{"id":45412,"date":"2012-05-25T18:25:25","date_gmt":"2012-05-25T18:25:25","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/gene-therapy-can-correct-forms-of-severe-combined-immunodeficiency.php"},"modified":"2012-05-25T18:25:25","modified_gmt":"2012-05-25T18:25:25","slug":"gene-therapy-can-correct-forms-of-severe-combined-immunodeficiency","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/gene-therapy\/gene-therapy-can-correct-forms-of-severe-combined-immunodeficiency.php","title":{"rendered":"Gene therapy can correct forms of severe combined immunodeficiency"},"content":{"rendered":"<p><p>Public  release date: 24-May-2012  [ |   E-mail   |  Share    ]  <\/p>\n<p>    Contact: Sarah Jackson    <a href=\"mailto:press_releases@the-jci.org\">press_releases@the-jci.org<\/a>    Journal of    Clinical Investigation<\/p>\n<p>    Severe combined immunodeficiency is defect in the immune system    that results in a loss of the adaptive immune cells known as B    cells and T cells. Mutations in several different genes can    lead to the development of severe combined immunodeficiency,    including mutation of the adenosine deaminase (ADA) gene.    Traditional treatment options, such as enzyme replacement    therapy, are of limited efficacy, but bone marrow transplant    from a compatible donor leads to a better response. A recent    clinical trial indicated that gene therapy to insert the    correct ADA gene in the patient's own bone marrow cells can    also lead to a good response.  <\/p>\n<p>    However, patients were noted to have defects in B cell    tolerance, meaning that some B cells that react to antigens    from the body fail to be eliminated, leading to an autoimmune    response. Dr. Eric Meffre and colleages at Yale University in    New Haven, Connecticut and Alessandro Aiuti in Milan, Italy    joined together to better understand why patients developed B    cell tolerance problems. They found that loss of the ADA gene    directly contributes to B cell tolerance problems and that    these defects are mostly corrected after gene therapy. Their    results point to a previously unknown role for ADA in B cell    response and support the use of gene therapy as an effective    treatment option for ADA-deficient severe combined    immunodeficiency patients.  <\/p>\n<p>    ###  <\/p>\n<p>    TITLE:  <\/p>\n<p>    Defective B cell tolerance in adenosine deaminase deficiency is    corrected by gene therapy  <\/p>\n<p>    AUTHOR CONTACT:  <\/p>\n<p>    Eric Meffre    Yale University School of Medicine, New Haven, CT, USA    Phone: 1-203-737-4535; Fax: 1-203-785-7903; E-mail: <a href=\"mailto:eric.meffre@yale.edu\">eric.meffre@yale.edu<\/a>  <\/p>\n<p>    ACCOMPANYING COMMENTARY  <\/p>\n<\/p>\n<p>Here is the original post: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.eurekalert.org\/pub_releases\/2012-05\/joci-gtc052212.php\" title=\"Gene therapy can correct forms of severe combined immunodeficiency\">Gene therapy can correct forms of severe combined immunodeficiency<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Public release date: 24-May-2012 [ | E-mail | Share ] Contact: Sarah Jackson <a href=\"mailto:press_releases@the-jci.org\">press_releases@the-jci.org<\/a> Journal of Clinical Investigation Severe combined immunodeficiency is defect in the immune system that results in a loss of the adaptive immune cells known as B cells and T cells. Mutations in several different genes can lead to the development of severe combined immunodeficiency, including mutation of the adenosine deaminase (ADA) gene <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/gene-therapy\/gene-therapy-can-correct-forms-of-severe-combined-immunodeficiency.php\">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":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[24],"tags":[],"class_list":["post-45412","post","type-post","status-publish","format-standard","hentry","category-gene-therapy"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/45412"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=45412"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/45412\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=45412"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=45412"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=45412"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}