{"id":2856,"date":"2015-03-26T00:00:56","date_gmt":"2015-03-26T00:00:56","guid":{"rendered":"http:\/\/news.truthjuice.co.uk\/index.php\/get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s\/"},"modified":"2015-04-13T17:55:58","modified_gmt":"2015-04-13T17:55:58","slug":"get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s","status":"publish","type":"post","link":"https:\/\/news.truthjuice.co.uk\/index.php\/get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s\/","title":{"rendered":"Get Tomorrow\u2019s Anti-Aging Therapy \u2014 Available Today Outside the U.S."},"content":{"rendered":"<p><i><img decoding=\"async\" class=\"alignleft  wp-image-27293\" src=\"https:\/\/news.truthjuice.co.uk\/wp-content\/plugins\/wp-o-matic\/cache\/3808f54c56_bioviva.png\" alt=\"bioviva\" data-recalc-dims=\"1\" \/>For people who have a few hundred thousand dollars to spend and are willing to take on the risks of an \u201cearly adopter\u201d and travel to South America, options are now becoming available that were inconceivable just a few years ago. A new company is leapfrogging over the time-consuming process of testing and regulatory approval, and offering the best-established and most promising experimental anti-aging technologies in the near future. This is a new vision for combining research with treatment, for treating diseases that have no proven therapies, and for aging itself.<\/i><\/p>\n<p>(This column begins with a couple of pages of background. \u00a0If you want to cut to the chase, scroll down to <a href=\"http:\/\/joshmitteldorf.scienceblog.com\/2015\/03\/18\/tomorrows-anti-aging-therapy-available-today\/#Bioviva\">BioViva<\/a>.)<\/p>\n<hr \/>\n<p>You only have to read <a href=\"http:\/\/time.com\/3706701\/cure-for-aging\/\">Time Magazine<\/a> to notice that this is the year anti-aging medicine is coming of age. \u00a0Promising life extension technologies are being debuted, with potential for preventing many diseases at once, adding decades to the human life span, and restoring youthful function to an aging body. These include telomerase therapies, stem cell therapies, epigenetic reprogramming, removal of senescent cells, plasma transfer, and hormonal therapies inspired by gene expression changes between young and old.<\/p>\n<p>Inevitably, this has brought a surge in the number of companies eager to jump the gun and offer treatments to consumers based on early lab research, before the technology has proved \u00a0safe and effective in humans. \u00a0In an age of wildcat capitalism, we are well-advised to approach all claims with a skeptical eye, and assume that hucksterism is rampant. \u00a0Anyone who considers signing on with a new company that is offering a promising but unproven anti-aging technology had best start with a foundation of second opinions and broad considerations of risk and rewards.<\/p>\n<p>But I stop short of saying, \u201cstay away\u201d. \u00a0The field is too important, with too much at stake for us individually and as a human community, to sit on the sidelines, to wait for the research to be sorted out. \u00a0Political control of medical research has protected us imperfectly, and has held back life-saving treatments, sometimes for decades. \u00a0The system serves <a href=\"http:\/\/www.bbc.com\/news\/business-28212223\">pharmaceutical profits<\/a> more effectively than the public of medical consumers. \u00a0Too often, the treatments that are approved are not those that offer the best risk\/reward ratio, but those that are patentable and owned by someone who can afford to invest <a href=\"http:\/\/www.publicintegrity.org\/2005\/07\/07\/5786\/drug-lobby-second-none\">hundreds of millions of dollars in scientific advocacy<\/a>.