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<title>Nature Immunology - Issue - nature.com science feeds</title>
<description>Nature Immunology is a multidisciplinary journal that publishes papers of the highest quality and significance in all areas of immunology. Priority is given to work that provides fundamental insight into the workings of the immune system. Areas covered include, but are not limited to, innate immunity and inflammation; development; immune receptors, signaling and apoptosis; antigen presentation; gene regulation and recombination; cellular and systemic immunity; vaccines; immune tolerance; autoimmunity and tumor immunology, microbial immunopathology; and transplantation.</description>
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<dc:publisher>Nature Publishing Group</dc:publisher>
<dc:language>en</dc:language>
<dc:rights>© 2009 Nature Publishing Group</dc:rights>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:issn>1529-2908</prism:issn>
<prism:eIssn>1529-2916</prism:eIssn>
<prism:copyright>© 2009 Nature Publishing Group</prism:copyright>
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<title>Nature Immunology</title>
<url>http://www.nature.com/includes/rj_globnavimages/ni_logo.gif</url>
<link>http://www.nature.com/ni/</link>
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<item rdf:about="http://dx.doi.org/10.1038/ni1209-1223">
<title>Science: a common language</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/-4tv84SkTgA/ni1209-1223</link>
<description>Science and technology can be used to build relations between countries. Thus, scientific diplomacy is becoming increasingly important.</description>
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<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>Science: a common language</b>
</p>
<p>Nature Immunology 10, 1223 (2009). <a href="http://dx.doi.org/10.1038/ni1209-1223">doi:10.1038/ni1209-1223</a>
</p>
<p>Science and technology can be used to build relations between countries. Thus, scientific diplomacy is becoming increasingly important.</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/-4tv84SkTgA" height="1" width="1"/>]]></content:encoded>
<dc:title>Science: a common language</dc:title>
<dc:identifier>doi:10.1038/ni1209-1223</dc:identifier>
<dc:source>Nature Immunology 10, 1223 (2009)</dc:source>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:doi>10.1038/ni1209-1223</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni1209-1223</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Editorial</prism:section>
<prism:startingPage>1223</prism:startingPage>
<prism:endingPage>1223</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/ni1209-1223</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/ni1209-1225">
<title>Data management: it starts at the bench</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/ouHtrbyEj3k/ni1209-1225</link>
<description>Data management has been neglected but should be made an integral activity in all research laboratories. Chaussabel and colleagues discuss how to implement this at the bench.</description>
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>Data management: it starts at the bench</b>
</p>
<p>Nature Immunology 10, 1225 (2009). <a href="http://dx.doi.org/10.1038/ni1209-1225">doi:10.1038/ni1209-1225</a>
</p>
<p>Authors: Damien Chaussabel, Hideki Ueno, Jacques Banchereau &amp; Charles Quinn</p>
<p>Data management has been neglected but should be made an integral activity in all research laboratories. Chaussabel and colleagues discuss how to implement this at the bench.</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/ouHtrbyEj3k" height="1" width="1"/>]]></content:encoded>
<dc:title>Data management: it starts at the bench</dc:title>
<dc:creator>Damien Chaussabel</dc:creator>
<dc:creator>Hideki Ueno</dc:creator>
<dc:creator>Jacques Banchereau</dc:creator>
<dc:creator>Charles Quinn</dc:creator>
<dc:identifier>doi:10.1038/ni1209-1225</dc:identifier>
<dc:source>Nature Immunology 10, 1225 (2009)</dc:source>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:doi>10.1038/ni1209-1225</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni1209-1225</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Commentary</prism:section>
