{"id":41316,"date":"2014-10-10T05:47:08","date_gmt":"2014-10-10T09:47:08","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/long-term-treatment-success-using-gene-therapy-to-correct-a-lethal-metabolic-disorder\/"},"modified":"2014-10-10T05:47:08","modified_gmt":"2014-10-10T09:47:08","slug":"long-term-treatment-success-using-gene-therapy-to-correct-a-lethal-metabolic-disorder","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genetic-engineering\/long-term-treatment-success-using-gene-therapy-to-correct-a-lethal-metabolic-disorder\/","title":{"rendered":"Long-term treatment success using gene therapy to correct a lethal metabolic disorder"},"content":{"rendered":"<p><p>    PUBLIC RELEASE DATE:  <\/p>\n<p>    9-Oct-2014  <\/p>\n<p>    Contact: Kathryn Ryan    <a href=\"mailto:kryan@liebertpub.com\">kryan@liebertpub.com<\/a>    914-740-2100    Mary Ann Liebert, Inc.\/Genetic    Engineering News    @LiebertOnline<\/p>\n<p>    New Rochelle, NY, October 9, 2014Excessive and often lethal    blood levels of bilirubin can result from mutations in a single    gene that are the cause of the metabolic disease known as    Crigler-Najjar syndrome type 1 (CNS1). A new gene therapy    approach to correcting this metabolic error achieved    significant, long-lasting reductions in bilirubin levels in a    mouse model of CNS1 and is described in an Open Access article    in Human Gene Therapy, a peer-reviewed journal from Mary    Ann Liebert, Inc., publishers. The article is available on the    Human Gene Therapy website at <a href=\"http:\/\/online.liebertpub.com\/doi\/full\/10.1089\/hum.2013.233\" rel=\"nofollow\">http:\/\/online.liebertpub.com\/doi\/full\/10.1089\/hum.2013.233<\/a>.  <\/p>\n<p>    In \"Life-Long    Correction of Hyperbilirubinemia with a Neonatal Liver-Specific    AAV-Mediated Gene Transfer in a Lethal Mouse Model of    CriglerNajjar Syndrome,\" Giulia Bortolussi and coauthors    from the International Centre for Genetic Engineering and    Biotechnology; Centro Studi Fegato, Fondazione Italiana Fegato;    and University of Trieste (Trieste, Italy) and Charles    University (Prague, Czech Republic), present details of the    adeno-associated virus (AAV)-mediated gene therapy approach    they used to correct the metabolic disorder that causes    hyperbilirubinemia in CNS1. The researchers reported 70-80%    reductions in plasma bilirubin levels early on among treated    animals, with about 50% reductions maintained throughout the    study. The authors compared the effectiveness of two delivery    strategies: targeting the therapeutic gene directly to the    liver or, preferably, to skeletal muscle. They discuss the    implications of the different results they obtained with each    approach.  <\/p>\n<p>    \"CNS1 is an outstanding model for in vivo gene therapy with    easily measured and clinically relevant metabolic endpoints,\"    says James M. Wilson, MD, PhD, Editor-in-Chief of Human Gene    Therapy, and Director of the Gene Therapy Program,    Department of Pathology and Laboratory Medicine, University of    Pennsylvania Perelman School of Medicine, Philadelphia.  <\/p>\n<p>    ###  <\/p>\n<p>    About the Journal  <\/p>\n<p>    Human Gene Therapy, the Official Journal of the European    Society of Gene and Cell Therapy, British Society for Gene and    Cell Therapy, French Society of Cell and Gene Therapy, German    Society of Gene Therapy, and five other gene therapy societies,    is an authoritative peer-reviewed journal published monthly in    print and online. Human Gene Therapy presents reports on    the transfer and expression of genes in mammals, including    humans. Related topics include improvements in vector    development, delivery systems, and animal models, particularly    in the areas of cancer, heart disease, viral disease, genetic    disease, and neurological disease, as well as ethical, legal,    and regulatory issues related to the gene transfer in humans.    Its sister journals, Human Gene Therapy Methods,    published bimonthly, focuses on the application of gene therapy    to product testing and development, and Human Gene    Therapy Clinical Development, published quarterly, features    data relevant to the regulatory review and commercial    development of cell and gene therapy products. Tables of    contents and sample issues for all three publications may be    viewed on the Human Gene Therapy website at <a href=\"http:\/\/www.liebertpub.com\/hgt\" rel=\"nofollow\">http:\/\/www.liebertpub.com\/hgt<\/a>.  <\/p>\n<p>    About the Publisher  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>See the article here:<br \/>\n<a target=\"_blank\" href=\"http:\/\/www.eurekalert.org\/pub_releases\/2014-10\/mali-lts100914.php\/RK=0\/RS=JWVX3fUzzRcQaVlOeBPQYVyBk2Q-\" title=\"Long-term treatment success using gene therapy to correct a lethal metabolic disorder\">Long-term treatment success using gene therapy to correct a lethal metabolic disorder<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> PUBLIC RELEASE DATE: 9-Oct-2014 Contact: Kathryn Ryan <a href=\"mailto:kryan@liebertpub.com\">kryan@liebertpub.com<\/a> 914-740-2100 Mary Ann Liebert, Inc.\/Genetic Engineering News @LiebertOnline New Rochelle, NY, October 9, 2014Excessive and often lethal blood levels of bilirubin can result from mutations in a single gene that are the cause of the metabolic disease known as Crigler-Najjar syndrome type 1 (CNS1). A new gene therapy approach to correcting this metabolic error achieved significant, long-lasting reductions in bilirubin levels in a mouse model of CNS1 and is described in an Open Access article in Human Gene Therapy, a peer-reviewed journal from Mary Ann Liebert, Inc., publishers. The article is available on the Human Gene Therapy website at <a href=\"http:\/\/online.liebertpub.com\/doi\/full\/10.1089\/hum.2013.233\" rel=\"nofollow\">http:\/\/online.liebertpub.com\/doi\/full\/10.1089\/hum.2013.233<\/a>.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/genetic-engineering\/long-term-treatment-success-using-gene-therapy-to-correct-a-lethal-metabolic-disorder\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[28],"tags":[],"class_list":["post-41316","post","type-post","status-publish","format-standard","hentry","category-genetic-engineering"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/41316"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=41316"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/41316\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=41316"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=41316"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=41316"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}