<?xml version="1.0" encoding="utf-8"?>
<!DOCTYPE rss [<!ENTITY % HTMLlat1 PUBLIC "-//W3C//ENTITIES Latin 1 for XHTML//EN" "http://www.w3.org/TR/xhtml1/DTD/xhtml-lat1.ent">]>
<rss version="2.0" xml:base="http://www.caltechcancer.org">
<channel>
 <title>NSBCC: NanoSystems Biology Cancer Center - Project 2 Publications</title>
 <link>http://www.caltechcancer.org/taxonomy/term/97/0</link>
 <description></description>
 <language>en</language>
<item>
 <title>Project 2 Overview</title>
 <link>http://www.caltechcancer.org/node/64</link>
 <description>&lt;p&gt;&lt;span style=&quot;font-family: Arial&quot;&gt;&lt;b&gt;Single Cell&amp;nbsp; Micro/Nano-ImmunoChip for Cytotoxic T Lymphocyte Mediated Cancer Immunotherapy&lt;/b&gt;&lt;br /&gt; Refined through thousands of years of evolutionary advancement, the immune system has developed elegant strategies to defend the body against foreign pathogens and disease targets.&amp;nbsp; One of these mechanisms involve cytotoxic T lymphocytes (CTLs).&amp;nbsp; These T cells are a subset of white blood cells found in peripheral blood, lymph nodes, thymus and spleen.&amp;nbsp; They are distinguished from other cells types by their unique expression of the surface marker CD8. &amp;nbsp;&amp;nbsp;CTLs are so named for their ability either directly or indirectly through biochemical cascades to produce targeted cell death.&amp;nbsp; Each CTL expresses a slightly different T cell receptor (TCR), which recognizes a particular peptide sequence sequestered within the Major Histocompatibility complex (pMHC) on target cells.&amp;nbsp; All cells constantly present digested protein fragments representative of the cellular proteome as a pMHC.&amp;nbsp; The peptide is 7-10 amino acids long and provides sufficient information for the immune system to differentiate between the health state and identity of cells.&amp;nbsp; For example, cells whose control over their own translational machinery that has been usurped by viruses will display &amp;ldquo;foreign&amp;rdquo; pMHC, which the immune system recognizes as a breach and launches a series of responses eventually leading to the elimination of the disease target.&amp;nbsp; In similar fashion, T cells can recognize cancer antigens.&amp;nbsp; These peptide sequences are either unique (derived from oncogenetic mutations) or self antigens (derived from chronic activation of oncogenes or signal transduction pathways).&amp;nbsp; By maintaining a large dynamic library of different TCRs, a small population of CTLs exist that can induce cell death in cancer cells by recognizing cancer specific pMHC complexes.&amp;nbsp; The ability to harness and augment this specialized killer CTL to launch a persistent, effective, and specific anti-tumor response remains a promising goal in cancer immunology.&lt;/span&gt;&lt;/p&gt;</description>
 <category domain="http://www.caltechcancer.org/taxonomy/term/97">Project 2 Publications</category>
 <pubDate>Thu,  5 Jan 2006 13:11:54 -0800</pubDate>
</item>
</channel>
</rss>
