{"id":53355,"date":"2012-10-02T14:30:12","date_gmt":"2012-10-02T14:30:12","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/immune-system-harnessed-to-improve-stem-cell-transplant-outcomes.php"},"modified":"2012-10-02T14:30:12","modified_gmt":"2012-10-02T14:30:12","slug":"immune-system-harnessed-to-improve-stem-cell-transplant-outcomes","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/stem-cell-therapy\/immune-system-harnessed-to-improve-stem-cell-transplant-outcomes.php","title":{"rendered":"Immune system harnessed to improve stem cell transplant outcomes"},"content":{"rendered":"<p><p>    ScienceDaily (Oct. 1, 2012)  A novel    therapy in the early stages of development at Virginia    Commonwealth University Massey Cancer Center shows promise in    providing lasting protection against the progression of    multiple myeloma following a stem cell transplant by making the    cancer cells easier targets for the immune system.  <\/p>\n<p>    Outlined in the British Journal of Hematology, the    Phase II clinical trial was led by Amir Toor, M.D.,    hematologist-oncologist in the Bone Marrow Transplant Program    and research member of the Developmental Therapeutics program    at VCU Massey Cancer Center. The multi-phased therapy first    treats patients with a combination of the drugs azacitidine and    lenalidomide. Azacitidine forces the cancer cells to express    proteins called cancer testis antigens (CTA) that immune system    cells called T-cell lymphocytes recognize as foreign. The    lenalidomide then boosts the production of T-cell lymphocytes.    Using a process called autologous lymphocyte infusion (ALI),    the T-cell lymphocytes are then extracted from the patient and    given back to them after they undergo a stem cell transplant to    restore the stem cells' normal function. Now able to recognize    the cancer cells as foreign, the T-cell lymphocytes can    potentially protect against a recurrence of multiple myeloma    following the stem cell transplant.  <\/p>\n<p>    \"Every cell in the body expresses proteins on their surface    that immune system cells scan like a barcode in order to    determine whether the cells are normal or if they are foreign.    Because multiple myeloma cells are spawned from bone marrow,    immune system cells cannot distinguish them from normal healthy    cells,\" says Toor. \"Azacitidine essentially changes the barcode    on the multiple myeloma cells, causing the immune system cells    to attack them,\" says Toor.  <\/p>\n<p>    The goal of the trial was to determine whether it was safe, and    even possible, to administer the two drugs in combination with    an ALI. In total, 14 patients successfully completed the    investigational drug therapy. Thirteen of the participants    successfully completed the investigational therapy and    underwent a stem cell transplant. Four patients had a complete    response, meaning no trace of multiple myeloma was detected,    and five patients had a very good partial response in which the    level of abnormal proteins in their blood decreased by 90    percent.  <\/p>\n<p>    In order to determine whether the azacitidine caused an    increased expression of CTA in the multiple myeloma cells, Toor    collaborated with Masoud Manjili, D.V.M., Ph.D., assistant    professor of microbiology and immunology at VCU Massey, to    conduct laboratory analyses on bone marrow biopsies taken from    trial participants before and after treatments. Each patient    tested showed an over-expression of multiple CTA, indicating    the treatment was successful at forcing the cancer cells to    produce these \"targets\" for the immune system.  <\/p>\n<p>    \"We designed this therapy in a way that could be replicated,    fairly inexpensively, at any facility equipped to perform a    stem cell transplant,\" says Toor. \"We plan to continue to    explore the possibilities of immunotherapies in multiple    myeloma patients in search for more effective therapies for    this very hard-to-treat disease.\"  <\/p>\n<p>    In addition to Manjili, Toor collaborated with John McCarty,    M.D., director of the Bone Marrow Transplant Program at VCU    Massey, and Harold Chung, M.D., William Clark, M.D., Catherine    Roberts, Ph.D., and Allison Hazlett, also all from Massey's    Bone Marrow Transplant Program; Kyle Payne, Maciej Kmieciak,    Ph.D., from Massey and the Department of Microbiology and    Immunology at VCU School of Medicine; Roy Sabo, Ph.D., from VCU    Department of Biostatistics and the Developmental Therapeutics    program at Massey; and David Williams, M.D., Ph.D., from the    Department of Pathology at VCU School of Medicine, co-director    of the Tissue and Data Acquisition and Analysis Core and    research member of the Developmental Therapeutics program at    Massey.  <\/p>\n<p>    Share this story on Facebook,    Twitter, and Google:  <\/p>\n<p>    Other social bookmarking and sharing tools:  <\/p>\n<p>    Story Source:  <\/p>\n<\/p>\n<p>More: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.sciencedaily.com\/releases\/2012\/10\/121001161444.htm\" title=\"Immune system harnessed to improve stem cell transplant outcomes\">Immune system harnessed to improve stem cell transplant outcomes<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> ScienceDaily (Oct. 1, 2012) A novel therapy in the early stages of development at Virginia Commonwealth University Massey Cancer Center shows promise in providing lasting protection against the progression of multiple myeloma following a stem cell transplant by making the cancer cells easier targets for the immune system. Outlined in the British Journal of Hematology, the Phase II clinical trial was led by Amir Toor, M.D., hematologist-oncologist in the Bone Marrow Transplant Program and research member of the Developmental Therapeutics program at VCU Massey Cancer Center <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/stem-cell-therapy\/immune-system-harnessed-to-improve-stem-cell-transplant-outcomes.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":[25],"tags":[],"class_list":["post-53355","post","type-post","status-publish","format-standard","hentry","category-stem-cell-therapy"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/53355"}],"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=53355"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/53355\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=53355"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=53355"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=53355"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}