<\/p>\n<p>The standard path to regulatory approval respects individual human life, and is \u201cconservative\u201d in the Hippocratic sense of \u201cfirst do no harm\u201d. \u00a0But it is far from the most effective way to move science forward, and probably is not the most efficient way to save the most lives, even in the short run. \u00a0Many libertarians, anti-aging enthusiasts and ordinary citizens who find themselves with a condition for which there is currently no effective medical treatment want the freedom to participate in experimental medicine, and experimental medicine certainly wants to try to help them and to learn from successes and failures.<\/p>\n<p>For people who see their options for an active and creative life being closed by age-related disabilities, for people who are willing to take personal risks to help move the science forward, for people who are bold and adventure-seeking, the choice to try experimental anti-aging technologies can be a rational decision.<\/p>\n<p><strong><strong>\u00a0<\/strong><\/strong><\/p>\n<p><b>The Promise of Telomerase Therapies<\/b><\/p>\n<p>In my opinion, the best-validated and most promising of the experimental therapies is the direct delivery of telomerase through gene therapy. \u00a0This is a technology pioneered in mice by <a href=\"http:\/\/www.cnio.es\/ES\/grupos\/plantillas\/curriculum.asp?pag=39\">Maria Blasco<\/a>\u2019s lab in Madrid, with stunning results. \u00a0In a <a href=\"http:\/\/embomolmed.embopress.org\/content\/4\/8\/691.abstract\">ground-breaking 2012 paper<\/a>by Blasco\u2019s student <a href=\"https:\/\/www.researchgate.net\/profile\/Bruno_Bernardes_de_Jesus\">Bruno Bernardes de Jesus<\/a>, ordinary lab mice were given gene therapy with an \u201cextra\u201d telomerase gene spread to their cells by a genetically-engineered virus. \u00a0the mice lived 13-24% longer, and the experimenters reported \u201cremarkable beneficial effects on health and fitness, including insulin sensitivity, osteoporosis, neuromuscular coordination and several molecular biomarkers of aging.\u201d<\/p>\n<p>Some strategies work better in mice than in humans, but there is theoretical reason to believe that this technique should work (even) better in humans than in mice. \u00a0Untreated mice already have plenty of telomerase, and the telomeres of lab mice are at least 3 times as long as humans\u2019, with shorter life spans in which to lose their telomeres. \u00a0Before the above experiment, it was reasonable to think that telomere length was a primary aging clock in humans, but not in mice. \u00a0Mice can <a href=\"http:\/\/jcb.rupress.org\/content\/139\/2\/309.short\">live up to six generations<\/a> after their telomerase gene has been knocked out (no telomerase at all), whereas people exhaust their telomere endowment in a single generation.<\/p>\n<p>I\u2019ve <a href=\"http:\/\/joshmitteldorf.scienceblog.com\/telomerase-as-a-fountain-of-youth\/\">written in the past<\/a> about telomere length as one of the body\u2019s primary aging clocks. \u00a0Very little telomerase is expressed in human adults. \u00a0As our stem cells divide during a lifetime, telomeres get progressively shorter with age. \u00a0Some results include the most important symptoms of aging:<\/p>\n<ul>\n<li>fewer functioning stem cells to replenish the stock of blood and skin cells<\/li>\n<li>more senescent cell, each sending out distress signals that promote the body\u2019s hyper-inflamed state<\/li>\n<li>decline of the immune system, as new white blood cells form more slowly<\/li>\n<li>a cascade effect, as cells with short telomeres senesce and then trigger senescence in neighboring cells<\/li>\n<li>higher cancer rates, as the chromosomes in cells with short telomeres become unstable, and the immune system sentinels that nip cancer in the bud go AWOL.