<prism:startingPage>1225</prism:startingPage>
<prism:endingPage>1227</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/ni1209-1225</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/ni1209-1229">
<title>MicroRNA-managing the TH-17 inflammatory response</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/iWnuOme8J2g/ni1209-1229</link>
<description>The differentiation of interleukin 17–producing helper T cells is controlled by a complex network of cytokines, signaling pathways and transcription factors. Regulation by microRNA particles can now be added to this list.</description>
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>MicroRNA-managing the TH-17 inflammatory response</b>
</p>
<p>Nature Immunology 10, 1229 (2009). <a href="http://dx.doi.org/10.1038/ni1209-1229">doi:10.1038/ni1209-1229</a>
</p>
<p>Authors: Aaron J Martin, Liang Zhou &amp; Stephen D Miller</p>
<p>The differentiation of interleukin 17&#8211;producing helper T cells is controlled by a complex network of cytokines, signaling pathways and transcription factors. Regulation by microRNA particles can now be added to this list.</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/iWnuOme8J2g" height="1" width="1"/>]]></content:encoded>
<dc:title>MicroRNA-managing the TH-17 inflammatory response</dc:title>
<dc:creator>Aaron J Martin</dc:creator>
<dc:creator>Liang Zhou</dc:creator>
<dc:creator>Stephen D Miller</dc:creator>
<dc:identifier>doi:10.1038/ni1209-1229</dc:identifier>
<dc:source>Nature Immunology 10, 1229 (2009)</dc:source>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:doi>10.1038/ni1209-1229</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni1209-1229</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>News and Views</prism:section>
<prism:startingPage>1229</prism:startingPage>
<prism:endingPage>1231</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/ni1209-1229</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/ni1209-1231">
<title>T cells need Nod too?</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/FV82QgQJMOo/ni1209-1231</link>
<description>Nucleotide-binding oligomerization domain 2 (Nod2) is required for sensing of intracellular bacteria and subsequent inflammatory responses. Unexpectedly, new evidence suggests that Nod2 influences T helper cell signaling, proliferation and differentiation and effector responses against Toxoplasma gondii.</description>
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>T cells need Nod too?</b>
</p>
<p>Nature Immunology 10, 1231 (2009). <a href="http://dx.doi.org/10.1038/ni1209-1231">doi:10.1038/ni1209-1231</a>
</p>
<p>Authors: Shahram Salek-Ardakani &amp; Michael Croft</p>
<p>Nucleotide-binding oligomerization domain 2 (Nod2) is required for sensing of intracellular bacteria and subsequent inflammatory responses. Unexpectedly, new evidence suggests that Nod2 influences T helper cell signaling, proliferation and differentiation and effector responses against Toxoplasma gondii.</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/FV82QgQJMOo" height="1" width="1"/>]]></content:encoded>
<dc:title>T cells need Nod too?</dc:title>
<dc:creator>Shahram Salek-Ardakani</dc:creator>
<dc:creator>Michael Croft</dc:creator>
<dc:identifier>doi:10.1038/ni1209-1231</dc:identifier>
<dc:source>Nature Immunology 10, 1231 (2009)</dc:source>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:doi>10.1038/ni1209-1231</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni1209-1231</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>News and Views</prism:section>
<prism:startingPage>1231</prism:startingPage>
<prism:endingPage>1233</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/ni1209-1231</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/ni1209-1233">
<title>B cell memory: how to start and when to end</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/zGfVu4FhcCQ/ni1209-1233</link>
<description>Antigen-driven selection in germinal centers lays the foundation of effective B cell memory. Two reports in this issue reveal novel mechanisms that control effective formation of germinal centers and their long-term persistence in vivo.</description>
