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type=\u0022text\/css\u0022 rel=\u0022stylesheet\u0022 href=\u0022\/\/d282kpwvnogo5m.cloudfront.net\/sites\/default\/files\/cdn\/css\/http\/css_Xg7z6oCTVgud_Q0huYz9x9iiD5H_2YPSJ5z2ZViSWdY.css\u0022 media=\u0022all\u0022 \/\u003E\n\u003Clink rel=\u0027stylesheet\u0027 type=\u0027text\/css\u0027 href=\u0027\/sites\/all\/modules\/contrib\/panels\/plugins\/layouts\/onecol\/onecol.css\u0027 \/\u003E\u003C\/head\u003E\u003Cbody\u003E\u003Cdiv class=\u0022panels-ajax-tab-panel panels-ajax-tab-panel-sageoa-tab-art\u0022\u003E\u003Cdiv class=\u0022panel-display panel-1col clearfix\u0022 \u003E\n  \u003Cdiv class=\u0022panel-panel panel-col\u0022\u003E\n    \u003Cdiv\u003E\u003Cdiv class=\u0022panel-pane pane-highwire-markup\u0022 \u003E\n  \n      \n  \n  \u003Cdiv class=\u0022pane-content\u0022\u003E\n    \u003Cdiv class=\u0022highwire-markup\u0022\u003E\u003Cdiv xmlns=\u0022http:\/\/www.w3.org\/1999\/xhtml\u0022 id=\u0022content-block-markup\u0022 xmlns:xhtml=\u0022http:\/\/www.w3.org\/1999\/xhtml\u0022\u003E\u003Cdiv class=\u0022article fulltext-view \u0022\u003E\u003Cspan class=\u0022highwire-journal-article-marker-start\u0022\u003E\u003C\/span\u003E\u003Cdiv class=\u0022section abstract\u0022 id=\u0022abstract-1\u0022\u003E\u003Ch2\u003ESummary\u003C\/h2\u003E\n            \u003Cp id=\u0022p-1\u0022\u003EAs regenerative medicine moves into the 21st century, its promise to better treat diseases by using the body\u0027s own tissues and systems to repair dysfunction is increasingly becoming a reality. Rheumatologists, like physicians across all specialties, will need to recognize and understand the way in which stem cells function in diseases and how these cells can be harvested and harnessed to provide ever improved treatment options. This article looks at ways adult stem cells being used in rheumatic diseases, and some of the key regulatory issues related to the use of embryonic stem cells.\u003C\/p\u003E\n         \u003C\/div\u003E\u003Cul class=\u0022kwd-group\u0022\u003E\u003Cli class=\u0022kwd\u0022\u003ERheumatological Autoimmune Disorders\u003C\/li\u003E\u003C\/ul\u003E\u003Cul class=\u0022kwd-group clinical-trial\u0022\u003E\u003Cli class=\u0022kwd\u0022\u003ERheumatology\u003C\/li\u003E\u003Cli class=\u0022kwd\u0022\u003ERheumatological Autoimmune Disorders\u003C\/li\u003E\u003C\/ul\u003E\u003Cp id=\u0022p-2\u0022\u003EAs regenerative medicine moves into the 21st century, its promise to better treat diseases by using the body\u0027s own tissues and systems to repair dysfunction is increasingly becoming a reality. Rheumatologists, like physicians across all specialties, will need to recognize and understand the way in which stem cells function in diseases and how these cells can be harvested and harnessed to provide ever improved treatment options. How are adult stem cells being used in rheumatic diseases? What are some of the key regulatory issues related to the use of embryonic stem cells?\u003C\/p\u003E\u003Cdiv class=\u0022section\u0022 id=\u0022sec-1\u0022\u003E\n         \u003Ch2 class=\u0022\u0022\u003ESTEM CELLS AND THEIR USE IN RHEUMATIC DISEASES: ADULT STEM CELLS\u003C\/h2\u003E\n         \u003Cp id=\u0022p-3\u0022\u003EAlan Tyndall, MD, University of Basel, Basel, Switzerland, presented current data on the application of adult or postnatal stem cells in autoimmune diseases. He focused the talk on the hematopoietic stem cell transplantation (HSCT) program that has been underway for about the past 15 years, as well as the newer, still evolving program in mesenchymal stromal cell transplantation.