<\/li>\n<\/ul>\n<p>Yes\u2014higher cancer rates result when telomeres get short. \u00a0There is a theory that our bodies withhold telomerase in order to prevent cancer, but it is an <a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/24228928\">idea with no experimental support<\/a>. \u00a0Fear of cancer has held back telomerase therapy, and this is a red herring, based on misunderstanding of evolutionary biology. \u00a0All evidence suggests that telomerase therapies will\u00a0<strong><em>lower cancer risk<\/em><\/strong>.<\/p>\n<p><strong><strong>\u00a0<\/strong><\/strong><\/p>\n<p><a><\/a><b>BioViva<\/b><\/p>\n<p><a href=\"http:\/\/www.bioviva-science.com\/\"><b>BioViva<\/b><\/a> is a new company offering experimental medical services outside US borders. \u00a0<a href=\"http:\/\/www.bioviva-science.com\/projects-1-1-1-1-1\/\">Their team<\/a> includes<\/p>\n<ul>\n<li>a lab that provides genetically modified viruses with a gene payload, made to order. \u00a0(This has now become a reliable and predictable technology.)<\/li>\n<li>A doctor who has experience with experimental gene therapy, and who had the courage to experiment on himself five years ago, with good outcome thus far.<\/li>\n<li>Sites in Colombia and Mexico where doctors will administer therapies for which there is not yet FDA approval.<\/li>\n<li>Most important, a Scientific Advisory Board that includes two of the most prominent, senior biochemists who developed the science of telomerase in the 1990s and before. \u00a0They are Bill Andrews and Michael Fossel.<\/li>\n<\/ul>\n<p>What they offer is gene therapy with hTERT and a proprietary myostatin inhibitor \u201cin the same family with GDF-11,\u201d according to CEO Elizabeth Parrish.<\/p>\n<p>Parrish stresses that AAV gene therapy is a mature technology and has already passed\u00a0FDA tests for safety. \u00a0\u201cAAV has become increasingly common as a vector for use in human clinical trials; as of [2008], 38 protocols have been approved by the Recombinant DNA Advisory Committee and the Food and Drug Administration (FDA).\u201d [<a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC2570152\/\" target=\"_blank\">ref<\/a>] The uncertainties are no longer about safety, but about whether the virus will be destroyed by the body\u2019s immune system before their payload can be delivered. \u00a0The rejuvenation benefit is likely to be systemic,\u00a0and will have ripple consequences that we can only learn with human subjects.<\/p>\n<p>In a surprise marketing move, Parrish has offered a guarantee for Patient #1 only. \u00a0If results for the first patient are disappointing, and Bioviva learns to avoid pitfallss and do a better job over the next 2 years, Patient #1 will be re-treated without cost, using the updated technology.<\/p>\n<p><strong><strong>\u00a0<\/strong><\/strong><\/p>\n<p><b>How Gene Therapy Works with AAV<\/b><\/p>\n<p>AAV stands for Adeno-Associated Viruses, and there are several types in use. \u00a0This virus makes its living by<\/p>\n<ul>\n<li>slipping its payload of DNA into a human cell (shedding its protein shell at the cell wall)<\/li>\n<li>finding its way to the cell nucleus<\/li>\n<li>copying itself into a specific place on Chromosome 19,<\/li>\n<li>from where it manufactures copies of its own DNA, and also of the proteins that it needs to replicate, to penetrate other cells.<\/li>\n<\/ul>\n<p>In therapeutic applications, the AAV DNA strand is modified to include a payload of therapeutic DNA, and to eliminate the genes coding for proteins that AAV needs in order to reproduce. \u00a0In this form, the modified virus can infect a cell, but once inside it cannot reproduce, infect more cells, reproduce there, and spread, causing disease. \u00a0It becomes a one-trick pony. \u00a0Each individual virus can infect one cell only, and then it has shot its wad. \u00a0No way this infection can \u201cgo viral\u201d.