{"id":113989,"date":"2014-03-06T03:44:11","date_gmt":"2014-03-06T08:44:11","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/gene-therapy-shows-promise-for-hiv-control-without-drugs-study-eastday.php"},"modified":"2014-03-06T03:44:11","modified_gmt":"2014-03-06T08:44:11","slug":"gene-therapy-shows-promise-for-hiv-control-without-drugs-study-eastday","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/gene-therapy\/gene-therapy-shows-promise-for-hiv-control-without-drugs-study-eastday.php","title":{"rendered":"Gene therapy shows promise for HIV control without drugs: study-Eastday"},"content":{"rendered":"<p><p>    WASHINGTON, March 5 -- U.S. researchers said Wednesday they    have used gene therapy involving genetically engineered T-    cells to successfully decrease the amount of the AIDS virus in    several patients taken off antiretroviral drug therapy (ADT)    entirely, including one patient whose levels became    undetectable.  <\/p>\n<p>    The study, published in the U.S. journal New England Journal of    Medicine, is the first published report of any gene editing    approach in humans, the researchers said.  <\/p>\n<p>    \"This study shows that we can safely and effectively engineer    an HIV patient's own T cells to mimic a naturally occurring    resistance to the virus, infuse those engineered cells, have    them persist in the body, and potentially keep viral loads at    bay without the use of drugs,\" senior author Carl June,    professor of the University of Pennsylvania, said in a    statement.  <\/p>\n<p>    \"This reinforces our belief that modified T cells are the key    that could eliminate the need for lifelong ADT and potentially    lead to functionally curative approaches for HIV\/AIDS,\" June    said.  <\/p>\n<p>    In their study, the researchers used a technology called the    zinc finger nuclease (ZFN) to modify the T cells in 12 patients    with the AIDS virus in order to mimic the CCR5-delta-32    mutation that can provide a natural HIV resistance. Only one    percent of the general population carries that rare mutation.  <\/p>\n<p>    They then infused the modified cells known as SB-728-T into two    groups of patients, all treated with single infusions of about    10 billion cells, between May 2009 and July 2012.  <\/p>\n<p>    Six were taken off antiretroviral therapy altogether for up to    12 weeks, beginning four weeks after infusion, while six    patients remained on treatment.  <\/p>\n<p>    The researchers found that the amount of HIV dropped in four    patients whose treatment was interrupted for 12 weeks.  <\/p>\n<p>    One of those patients' viral loads dropped below the limit of    detection before reinstitution of ADT and the patient was later    found to be \"heterozygous\" for the CCR5-delta-32 gene mutation,    they said.  <\/p>\n<p>    \"This case gives us a better understanding of the mutation and    the body's response to the therapy, opening up another door for    study,\" co-author Bruce Levine, associate professor of the    University of Pennsylvania said.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Go here to see the original:<\/p>\n<p><a target=\"_blank\" href=\"http:\/\/english.eastday.com\/e\/140306\/u1a7963707.html\/RK=0\/RS=xBZEKTfGEt6N9Y0GUfdUMdlVt28-\" title=\"Gene therapy shows promise for HIV control without drugs: study-Eastday\">Gene therapy shows promise for HIV control without drugs: study-Eastday<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> WASHINGTON, March 5 -- U.S. researchers said Wednesday they have used gene therapy involving genetically engineered T- cells to successfully decrease the amount of the AIDS virus in several patients taken off antiretroviral drug therapy (ADT) entirely, including one patient whose levels became undetectable. The study, published in the U.S <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/gene-therapy\/gene-therapy-shows-promise-for-hiv-control-without-drugs-study-eastday.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-113989","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\/113989"}],"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=113989"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/113989\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=113989"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=113989"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=113989"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}