{"id":19412,"date":"2022-04-04T10:38:37","date_gmt":"2022-04-04T10:38:37","guid":{"rendered":"https:\/\/fundacionnoelia.org\/proyectos-de-investigacion\/optimizacion-de-vectores-virales-para-la-administracion-efectiva-de-terapias-genicas-a-celulas-del-musculo\/"},"modified":"2023-01-03T10:11:00","modified_gmt":"2023-01-03T10:11:00","slug":"optimization-of-viral-vectors-for-the-effective-gene-delivery-to-muscle-tissue-cells","status":"publish","type":"page","link":"https:\/\/fundacionnoelia.org\/en\/research-projects\/optimization-of-viral-vectors-for-the-effective-gene-delivery-to-muscle-tissue-cells\/","title":{"rendered":"Optimization of viral vectors for the effective gene delivery to muscle tissue cells"},"content":{"rendered":"[vc_row][vc_column width=&#8221;1\/6&#8243;][\/vc_column][vc_column width=&#8221;4\/6&#8243;][vc_empty_space]<figure class=\"vcex-image vcex-module wpex-clr textcenter\"><div class=\"vcex-image-inner wpex-relative wpex-inline-block\"><img decoding=\"async\" width=\"900\" height=\"601\" src=\"https:\/\/fundacionnoelia.org\/wp-content\/uploads\/2022\/03\/proyecto8.png\" class=\"wpex-align-middle\" alt=\"\" loading=\"lazy\" srcset=\"https:\/\/fundacionnoelia.org\/wp-content\/uploads\/2022\/03\/proyecto8.png 900w, https:\/\/fundacionnoelia.org\/wp-content\/uploads\/2022\/03\/proyecto8-300x200.png 300w, https:\/\/fundacionnoelia.org\/wp-content\/uploads\/2022\/03\/proyecto8-768x513.png 768w, https:\/\/fundacionnoelia.org\/wp-content\/uploads\/2022\/03\/proyecto8-600x401.png 600w\" sizes=\"auto, (max-width: 900px) 100vw, 900px\" \/><\/div><\/figure>[vc_empty_space][vc_column_text]\n<h2 class=\"icon_box_heading\">OPTIMIZATION OF VIRAL VECTORS FOR THE EFFECTIVE GENE DELIVERY TO MUSCLE TISSUE CELLS<\/h2>\n[\/vc_column_text][vc_empty_space][vc_column_text]Directed evolution of adeno-associated virus (AAV) capsids for effective gene delivery to the muscle fibro-adipogenic progenitors (FAPS)<\/p>\n<p><strong>PROJECT DESCRIPTION<\/strong><\/p>\n<p>In order to administer any gene therapy, it is necessary to make sure it effectively reaches the target cell. This is achieved by means of vectors that transport the therapy specifically to the cells we want to treat. Collagen VI-related muscular dystrophies (COL6-RD) are caused by mutations in one of the collagen VI genes, a protein produced by a specific type of cells present in the muscle (fibro-adipogenic progenitors). Today, although there are vectors used in the administration of gene therapies to certain cells, there is none that offers the efficiency or specificity necessary to reach this specific type of cell. The objective of this project is to design, based on currently available vectors, a new variant that allows any of the therapies being developed in other projects to be delivered efficiently to these cells, to restore the normal expression of collagen VI.<\/p>\n<p><strong>Project time frame<\/strong><\/p>\n<p>2021-2023<\/p>\n<p><strong>Funding<\/strong><\/p>\n<p>50.000,00 US Dollars, co-financed by Fundacion Noelia and Cure CMD.<\/p>\n<p><strong>Contributions made to date by Fundacion Noelia:<\/strong><br \/>\nDecember 1, 2021: <strong>12.500,00$\u00a0<\/strong> (<a href=\"https:\/\/fundacionnoelia.org\/wp-content\/uploads\/2022\/03\/Justificante-1a-transfer-dic21-1.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Proof of transfer<\/a>)<\/p>\n<p>December 1, 2021: <strong>12.500,00$\u00a0<\/strong> (<a href=\"https:\/\/fundacionnoelia.org\/wp-content\/uploads\/2023\/01\/2nd-proof-of-transfer-Project-AAV_FAPS_Dr-Bonneman.pdf\" target=\"_blank\" rel=\"noopener\">Proof of transfer<\/a>)<\/p>\n<p><strong>Location:<\/strong><br \/>\nNINDS National Institute of Neurological Disease and Stroke, Bethesda, Maryland EEUU<\/p>\n<p><strong>Researchers:<\/strong><\/p>\n<ul>\n<li>Carsten G. B\u00f6nnemann, MD (Principal Investigator)<\/li>\n<li>Veronique Bolduc (research fellow)<\/li>\n<li>Astrid Brull-Canagueral (postdoctoral fellow)<\/li>\n<li>Fady Guirguis (graduate student)<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><a href=\"https:\/\/fundacionnoelia.org\/wp-content\/uploads\/2022\/03\/2021-Grant-Agreement-Bonnemann-AAV-Fully-Executed-21-11-12-1.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Collaboration agreement.<\/a>[\/vc_column_text][\/vc_column][vc_column width=&#8221;1\/6&#8243;][\/vc_column][\/vc_row]\n","protected":false},"excerpt":{"rendered":"<p>[vc_row][vc_column width=&#8221;1\/6&#8243;][\/vc_column][vc_column width=&#8221;4\/6&#8243;][vc_empty_space][vc_empty_space][vc_column_text] OPTIMIZATION OF VIRAL VECTORS FOR THE EFFECTIVE GENE DELIVERY TO MUSCLE TISSUE CELLS [\/vc_column_text][vc_empty_space][vc_column_text]Directed evolution of adeno-associated virus (AAV) capsids for effective gene delivery to the muscle fibro-adipogenic progenitors (FAPS) PROJECT DESCRIPTION In order to administer any gene therapy, it is necessary to make sure it effectively reaches the target cell. This&hellip;<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":19389,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-19412","page","type-page","status-publish","hentry","entry","no-media"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Optimization of viral vectors for the effective gene delivery to muscle tissue cells - Fundaci\u00f3n Noelia<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/fundacionnoelia.org\/en\/research-projects\/optimization-of-viral-vectors-for-the-effective-gene-delivery-to-muscle-tissue-cells\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Optimization of viral vectors for the effective gene delivery to muscle tissue cells - Fundaci\u00f3n Noelia\" \/>\n<meta property=\"og:description\" content=\"[vc_row][vc_column width=&#8221;1\/6&#8243;][\/vc_column][vc_column width=&#8221;4\/6&#8243;][vc_empty_space][vc_empty_space][vc_column_text] OPTIMIZATION OF VIRAL VECTORS FOR THE EFFECTIVE GENE DELIVERY TO MUSCLE TISSUE CELLS [\/vc_column_text][vc_empty_space][vc_column_text]Directed evolution of adeno-associated virus (AAV) capsids for effective gene delivery to the muscle fibro-adipogenic progenitors (FAPS) PROJECT DESCRIPTION In order to administer any gene therapy, it is necessary to make sure it effectively reaches the target cell. 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