<\/p>\n<p>AAV therapy has been studied for <a href=\"http:\/\/www.pnas.org\/content\/87\/6\/2211.full.pdf+html?sid=b3e80d13-02c4-437f-95f7-a9032aaacb2a\">over 25 years<\/a>, and there is some reason to expect that the payload gene can remain active for a long time. \u00a0So this is a permanent change in the DNA of some cells in the body, though it is not a permanent infection. \u00a0Though AAVs are common in the environment, <a href=\"http:\/\/www.nature.com\/gt\/journal\/v10\/n11\/full\/3302039a.html\">80% of us have a naive immune response<\/a>, so the treatment can be effective. \u00a0(For the other 20%, temporary immune suppression may be necessary.) \u00a0Repeat treatments are sometimes possible. \u00a0<a href=\"http:\/\/www.genetherapynet.com\/viral-vector\/adeno-associated-viruses.html\">Here<\/a> is a good semi-technical introduction to the subject.<\/p>\n<blockquote>\n<p><a href=\"http:\/\/www.genetherapynet.com\/glossary-of-gene-therapy-terms.html#aav\">Adeno-associated viruses<\/a>, from the parvovirus family, are small viruses with a <a href=\"http:\/\/www.genetherapynet.com\/glossary-of-gene-therapy-terms.html#genome\">genome<\/a> of single stranded <a href=\"http:\/\/www.genetherapynet.com\/glossary-of-gene-therapy-terms.html#dna\">DNA<\/a>. These viruses can insert genetic material at a specific site on <a href=\"http:\/\/www.genetherapynet.com\/glossary-of-gene-therapy-terms.html#chromosomes\">chromosome<\/a> 19 with near 100% certainty. There are a few disadvantages to using AAV, including the small amount of DNA it can carry (low capacity) and the difficulty in producing it. This type of <a href=\"http:\/\/www.genetherapynet.com\/glossary-of-gene-therapy-terms.html#virus\">virus<\/a> is being used, however, because it is non-pathogenic (most people carry this harmless virus). In contrast to <a href=\"http:\/\/www.genetherapynet.com\/glossary-of-gene-therapy-terms.html#adenovirus\">adenoviruses<\/a>, most people treated with AAV will not build an immune response to remove the virus and the <a href=\"http:\/\/www.genetherapynet.com\/glossary-of-gene-therapy-terms.html#cell\">cells<\/a> that have been successfully treated with it.<\/p>\n<\/blockquote>\n<p>Different AAV viruses can be customized to infect different cell types, and of course the place where the virus is injected is the most likely place for the virus to take root. \u00a0Viruses used in previous generations of gene therapy tended to disrupt the body\u2019s own DNA by inserting at sites that are essential, and cancer rates were raised by some early forms of gene therapy. \u00a0AAV is favored because its target site seems to be safe, and its insertion harmless.<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p><b>Therapies with hTERT and Myostatin Inhibitor<\/b><\/p>\n<p>hTERT is only half the telomerase molecule, but it is the half that is in short supply, and hence the bottleneck for production of telomerase. \u00a0Of course, the DNA in our every cell contains the hTERT gene, but it is covered up and remains un-expressed almost all the time. \u00a0The new copy on Chromosome 19 is active, and in tests in cell cultures and live mice, telomeres have been lengthened.<\/p>\n<p>I believe that telomerase is the closest thing we have at present to a cure for aging. \u00a0<a href=\"http:\/\/sierrasci.com\/\">Bill Andrews<\/a> and others have a long-term goal of developing drugs that will signal the body to activate its own telomerase gene, but these seem to be a few years off. \u00a0For now, adding an extra gene for hTERT may be the most promising generalized anti-aging intervention. \u00a0An important issue is that a large viral dose may be needed to saturate the body\u2019s stem cells with the gene payload. \u00a0This is because a small minority of cells with the shortest telomeres is the source of some of the body\u2019s biggest problems. \u00a0We\u2019ll learn about the body\u2019s response\u2014if we are lucky, a rejuvenated immune system will itself eliminate the residual senescent cells without the need to lengthen telomeres in every senescent cell.