\u003C\/p\u003E\n      \u003C\/div\u003E\u003Cdiv class=\u0022section\u0022 id=\u0022sec-2\u0022\u003E\n         \u003Ch2 class=\u0022\u0022\u003EHEMATOPOIETIC STEM CELL TRANSPLANTATION PROGRAM\u003C\/h2\u003E\n         \u003Cp id=\u0022p-4\u0022\u003ESince September 2011, about 1500 patients in Europe have received HSCT as listed on the European Group for Blood and Marrow Transplantation Registry. Most of these patients have undergone transplantation for multiple sclerosis (n=476) followed by connective tissue disease (n=427). In the United States, \u223c500 patients with severe autoimmune diseases have received transplantation. The concept of HSCT transplantation for autoimmune disease is to replace ablated immune and hematopoietic systems to allow deep immunosuppression that may then permit resetting autoimmunity.\u003C\/p\u003E\n         \u003Cp id=\u0022p-5\u0022\u003ECurrently, four prospective randomized clinical trials have been performed to evaluate the efficacy of HSCT for autoimmune diseases. Three of these trials evaluate the efficacy of HSCT for patients with systemic sclerosis (scleroderma), and one trial for Crohn\u0027s disease (\u003Ca id=\u0022xref-table-wrap-1-1\u0022 class=\u0022xref-table\u0022 href=\u0022#T1\u0022\u003ETable 1\u003C\/a\u003E).\u003C\/p\u003E\n         \u003Cp id=\u0022p-6\u0022\u003EFor example, the ASTIS trial [\u003Ca href=\u0022\/external-ref?link_type=ISRCTN\u0026amp;access_num=ISRCTN54371254\u0022 class=\u0022external-ref external-ref-type-isrctn\u0022\u003EISRCTN54371254\u003C\/a\u003E] is a multicenter, multinational, investigator-initiated, prospective trial that has enrolled 156 patients with poor prognosis early diffuse cutaneous systemic sclerosis [van Laar JM et al. EULAR 2012 (abstr LB0002)]. Patients were randomized to HSCT (n=79) or control (n=77). As of May 2012, the study has shown that patients treated with HSCT had significantly better long-term, event-free, and overall survival despite \u223c10% treatment-related mortality compared with controls (who received 12 months of intravenous cyclophosphamide). The study also found smoking status as a determinant of event-free and overall survival after HSCT, with a reduction in event-free and overall survival in smokers. Secondary outcomes of the study also showed that HSCT patients felt better overall than controls based on measures such as mRSS as well as other clinical outcomes.\u003C\/p\u003E\n         \u003Cdiv id=\u0022T1\u0022 class=\u0022table pos-float\u0022\u003E\u003Cdiv class=\u0022table-inline\u0022\u003E\u003Cdiv class=\u0022callout\u0022\u003E\u003Cspan\u003EView this table:\u003C\/span\u003E\u003Cul class=\u0022callout-links\u0022\u003E\u003Cli class=\u00220 first\u0022\u003E\u003Ca href=\u0022\/\u0022 class=\u0022table-expand-inline\u0022 data-table-url=\u0022\/highwire\/markup\/13849\/expansion?postprocessors=highwire_figures%2Chighwire_math%2Chighwire_inline_linked_media%2Chighwire_embed\u0026amp;table-expand-inline=1\u0022 html=\u00221\u0022 fragment=\u0022#\u0022 external=\u00221\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EView inline\u003C\/a\u003E\u003C\/li\u003E\u003Cli class=\u00221\u0022\u003E\u003Ca href=\u0022\/highwire\/markup\/13849\/expansion?width=1000\u0026amp;height=500\u0026amp;iframe=true\u0026amp;postprocessors=highwire_figures%2Chighwire_math%2Chighwire_inline_linked_media\u0022 class=\u0022colorbox colorbox-load table-expand-popup\u0022 rel=\u0022gallery-fragment-tables\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EView popup\u003C\/a\u003E\u003C\/li\u003E\u003Cli class=\u00222 last\u0022\u003E\u003Ca href=\u0022\/highwire\/powerpoint\/13849\u0022 class=\u0022highwire-figure-link highwire-figure-link-ppt\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EDownload powerpoint\u003C\/a\u003E\u003C\/li\u003E\u003C\/ul\u003E\u003C\/div\u003E\u003C\/div\u003E\u003Cdiv class=\u0022table-caption\u0022\u003E\u003Cspan class=\u0022table-label\u0022\u003ETable 1.