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>B cell memory: how to start and when to end</b>
</p>
<p>Nature Immunology 10, 1233 (2009). <a href="http://dx.doi.org/10.1038/ni1209-1233">doi:10.1038/ni1209-1233</a>
</p>
<p>Authors: Nadege Pelletier &amp; Michael G McHeyzer-Williams</p>
<p>Antigen-driven selection in germinal centers lays the foundation of effective B cell memory. Two reports in this issue reveal novel mechanisms that control effective formation of germinal centers and their long-term persistence in vivo.</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/zGfVu4FhcCQ" height="1" width="1"/>]]></content:encoded>
<dc:title>B cell memory: how to start and when to end</dc:title>
<dc:creator>Nadege Pelletier</dc:creator>
<dc:creator>Michael G McHeyzer-Williams</dc:creator>
<dc:identifier>doi:10.1038/ni1209-1233</dc:identifier>
<dc:source>Nature Immunology 10, 1233 (2009)</dc:source>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:doi>10.1038/ni1209-1233</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni1209-1233</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>News and Views</prism:section>
<prism:startingPage>1233</prism:startingPage>
<prism:endingPage>1235</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/ni1209-1233</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/ni1209-1236">
<title>Research Highlights</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/36AyMBNyk1s/ni1209-1236</link>
<description />
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>Research Highlights</b>
</p>
<p>Nature Immunology 10, 1236 (2009). <a href="http://dx.doi.org/10.1038/ni1209-1236">doi:10.1038/ni1209-1236</a>
</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/36AyMBNyk1s" height="1" width="1"/>]]></content:encoded>
<dc:title>Research Highlights</dc:title>
<dc:identifier>doi:10.1038/ni1209-1236</dc:identifier>
<dc:source>Nature Immunology 10, 1236 (2009)</dc:source>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:doi>10.1038/ni1209-1236</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni1209-1236</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlights</prism:section>
<prism:startingPage>1236</prism:startingPage>
<prism:endingPage>1236</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/ni1209-1236</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/ni.1822">
<title>Dendritic cell subsets in primary and secondary T cell responses at body surfaces</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/6xZ7d9hiJs0/ni.1822</link>
<description />
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>Dendritic cell subsets in primary and secondary T cell responses at body surfaces</b>
</p>
<p>Nature Immunology 10, 1237 (2009). <a href="http://dx.doi.org/10.1038/ni.1822">doi:10.1038/ni.1822</a>
</p>
<p>Authors: William R Heath &amp; Francis R Carbone</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/6xZ7d9hiJs0" height="1" width="1"/>]]></content:encoded>
<dc:title>Dendritic cell subsets in primary and secondary T cell responses at body surfaces</dc:title>
<dc:creator>William R Heath</dc:creator>
<dc:creator>Francis R Carbone</dc:creator>
<dc:identifier>doi:10.1038/ni.1822</dc:identifier>
<dc:source>Nature Immunology 10, 1237 (2009)</dc:source>
<dc:date>2009-11-16</dc:date>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:publicationDate>2009-11-16</prism:publicationDate>
<prism:doi>10.1038/ni.1822</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni.1822</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>1237</prism:startingPage>
<prism:endingPage>1244</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/ni.1822</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/ni.1813">
<title>Structural basis of receptor sharing by interleukin 17 cytokines</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/4wgM2tKW8Ek/ni.1813</link>
<description>The interleukin 17 (IL-17) family includes six cytokines and five receptors. Garcia and co-workers solve the crystal structure of the receptor IL-17RA bound to IL-17F and suggest that IL-17RA may act as a shared subunit among multiple IL-17 receptor complexes.</description>
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>Structural basis of receptor sharing by interleukin 17 cytokines</b>