<\/p>\n<p>The myostatin strategy grows from (of all things) body-enhancement strategies for muscle-builders. \u00a0Myostatin is a member of the <a href=\"http:\/\/joshmitteldorf.scienceblog.com\/2013\/11\/12\/molecules-in-the-blood-that-signal-self-destruction\/\">TGF-\u03b2 family<\/a>, is also called GDF-8*, and is a gene that inhibits muscle growth. \u00a0So if myostatin can be tied up, there is less inhibition and more muscle growth. \u00a0In the last several years, <a href=\"http:\/\/www.muscleandbodymag.com\/creatine-myostatins-enemy\/\">creatine<\/a> has become a popular supplement for body-builders, and it works directly at the level of the gene, by inhibiting expression of myostatin=GDF-8. \u00a0Later in life, expression of the <a href=\"http:\/\/eurekaselect.com\/87158\">myostatin gene increases<\/a>, and it is thought, logically enough, that this is a cause of the loss of muscle mass (sarcopoenia) that is almost universal with aging (though it is <a href=\"http:\/\/scholar.google.com\/scholar_url?url=http:\/\/www.researchgate.net\/profile\/Stephen_Roth2\/publication\/10736474_Myostatin_gene_expression_is_reduced_in_humans_with_heavy-resistance_strength_training_a_brief_communication\/links\/0046352972a7b2603a000000.pdf&amp;hl=en&amp;sa=X&amp;scisig=AAGBfm1aVg_jjzMBBV63Um3UDJ7NOWy5qQ&amp;nossl=1&amp;oi=scholarr\">mitigated by exercise<\/a>). \u00a0Bioviva offers gene therapy for a myostatin inhibitor (the specific gene is not disclosed), and it has been tried by one of the team members, experimenting on himself 5 years ago, with good results in a<i>younger man<\/i>. \u00a0<a href=\"http:\/\/www.researchgate.net\/profile\/Nathan_LeBrasseur\/publication\/259882218_Myostatin_and_Sarcopenia_Opportunities_and_Challenges_-_A_Mini-Review\/links\/545105d30cf249aa53dc8f81.pdf\">Here<\/a> is an article that offers a balanced view of reasons to believe this might or might not work for age-related sarcopoenia.<\/p>\n<p>Perhaps more important, the same gene has been found to clear blocked arteries, with expected reduction of the risk for heart disease and stroke. \u00a0There is <a href=\"http:\/\/diabetes.diabetesjournals.org\/content\/58\/8\/1739.short\">rodent data<\/a> and good <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0009898114001296\">theoretical reason<\/a> to expect this will work, and there has been one heart patient who has received the AAV\/myostatin treatment it with excellent results. \u00a0Blocking myostatin is also expected to <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0009898114001296\">reduce the progression of insulin resistance<\/a> that is a driver of many age-related diseases.<\/p>\n<p><strong><strong>\u00a0<\/strong><\/strong><\/p>\n<p><b>Alzheimer\u2019s Disease<\/b><\/p>\n<p>There is a well-supported theory of AD that it has its roots in the microglial cells of the brain. \u00a0These are not nerve cells, but they act as a kind of immune system for the brain, protecting it from inflammation and cleaning up plaques. \u00a0Their secretions promote growth and repair. \u00a0Unlike nerve cells, microglia are continually replicating, and so they <a href=\"http:\/\/online.liebertpub.com\/doi\/abs\/10.1089\/rej.2006.9096\">lose telomere length over time<\/a>. \u00a0On the theory that restoring telomeres in the microglia will reverse dementia, Bioviva is offering gene therapy with hTERT in the brain as treatment for AD. \u00a0Direct evidence that this might work comes from a <a href=\"http:\/\/www.nature.com\/nature\/journal\/v469\/n7328\/full\/nature09603.html\">2011 experiment<\/a> from the de Pinho lab at Harvard Med School, in which brains atrophied in mice deprived of telomerase, and the brains actually regrew when telomerase was provided.