\u003C\/span\u003E \n               \u003Cp id=\u0022p-7\u0022 class=\u0022first-child\u0022\u003EClinical Trials to Evaluate Efficacy of HSCT for Autoimmune Diseases\u003C\/p\u003E\n            \u003Cdiv class=\u0022sb-div caption-clear\u0022\u003E\u003C\/div\u003E\u003C\/div\u003E\u003C\/div\u003E\n         \u003Cp id=\u0022p-8\u0022\u003EOverall, Dr. Tyndall emphasized that what has been learned over the past 15 years is that it is possible to reset autoimmunity in some patients, and that the responses are durable, including in some cases loss of autoantibodies, and not just due to long-term immunosuppression. He also emphasized that there will always be some treatment-related-mortality and toxicity, which, he said may be possible to reduce by better patient selection (eg, selecting patients who do not smoke). Finally, he emphasized the need to transplant before irreversible organ damage occurs.\u003C\/p\u003E\n      \u003C\/div\u003E\u003Cdiv class=\u0022section\u0022 id=\u0022sec-3\u0022\u003E\n         \u003Ch2 class=\u0022\u0022\u003EMESENCHYMAL STROMAL CELL TRANSPLANTATION\u003C\/h2\u003E\n         \u003Cp id=\u0022p-9\u0022\u003EA newer, still evolving type of stem cell transplantation is the use of mesenchymal stromal cells for transplantation for severe autoimmune diseases. The promise of the use of these cells for transplantation is based on the concept that mesenchymal stromal cells home to inflamed tissue, provide an anti-inflammatory effect, and may be able to repair damaged tissue. A number of Phase 1 and 2 uncontrolled clinical trials are underway using these cells in autoimmune disease, and current data suggest that acute toxicity appears low. However, long-term safety is not known and the current evidence suggests the need for tumour surveillance as well as adequately powered controlled studies.\u003C\/p\u003E\n      \u003C\/div\u003E\u003Cdiv class=\u0022section\u0022 id=\u0022sec-4\u0022\u003E\n         \u003Ch2 class=\u0022\u0022\u003EREGULATION OF EMBRYONIC (PLURIPOTENT) STEM CELLS\u003C\/h2\u003E\n         \u003Cp id=\u0022p-10\u0022\u003EUnlike adult stem cells, investigation into the use of pluripotent stem cells for rheumatic diseases as well as other diseases is very young with only three ongoing trials of these cells currently under way in the United States. According to Melissa Carpenter, PhD, Carpenter Group Consulting, Seattle, Washington, USA, key issues regarding these cells and their potential therapeutic use revolve around regulation of stem cell products due to their fundamental characteristic of living cells. She highlighted the unique challenge of developing cell products from these cells and preclinical testing of these products. Among the challenges of developing pluripotent stem cell products are safety concerns due to the cell\u0027s unlimited proliferative capacity (which raises concerns about their stability over the long term) as well as their pluripotency (which raises concerns about teratoma formation).\u003C\/p\u003E\n         \u003Cp id=\u0022p-11\u0022\u003EChallenges to preclinical testing of pluripotent stem cell products include the lack of a standard set of preclinical tests and testing parameters applicable to all products, and the need for a case-by-case strategy for preclinical regulatory testing based on the diversity and biological properties of products derived from these cells. \u003Ca id=\u0022xref-table-wrap-2-1\u0022 class=\u0022xref-table\u0022 href=\u0022#T2\u0022\u003ETable 2\u003C\/a\u003E highlights key issues that regulatory agencies need addressed prior to approving preclinical study designs.