<?xml version="1.0" encoding="ISO-8859-1"?>

<rdf:RDF
 xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
 xmlns="http://purl.org/rss/1.0/"
 xmlns:taxo="http://purl.org/rss/1.0/modules/taxonomy/"
 xmlns:dc="http://purl.org/dc/elements/1.1/"
 xmlns:syn="http://purl.org/rss/1.0/modules/syndication/"
 xmlns:prism="http://purl.org/rss/1.0/modules/prism/"
 xmlns:admin="http://webns.net/mvcb/"
>

<channel rdf:about="http://bloodjournal.hematologylibrary.org">
<title>Blood TRANSFUSION MEDICINE</title>
<link>http://bloodjournal.hematologylibrary.org</link>
<description>Blood RSS feed -- recent TRANSFUSION MEDICINE articles</description>
<prism:eIssn>1528-0020</prism:eIssn>
<prism:publicationName>Blood</prism:publicationName>
<prism:issn>0006-4971</prism:issn>
<items>
 <rdf:Seq>
  <rdf:li rdf:resource="http://bloodjournal.hematologylibrary.org/cgi/content/short/111/7/3880?rss=1" />
 </rdf:Seq>
</items>
<image rdf:resource="http://bloodjournal.hematologylibrary.org/icons/banner/title.gif" />
</channel>

<image rdf:about="http://bloodjournal.hematologylibrary.org/icons/banner/title.gif">
<title>Blood</title>
<url>http://bloodjournal.hematologylibrary.org/icons/banner/title.gif</url>
<link>http://bloodjournal.hematologylibrary.org</link>
</image>

<item rdf:about="http://bloodjournal.hematologylibrary.org/cgi/content/short/111/7/3880?rss=1">
<title><![CDATA[The TNF (-308A) polymorphism is associated with microchimerism in transfused trauma patients]]></title>
<link>http://bloodjournal.hematologylibrary.org/cgi/content/short/111/7/3880?rss=1</link>
<description><![CDATA[
<p>Microchimerism (MC), defined as the persistence of allogeneic cells at low concentrations, is well documented in transfused trauma patients. We hypothesized that genetic polymorphisms linked to cytokine production could contribute to trauma-induced immune modulation and development of microchimerism after transfusion of trauma patients. We used high-throughput SYBR-green-based genotyping of single nucleotide polymorphisms (SNPs) to characterize 59 transfused trauma patients, with MC (n = 30) and without MC (n = 29), for 4 functionally significant SNPs: <I>TNF</I> (&ndash;308), <I>IL 10</I> (&ndash;1082), <I>IFNG</I> (+874), and <I>TGFB</I>1 (+915). We then compared likelihood for development of MC and the magnitude of immune suppression among subjects with and without these selected immune response SNPs. We identified a significant association between <I>TNF</I> (&ndash;308A) SNP and both development of MC and diminished immune responsiveness. Hence predisposing genetic factors may explain, in part, why only a subset of trauma patients develops transfusion-associated microchimerism.</p>
]]></description>
<dc:creator><![CDATA[Gill, R. M., Lee, T.-H., Utter, G. H., Reed, W. F., Wen, L., Chafets, D., Busch, M. P.]]></dc:creator>
<dc:date>2008-03-24</dc:date>
<dc:subject><![CDATA[Hematopoiesis, Immunobiology, Transfusion Medicine, Transplantation, Brief Reports]]></dc:subject>
<dc:identifier>info:doi/10.1182/blood-2007-08-107144</dc:identifier>
<dc:title><![CDATA[The TNF (-308A) polymorphism is associated with microchimerism in transfused trauma patients]]></dc:title>
<dc:publisher>American Society of Hematology</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>111</prism:volume>
<prism:endingPage>3883</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>3880</prism:startingPage>
<prism:section>TRANSFUSION MEDICINE</prism:section>
</item>

</rdf:RDF>