<\/p>\n<p><strong><strong>\u00a0<\/strong><\/strong><\/p>\n<p><b>The Bottom Line<\/b><\/p>\n<p>Experimental treatments are, by definition, at the wrong end of the learning curve. \u00a0But there is so much to be gained, and the people involved are such experts, that I am deeply hopeful about Bioviva\u2019s work, and the prospect of a fast track to meaningful anti-aging therapies.<\/p>\n<p>____________________<\/p>\n<p>* Myostatin is GDF-8, not to be confused with GDF-11, which has also been recently in the news. \u00a0Both are in the TGF-\u00df family. \u00a0GDF-8 inhibits <b><i>muscle <\/i><\/b>cell growth, while GDF-11 inhibits<b><i> nerve<\/i><\/b> cell growth. \u00a0Curiously, Bioviva\u2019s anti-aging strategy is to <b><i>suppress GDF-8<\/i><\/b>but <a href=\"http:\/\/www.sciencemag.org\/content\/344\/6184\/649\">last year\u2019s headline-making paper<\/a> from Harvard found benefits in \u00a0<b><i>promoting GDF-11<\/i><\/b>.<\/p>\n<p>###<\/p>\n<p>This article originally appeared in Josh&#8217;s Aging Matters blog <a href=\"http:\/\/joshmitteldorf.scienceblog.com\/2015\/03\/18\/tomorrows-anti-aging-therapy-available-today\/\" target=\"_blank\">here<\/a>. Republished with permission of the author.<\/p>\n<p>The post <a rel=\"nofollow\" href=\"http:\/\/hplusmagazine.com\/2015\/03\/26\/get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s\/\">Get Tomorrow\u2019s Anti-Aging Therapy &#8212; Available Today Outside the U.S.<\/a> appeared first on <a rel=\"nofollow\" href=\"http:\/\/hplusmagazine.com\">h+ Media<\/a>.<\/p>\n<!-- AddThis Advanced Settings generic via filter on the_content --><!-- AddThis Share Buttons generic via filter on the_content --><!-- AddThis Related Posts generic via filter on the_content -->","protected":false},"excerpt":{"rendered":"<p>For people who have a few hundred thousand dollars to spend and are willing to take on the risks of an \u201cearly adopter\u201d and travel to South America, options are now becoming available that were inconceivable just a few years ago. A new company is leapfrogging over the time-consuming process of testing and regulatory approval, &hellip; <\/p>\n<p><a class=\"more-link block-button\" href=\"https:\/\/news.truthjuice.co.uk\/index.php\/get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s\/\">Continue reading &raquo;<\/a><!-- AddThis Advanced Settings generic via filter on wp_trim_excerpt --><!-- AddThis Share Buttons generic via filter on wp_trim_excerpt --><!-- AddThis Related Posts generic via filter on wp_trim_excerpt --><\/p>\n","protected":false},"author":7,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[78,69],"tags":[],"class_list":["post-2856","post","type-post","status-publish","format-standard","hentry","category-tj-archive","category-transhumanism","nodate"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v19.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Get Tomorrow\u2019s Anti-Aging Therapy \u2014 Available Today Outside the U.S. - TruthJuice News<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/news.truthjuice.co.uk\/index.php\/get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s\/\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Get Tomorrow\u2019s Anti-Aging Therapy \u2014 Available Today Outside the U.S. - TruthJuice News\" \/>\n<meta property=\"og:description\" content=\"For people who have a few hundred thousand dollars to spend and are willing to take on the risks of an \u201cearly adopter\u201d and travel to South America, options are now becoming available that were inconceivable just a few years ago. 