet form of Üstüme transparanımsı bi gömlek giydim ve annem bi şey demesin diye üstüme de hırka aldım sikiş izle O da annemler 2 aylık tatile gittiler , hadi biz başlayalım dedi. üzerime doğra yaklaştı arkam da da yatak varmış porno Mert bazen arkama geçip balon alma niyetiyle bana sürtünüyodu sex hikayeleri Burdan dışarı çıkmak istiyosan anahtarı olduğu yerden al. Gittim elimi attım kilodunun içine.Anahtar yoktu.Ve türk porno bugün evire çevire sikemezsem bu resimleri hem Fayıma gösteririm elime durmadan onun penisi geliyodu sikiş Eteğim yatınca açılmıştı zaten porno izle Ağzımı bez barçasıyla çok sıkı bağladı rokettube Penisine tükürdü ve benim amcığıma parmağını sokup sokup çıkardı. Kızlığımı bozdu sonra tükürdü erotik hikayeler İçine boşalayımmı ha sikiş izle Ben başımı olumsuz şekilde yalvarır gibi salladım porno Ama içime boşaldı hayvan. öpüşürken kulağına senin birazdan götünü parçalayacağım dedim ataköy escort Hayır hiç yapmadım vermem dedi bayan escort amını yalamaya başladım anal escort birden bire hızlanmaya başlayarak kadını oracıkta boşalana kadar siktim. age-related macular degeneration is underway at Johns Hopkins University Hospital (Baltimore, Maryland).
Applied Genetic Technologies Corporation AGTC, a gene therapy company in Central Florida, has a Phase I clinical trial of an AAV-based gene therapy underway for LCA, and is developing gene therapies for achromatopsia (day blindness) and retinoschisis.
Both Oxford’s and AGTC’s therapies were made possible by preclinical research funded by the Foundation.
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