{"id":201997,"date":"2015-09-05T11:43:49","date_gmt":"2015-09-05T15:43:49","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/gene-therapy-for-diseases-asgct-american-society-of-gene.php"},"modified":"2015-09-05T11:43:49","modified_gmt":"2015-09-05T15:43:49","slug":"gene-therapy-for-diseases-asgct-american-society-of-gene","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/gene-therapy\/gene-therapy-for-diseases-asgct-american-society-of-gene.php","title":{"rendered":"Gene Therapy for Diseases | ASGCT &#8211; American Society of Gene &#8230;"},"content":{"rendered":"<p><p>Gene Therapy for Diseases    <\/p>\n<p>    Gene Therapy has made important medical advances in less than    two decades. Within this short time span, it has moved from the    conceptual stage to technology development and laboratory    research to clinical translational trials for a variety of    deadly diseases. Among the most notable advancements are the    following:  <\/p>\n<p>        Severe Combined Immune Deficiency (ADA-SCID)        ADA-SCID is also known as the bubble boy disease. Affected        children are born without an effective immune system and        will succumb to infections outside of the bubble without        bone marrow transplantation from matched donors. A landmark        study representing a first case of gene therapy \"cure,\" or        at least a long-term correction, for patients with deadly        genetic disorder was conducted by investigators in Italy.        The therapeutic gene called ADA was introduced into the        bone marrow cells of such patients in the laboratory,        followed by transplantation of the genetically corrected        cells back to the same patients. The immune system was        reconstituted in all six treated patients without        noticeable side effects, who now live normal lives with        their families without the need for further treatment.      <\/p>\n<p>        Chronic Granulomatus Disorder (CGD) CGD is a        genetic disease in the immune system that leads to the        patients' inability to fight off bacterial and fungal        infections that can be fatal. Using similar technologies as        in the ADA-SCID trial, investigators in Germany treated two        patients with this disease, whose reconstituted immune        systems have since been able to provide them with full        protection against microbial infections for at least two        years.      <\/p>\n<p>        Hemophilia Patients born with Hemophilia are not        able to induce blood clots and suffer from external and        internal bleeding that can be life threatening. In a        clinical trial conducted in the United States , the        therapeutic gene was introduced into the liver of patients,        who then acquired the ability to have normal blood clotting        time. The therapeutic effect however, was transient because        the genetically corrected liver cells were recognized as        foreign and rejected by the healthy immune system in the        patients. This is the same problem faced by patients after        organ transplantation, and curative outcome by gene therapy        might be achievable with immune-suppression or alternative        gene delivery strategies currently being tested in        preclinical animal models of this disease.      <\/p>\n<p>        Other genetic disorders After many years of        laboratory and preclinical research in appropriate animal        models of disease, a number of clinical trials will soon be        launched for various genetic disorders that include        congenital blindness, lysosomal storage disease and        muscular dystrophy, among others.      <\/p>\n<p>        Cancer Multiple gene therapy strategies have        been developed to treat a wide variety of cancers,        including suicide gene therapy, oncolytic virotherapy,        anti-angiogenesis and therapeutic gene vaccines. Two-thirds        of all gene therapy trials are for cancer and many of these        are entering the advanced stage, including a Phase III        trial of Ad.p53 for head and neck cancer and two different        Phase III gene vaccine trials for prostate cancer and        pancreas cancer. Additionally, numerous Phase I and Phase        II clinical trials for cancers in the brain, skin, liver,        colon, breast and kidney among others, are being conducted        in academic medical centers and biotechnology companies,        using novel technologies and therapeutics developed        on-site.      <\/p>\n<p>        Neurodegenerative Diseases Recent progress in        gene therapy has allowed for novel treatments of        neurodegenerative diseases such as Parkinson's Disease and        Huntington's Disease, for which exciting treatment results        have been obtained in appropriate animal models of the        corresponding human diseases. Phase I clinical trials for        these neurodegenerative disorders have been, or will soon        be, launched.      <\/p>\n<p>        Other acquired diseases The same gene        therapeutic techniques have been applied to treat other        acquired disorders such as viral infections (e.g.        influenza, HIV, hepatitis), heart disease and diabetes,        among others. Some of these have entered, or will soon be        entering, into early phase clinical trials.      <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>See the rest here: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.asgct.org\/about_gene_therapy\/diseases.php\" title=\"Gene Therapy for Diseases | ASGCT - American Society of Gene ...\">Gene Therapy for Diseases | ASGCT - American Society of Gene ...<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Gene Therapy for Diseases Gene Therapy has made important medical advances in less than two decades. Within this short time span, it has moved from the conceptual stage to technology development and laboratory research to clinical translational trials for a variety of deadly diseases.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/gene-therapy\/gene-therapy-for-diseases-asgct-american-society-of-gene.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-201997","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\/201997"}],"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=201997"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/201997\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=201997"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=201997"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=201997"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}