{"id":135939,"date":"2014-05-22T17:52:43","date_gmt":"2014-05-22T21:52:43","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/fda-approves-first-molecular-gene-based-test-to-determine-red-blood-cell-types-in-transfusion-medicine.php"},"modified":"2014-05-22T17:52:43","modified_gmt":"2014-05-22T21:52:43","slug":"fda-approves-first-molecular-gene-based-test-to-determine-red-blood-cell-types-in-transfusion-medicine","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/molecular-medicine\/fda-approves-first-molecular-gene-based-test-to-determine-red-blood-cell-types-in-transfusion-medicine.php","title":{"rendered":"FDA approves first molecular (gene-based) test to determine red blood cell types in transfusion medicine"},"content":{"rendered":"<p><p>    The U.S. Food and Drug Administration today approved the    Immucor PreciseType Human Erythrocyte Antigen (HEA) Molecular    BeadChip Test  the first FDA-approved molecular assay used in    transfusion medicine to assist in determining blood    compatibility. The assay can be used to determine donor and    patient non-ABO\/non-RhD (non-ABO) red blood cell types in the    United States.  <\/p>\n<p>    The surfaces of red blood cells display minor blood group    antigens in addition to the major ABO blood group antigens.    Some people develop antibodies to non-ABO antigens following    transfusion or pregnancy. This is especially true in people who    may receive repeated blood transfusions, such as those with    sickle cell disease. The development of such antibodies can    cause red blood cell destruction if red blood cells with the    corresponding antigens are later transfused.  <\/p>\n<p>    Development of antibodies to non-ABO antigens can be prevented    by selecting blood that is better matched to the patients    non-ABO antigens. In addition, when a potential transfusion    recipient has a known antibody that causes red blood cell    destruction, red blood cells that are negative for the    corresponding antigen must be found. The identification of red    blood cell antigens has traditionally been performed by    serological typing. This involves testing blood with reagents    (antisera) that are specific for the antigens for which the    blood is being tested. However, specific antisera may be scarce    or unavailable. The Immucor PreciseType HEA Molecular BeadChip    Test provides a new method for determining non-ABO antigens on    red blood cells.  <\/p>\n<p>    The approval of the Immucor PreciseType HEA Molecular BeadChip    Test provides an alternative to serological typing and may    enhance patient care in certain situations, said Karen    Midthun, M.D., director of the FDAs Center for Biologics    Evaluation and Research.  <\/p>\n<p>    The Immucor PreciseType HEA Molecular BeadChip Test works by    detecting genes that govern the expression of 36 antigens that    can appear on the surface of red blood cells. The test uses    thousands of coded beads that bind with the genes coding for    non-ABO red blood cell antigens that are present in a blood    sample. A light signal is generated from each bead that has    captured a specific gene. Accompanying computer software    decodes the light signals and reports which antigens are    predicted to be present on the red cells based on the genes    that are detected.  <\/p>\n<p>    A study was conducted to compare the typing results of the    PreciseType HEA Molecular BeadChip Test with licensed    serological reagents and DNA sequencing. The results    demonstrated comparable performance between the methods.  <\/p>\n<p>    The product was brought before the     FDAs Blood Products Advisory Committee on March 18, 2014.    After reviewing the relevant information, the committee    concluded that the data provided reasonable assurance that the    Immucor PreciseType HEA Molecular BeadChip Test is safe and    effective for its intended use.  <\/p>\n<p>    The Immucor PreciseType HEA Molecular BeadChip Test is    manufactured by BioArray Solutions Ltd. of Warren, New Jersey.  <\/p>\n<p>    The FDA, an agency within the U.S. Department of Health and    Human Services, protects the public health by assuring the    safety, effectiveness, and security of human and veterinary    drugs, vaccines and other biological products for human use,    and medical devices. The agency also is responsible for the    safety and security of our nation's food supply, cosmetics,    dietary supplements, products that give off electronic    radiation, and for regulating tobacco products.  <\/p>\n<p>    ###  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Original post: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.fda.gov\/NewsEvents\/Newsroom\/PressAnnouncements\/ucm398371.htm\/RK=0\/RS=AAUgg0hzOpQO4_99OTcQql6MYzE-\" title=\"FDA approves first molecular (gene-based) test to determine red blood cell types in transfusion medicine\">FDA approves first molecular (gene-based) test to determine red blood cell types in transfusion medicine<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> The U.S. Food and Drug Administration today approved the Immucor PreciseType Human Erythrocyte Antigen (HEA) Molecular BeadChip Test the first FDA-approved molecular assay used in transfusion medicine to assist in determining blood compatibility. The assay can be used to determine donor and patient non-ABO\/non-RhD (non-ABO) red blood cell types in the United States.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/molecular-medicine\/fda-approves-first-molecular-gene-based-test-to-determine-red-blood-cell-types-in-transfusion-medicine.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":[26],"tags":[],"class_list":["post-135939","post","type-post","status-publish","format-standard","hentry","category-molecular-medicine"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/135939"}],"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=135939"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/135939\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=135939"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=135939"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=135939"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}