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A new company is leapfrogging over the time-consuming process of testing and regulatory approval, &hellip; Continue reading &raquo;","og_url":"https:\/\/news.truthjuice.co.uk\/index.php\/get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s\/","og_site_name":"TruthJuice News","article_published_time":"2015-03-26T00:00:56+00:00","article_modified_time":"2015-04-13T17:55:58+00:00","og_image":[{"url":"http:\/\/news.truthjuice.co.uk\/wp-content\/plugins\/wp-o-matic\/cache\/3808f54c56_bioviva.png"}],"author":"The Architect","twitter_misc":{"Written by":"The Architect","Estimated reading time":"12 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/news.truthjuice.co.uk\/index.php\/get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s\/","url":"https:\/\/news.truthjuice.co.uk\/index.php\/get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s\/","name":"Get Tomorrow\u2019s Anti-Aging Therapy \u2014 Available Today Outside the U.S. - TruthJuice News","isPartOf":{"@id":"https:\/\/news.truthjuice.co.uk\/#website"},"datePublished":"2015-03-26T00:00:56+00:00","dateModified":"2015-04-13T17:55:58+00:00","author":{"@id":"https:\/\/news.truthjuice.co.uk\/#\/schema\/person\/850fb4325758ef62e0feb0b6af06e039"},"breadcrumb":{"@id":"https:\/\/news.truthjuice.co.uk\/index.php\/get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s\/#breadcrumb"},"inLanguage":"en-GB","potentialAction":[{"@type":"ReadAction","target":["https:\/\/news.truthjuice.co.uk\/index.php\/get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/news.truthjuice.co.uk\/index.php\/get-tomorrows-anti-aging-therapy-available-today-outside-the-u-s\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/news.truthjuice.co.uk\/"},{"@type":"ListItem","position":2,"name":"Get Tomorrow\u2019s Anti-Aging Therapy \u2014 Available Today Outside the U.S."}]},{"@type":"WebSite","@id":"https:\/\/news.truthjuice.co.uk\/#website","url":"https:\/\/news.truthjuice.co.uk\/","name":"TruthJuice News","description":"For the Truthseeker and Freethinker","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/news.truthjuice.co.uk\/?s={search_term_string}"},"query-input":"required name=search_term_string"}],"inLanguage":"en-GB"},{"@type":"Person","@id":"https:\/\/news.truthjuice.co.uk\/#\/schema\/person\/850fb4325758ef62e0feb0b6af06e039","name":"The Architect","image":{"@type":"ImageObject","inLanguage":"en-GB","@id":"https:\/\/news.truthjuice.co.uk\/#\/schema\/person\/image\/","url":"https:\/\/secure.gravatar.com\/avatar\/50e2c7869b4d2fcd7a3645c24b01bed4a88e8ed18aa2947c61c25e43732bea35?s=96&d=wavatar&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/50e2c7869b4d2fcd7a3645c24b01bed4a88e8ed18aa2947c61c25e43732bea35?s=96&d=wavatar&r=g","caption":"The Architect"},"sameAs":["http:\/\/www.truthjuice.co.uk"],"url":"https:\/\/news.truthjuice.co.uk\/index.php\/author\/the-architect\/"}]}},"_links":{"self":[{"href":"https:\/\/news.truthjuice.co.uk\/index.php\/wp-json\/wp\/v2\/posts\/2856","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/news.truthjuice.co.uk\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/news.truthjuice.co.uk\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/news.truthjuice.co.uk\/index.php\/wp-json\/wp\/v2\/users\/7"}],"replies":[{"embeddable":true,"href":"https:\/\/news.truthjuice.co.uk\/index.php\/wp-json\/wp\/v2\/comments?post=2856"}],"version-history":[{"count":1,"href":"https:\/\/news.truthjuice.co.uk\/index.php\/wp-json\/wp\/v2\/posts\/2856\/revisions"}],"predecessor-version":[{"id":3205,"href":"https:\/\/news.truthjuice.co.uk\/index.php\/wp-json\/wp\/v2\/posts\/2856\/revisions\/3205"}],"wp:attachment":[{"href":"https:\/\/news.truthjuice.co.uk\/index.php\/wp-json\/wp\/v2\/media?parent=2856"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/news.truthjuice.co.uk\/index.php\/wp-json\/wp\/v2\/categories?post=2856"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/news.truthjuice.co.uk\/index.php\/wp-json\/wp\/v2\/tags?post=2856"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}