</p>
<p>Nature Immunology 10, 1245 (2009). <a href="http://dx.doi.org/10.1038/ni.1813">doi:10.1038/ni.1813</a>
</p>
<p>Authors: Lauren K Ely, Suzanne Fischer &amp; K Christopher Garcia</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/4wgM2tKW8Ek" height="1" width="1"/>]]></content:encoded>
<dc:title>Structural basis of receptor sharing by interleukin 17 cytokines</dc:title>
<dc:creator>Lauren K Ely</dc:creator>
<dc:creator>Suzanne Fischer</dc:creator>
<dc:creator>K Christopher Garcia</dc:creator>
<dc:identifier>doi:10.1038/ni.1813</dc:identifier>
<dc:source>Nature Immunology 10, 1245 (2009)</dc:source>
<dc:date>2009-10-18</dc:date>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:publicationDate>2009-10-18</prism:publicationDate>
<prism:doi>10.1038/ni.1813</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni.1813</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Article</prism:section>
<prism:startingPage>1245</prism:startingPage>
<prism:endingPage>1251</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/ni.1813</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/ni.1798">
<title>MicroRNA miR-326 regulates TH-17 differentiation and is associated with the pathogenesis of multiple sclerosis</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/veIrjl7YyfQ/ni.1798</link>
<description>Interleukin 17 (IL-17)-producing helper T cells (TH-17 cells) are associated with the pathogenesis of multiple sclerosis. Pei and colleagues have now identified a TH-17 cell–associated microRNA, miR-326, whose expression correlates with disease severity in patients with multiple sclerosis and mice with experimental autoimmune encephalomyelitis.</description>
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>MicroRNA miR-326 regulates TH-17 differentiation and is associated with the pathogenesis of multiple sclerosis</b>
</p>
<p>Nature Immunology 10, 1252 (2009). <a href="http://dx.doi.org/10.1038/ni.1798">doi:10.1038/ni.1798</a>
</p>
<p>Authors: Changsheng Du, Chang Liu, Jiuhong Kang, Guixian Zhao, Zhiqiang Ye, Shichao Huang, Zhenxin Li, Zhiying Wu &amp; Gang Pei</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/veIrjl7YyfQ" height="1" width="1"/>]]></content:encoded>
<dc:title>MicroRNA miR-326 regulates TH-17 differentiation and is associated with the pathogenesis of multiple sclerosis</dc:title>
<dc:creator>Changsheng Du</dc:creator>
<dc:creator>Chang Liu</dc:creator>
<dc:creator>Jiuhong Kang</dc:creator>
<dc:creator>Guixian Zhao</dc:creator>
<dc:creator>Zhiqiang Ye</dc:creator>
<dc:creator>Shichao Huang</dc:creator>
<dc:creator>Zhenxin Li</dc:creator>
<dc:creator>Zhiying Wu</dc:creator>
<dc:creator>Gang Pei</dc:creator>
<dc:identifier>doi:10.1038/ni.1798</dc:identifier>
<dc:source>Nature Immunology 10, 1252 (2009)</dc:source>
<dc:date>2009-10-18</dc:date>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:publicationDate>2009-10-18</prism:publicationDate>
<prism:doi>10.1038/ni.1798</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni.1798</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Article</prism:section>
<prism:startingPage>1252</prism:startingPage>
<prism:endingPage>1259</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/ni.1798</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/ni.1821">
<title>Requirement for the basic helix-loop-helix transcription factor Dec2 in initial TH2 lineage commitment</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/ywTQsF6zYV0/ni.1821</link>
<description>The molecular mediators responsible for directing T helper type 2 (TH2) differentiation remain incompletely defined. Dong and co-workers find that the transcription factor Dec2 promotes expression of the transcription factor JunB and is essential for the induction of TH2 responses.</description>
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>Requirement for the basic helix-loop-helix transcription factor Dec2 in initial TH2 lineage commitment</b>
</p>
<p>Nature Immunology 10, 1260 (2009). <a href="http://dx.doi.org/10.1038/ni.1821">doi:10.1038/ni.1821</a>
</p>
<p>Authors: Xuexian O Yang, Pornpimon Angkasekwinai, Jinfang Zhu, Juan Peng, Zhiduo Liu, Roza Nurieva, Xikui Liu, Yeonseok Chung, Seon Hee Chang, Bing Sun &amp; Chen Dong</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/ywTQsF6zYV0" height="1" width="1"/>]]></content:encoded>
