{"id":400,"date":"2021-01-30T12:49:23","date_gmt":"2021-01-30T12:49:23","guid":{"rendered":"http:\/\/www.cscr.in\/nahd\/?page_id=400"},"modified":"2021-05-18T09:28:55","modified_gmt":"2021-05-18T09:28:55","slug":"late-pre-clinical-research-lentiviral","status":"publish","type":"page","link":"https:\/\/www.cscr.res.in\/nahd\/late-pre-clinical-research-lentiviral\/","title":{"rendered":"Gene Therapy for Thalassemia and Sickle Cell Disease:<br> Lentiviral Approach"},"content":{"rendered":"<div id=\"pl-400\"  class=\"panel-layout\" ><div id=\"pg-400-0\"  class=\"panel-grid panel-has-style\" ><div class=\"sp-small-para slide-icon-ss panel-row-style panel-row-style-for-400-0\" ><div id=\"pgc-400-0-0\"  class=\"panel-grid-cell\" ><div id=\"panel-400-0-0-0\" class=\"widget_text so-panel widget widget_custom_html panel-first-child panel-last-child\" data-index=\"0\" ><div class=\"textwidget custom-html-widget\"><div class=\"sp-new-noscroll\">\n\n<!--<div class=\"sp-title-cscr title-mbottom text-center\">\n<!--<h3 class=\"\"><u>PRECLINICAL MODEL FOR GENE THERAPY FOR THALASSEMIA AND SICKLE CELL DISEASE: Lentiviral<\/u><\/h3>-->\n<!--\t<h3 class=\"\"><u>Lentiviral Approach<\/u><\/h3>\n<\/div>-->\n\t\n\t\t\t<p class=\"text-justify\">Lentiviral vectors are the currently being used for gene therapy for several monogenetic diseases. We are developing novel lentiviral vectors for gene therapy for haemoglobinopathies. In collaboration with Dr. Trent Spencer, Emory University we developed two novel gene addition vectors, CSCREU1 and CSCREU2 to express beta globin and gamma globin genes. We have tested these two vectors in a sickle cell mouse model and were found to have significant expression of the transgenes resulting in phenotype correction. Additionally, we are in the process of developing a vector to express an shRNA for knocking down the expression of BCL11A for gene therapy for haemoglobinopathies. The initial studies performed in an ex-vivo erythropoiesis model showed that this vector can activate gamma globin gene significantly in the cultured erythroid cells. We are currently evaluating these vectors by transducing HSCs from patients with haemoglobinopathies with the generated lentiviruses and transplanting them in NSG\/NSGW mice.<\/p>\n\n<div class=\"sp-sec1-1\">\n\t<img src=\"http:\/\/www.cscr.res.in\/nahd\/jb-content\/uploads\/2021\/03\/1-Lentiviral.jpg\" alt=\"Lentiviral approach\" class=\"Lentiviral approach1 aligncenter\"><\/div>\t\t\t\t\t<br><br>\n<p style=\"margin-bottom: 0px;text-align:center;\">\t\t\t\n\t<span class=\"color-bold-1\">Figure:<\/span> Current approaches to gene theraphy for haemoglobin disorders\n<\/p>\n<br>\t\n\t\n<\/div>\n<\/div><\/div><\/div><\/div><\/div><div id=\"pg-400-1\"  class=\"panel-grid panel-no-style\" ><div id=\"pgc-400-1-0\"  class=\"panel-grid-cell panel-grid-cell-empty\" ><\/div><div id=\"pgc-400-1-1\"  class=\"panel-grid-cell panel-grid-cell-empty\" ><\/div><div id=\"pgc-400-1-2\"  class=\"panel-grid-cell\" ><div id=\"panel-400-1-2-0\" class=\"so-panel widget widget_sow-button panel-first-child panel-last-child\" data-index=\"1\" ><div class=\"so-widget-sow-button so-widget-sow-button-wire-d47fdd289bb7\"><div class=\"ow-button-base ow-button-align-center\">\n\t<a href=\"http:\/\/www.cscr.res.in\/nahd\/\" class=\"research-btn-aligntop ow-icon-placement-left ow-button-hover\" \t\t>\n\t\t<span>\n\t\t\t<span class=\"sow-icon-fontawesome sow-far\" data-sow-icon=\"&#xf0a5;\"\n\t\t ><\/span>\n\t\t\tBack to Home\t\t<\/span>\n\t<\/a>\n<\/div>\n<\/div><\/div><\/div><\/div><\/div>","protected":false},"excerpt":{"rendered":"<p>Lentiviral vectors are the currently being used for gene therapy for several monogenetic diseases. We are developing novel lentiviral vectors for gene therapy for haemoglobinopathies. In collaboration with Dr. Trent Spencer, Emory University we developed two novel gene addition vectors, CSCREU1 and CSCREU2 to express beta globin and gamma globin genes. We have tested these [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"pages\/right-sidebar-4.php","meta":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v16.3 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\r\n<title>Gene Therapy for Thalassemia and Sickle Cell Disease: Lentiviral Approach - CSCR NAHD<\/title>\r\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\r\n<link rel=\"canonical\" href=\"https:\/\/www.cscr.res.in\/nahd\/late-pre-clinical-research-lentiviral\/\" \/>\r\n<meta property=\"og:locale\" content=\"en_US\" \/>\r\n<meta property=\"og:type\" content=\"article\" \/>\r\n<meta property=\"og:title\" content=\"Gene Therapy for Thalassemia and Sickle Cell Disease: Lentiviral Approach - CSCR NAHD\" \/>\r\n<meta property=\"og:description\" content=\"Lentiviral vectors are the currently being used for gene therapy for several monogenetic diseases. We are developing novel lentiviral vectors for gene therapy for haemoglobinopathies. In collaboration with Dr. Trent Spencer, Emory University we developed two novel gene addition vectors, CSCREU1 and CSCREU2 to express beta globin and gamma globin genes. 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