\u003C\/p\u003E\n         \u003Cdiv id=\u0022T2\u0022 class=\u0022table pos-float\u0022\u003E\u003Cdiv class=\u0022table-inline\u0022\u003E\u003Cdiv class=\u0022callout\u0022\u003E\u003Cspan\u003EView this table:\u003C\/span\u003E\u003Cul class=\u0022callout-links\u0022\u003E\u003Cli class=\u00220 first\u0022\u003E\u003Ca href=\u0022\/\u0022 class=\u0022table-expand-inline\u0022 data-table-url=\u0022\/highwire\/markup\/13850\/expansion?postprocessors=highwire_figures%2Chighwire_math%2Chighwire_inline_linked_media%2Chighwire_embed\u0026amp;table-expand-inline=1\u0022 html=\u00221\u0022 fragment=\u0022#\u0022 external=\u00221\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EView inline\u003C\/a\u003E\u003C\/li\u003E\u003Cli class=\u00221\u0022\u003E\u003Ca href=\u0022\/highwire\/markup\/13850\/expansion?width=1000\u0026amp;height=500\u0026amp;iframe=true\u0026amp;postprocessors=highwire_figures%2Chighwire_math%2Chighwire_inline_linked_media\u0022 class=\u0022colorbox colorbox-load table-expand-popup\u0022 rel=\u0022gallery-fragment-tables\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EView popup\u003C\/a\u003E\u003C\/li\u003E\u003Cli class=\u00222 last\u0022\u003E\u003Ca href=\u0022\/highwire\/powerpoint\/13850\u0022 class=\u0022highwire-figure-link highwire-figure-link-ppt\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EDownload powerpoint\u003C\/a\u003E\u003C\/li\u003E\u003C\/ul\u003E\u003C\/div\u003E\u003C\/div\u003E\u003Cdiv class=\u0022table-caption\u0022\u003E\u003Cspan class=\u0022table-label\u0022\u003ETable 2.\u003C\/span\u003E \n               \u003Cp id=\u0022p-12\u0022 class=\u0022first-child\u0022\u003EIssues for Approving Preclinical Study Designs\u003C\/p\u003E\n            \u003Cdiv class=\u0022sb-div caption-clear\u0022\u003E\u003C\/div\u003E\u003C\/div\u003E\u003C\/div\u003E\n         \u003Cp id=\u0022p-13\u0022\u003EVarious kinds of preclinical study designs include studies to assess the pharmacology and proof-of-concept of pluripotent stem cell products in relevant animal models of disease, studies to assess safety and toxicity in healthy animals, and studies with a hybrid pharmacology-toxicology study design.\u003C\/p\u003E\n         \u003Cp id=\u0022p-14\u0022\u003EOverall, Dr. Carpenter said that despite the many hurdles to develop pluripotent stem cell products and get them approved for preclinical testing, the field is moving very quickly.\u003C\/p\u003E\n      \u003C\/div\u003E\u003Cul class=\u0022copyright-statement\u0022\u003E\u003Cli class=\u0022fn\u0022 id=\u0022copyright-statement-1\u0022\u003E\u00a9 2013 MD Conference Express\u00ae\u003C\/li\u003E\u003C\/ul\u003E\u003Cspan class=\u0022highwire-journal-article-marker-end\u0022\u003E\u003C\/span\u003E\u003C\/div\u003E\u003Cspan id=\u0022related-urls\u0022\u003E\u003C\/span\u003E\u003C\/div\u003E\u003Ca href=\u0022http:\/\/mdc.sagepub.com\/content\/13\/18\/36.abstract\u0022 class=\u0022hw-link hw-link-article-abstract\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EView Summary\u003C\/a\u003E\u003C\/div\u003E  \u003C\/div\u003E\n\n  \n  \u003C\/div\u003E\n\u003C\/div\u003E\n  \u003C\/div\u003E\n\u003C\/div\u003E\n\u003C\/div\u003E\u003Cscript type=\u0022text\/javascript\u0022 src=\u0022http:\/\/mdc.sagepub.com\/sites\/all\/modules\/highwire\/highwire\/plugins\/highwire_markup_process\/js\/highwire_openurl.js?nzo761\u0022\u003E\u003C\/script\u003E\n\u003Cscript type=\u0022text\/javascript\u0022 src=\u0022http:\/\/mdc.sagepub.com\/sites\/all\/modules\/highwire\/highwire\/plugins\/highwire_markup_process\/js\/highwire_tables.js?nzo761\u0022\u003E\u003C\/script\u003E\n\u003C\/body\u003E\u003C\/html\u003E"}