<dc:title>Requirement for the basic helix-loop-helix transcription factor Dec2 in initial TH2 lineage commitment</dc:title>
<dc:creator>Xuexian O Yang</dc:creator>
<dc:creator>Pornpimon Angkasekwinai</dc:creator>
<dc:creator>Jinfang Zhu</dc:creator>
<dc:creator>Juan Peng</dc:creator>
<dc:creator>Zhiduo Liu</dc:creator>
<dc:creator>Roza Nurieva</dc:creator>
<dc:creator>Xikui Liu</dc:creator>
<dc:creator>Yeonseok Chung</dc:creator>
<dc:creator>Seon Hee Chang</dc:creator>
<dc:creator>Bing Sun</dc:creator>
<dc:creator>Chen Dong</dc:creator>
<dc:identifier>doi:10.1038/ni.1821</dc:identifier>
<dc:source>Nature Immunology 10, 1260 (2009)</dc:source>
<dc:date>2009-11-01</dc:date>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:doi>10.1038/ni.1821</prism:doi>
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<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Article</prism:section>
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<item rdf:about="http://dx.doi.org/10.1038/ni.1816">
<title>T cell–intrinsic role of Nod2 in promoting type 1 immunity to Toxoplasma gondii</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/p0A3bz5N280/ni.1816</link>
<description>Nod2 senses intracellular bacteria and is required for their eradication. Nuñez and co-workers now describe a T cell–intrinsic role for Nod2 in combating the intracellular parasite Toxoplasma gondii.</description>
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<p>
<b>T cell&#8211;intrinsic role of Nod2 in promoting type 1 immunity to Toxoplasma gondii</b>
</p>
<p>Nature Immunology 10, 1267 (2009). <a href="http://dx.doi.org/10.1038/ni.1816">doi:10.1038/ni.1816</a>
</p>
<p>Authors: Michael H Shaw, Thornik Reimer, Carmen S&#225;nchez-Valdepe&#241;as, Neil Warner, Yun-Gi Kim, Manuel Fresno &amp; Gabriel Nu&#241;ez</p>
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<dc:title>T cell–intrinsic role of Nod2 in promoting type 1 immunity to Toxoplasma gondii</dc:title>
<dc:creator>Michael H Shaw</dc:creator>
<dc:creator>Thornik Reimer</dc:creator>
<dc:creator>Carmen Sánchez-Valdepeñas</dc:creator>
<dc:creator>Neil Warner</dc:creator>
<dc:creator>Yun-Gi Kim</dc:creator>
<dc:creator>Manuel Fresno</dc:creator>
<dc:creator>Gabriel Nuñez</dc:creator>
<dc:identifier>doi:10.1038/ni.1816</dc:identifier>
<dc:source>Nature Immunology 10, 1267 (2009)</dc:source>
<dc:date>2009-11-01</dc:date>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:doi>10.1038/ni.1816</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni.1816</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Article</prism:section>
<prism:startingPage>1267</prism:startingPage>
<prism:endingPage>1274</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/ni.1816</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/ni.1793">
<title>Defective survival of naive CD8+ T lymphocytes in the absence of the β3 regulatory subunit of voltage-gated calcium channels</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/0KhcDanS7fQ/ni.1793</link>
<description>T cell activation triggers large calcium fluxes. Flavell and colleagues show tonic calcium signaling via Cav1.4-β3 channels are needed for the survival and homeostasis of naive CD8+ T cells.</description>
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>Defective survival of naive CD8+ T lymphocytes in the absence of the &#946;3 regulatory subunit of voltage-gated calcium channels</b>
</p>
<p>Nature Immunology 10, 1275 (2009). <a href="http://dx.doi.org/10.1038/ni.1793">doi:10.1038/ni.1793</a>
</p>
<p>Authors: Mithilesh K Jha, Abdallah Badou, Marcel Meissner, John E McRory, Marc Freichel, Veit Flockerzi &amp; Richard A Flavell</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/0KhcDanS7fQ" height="1" width="1"/>]]></content:encoded>
<dc:title>Defective survival of naive CD8+ T lymphocytes in the absence of the β3 regulatory subunit of voltage-gated calcium channels</dc:title>
<dc:creator>Mithilesh K Jha</dc:creator>
<dc:creator>Abdallah Badou</dc:creator>
<dc:creator>Marcel Meissner</dc:creator>
<dc:creator>John E McRory</dc:creator>
<dc:creator>Marc Freichel</dc:creator>
<dc:creator>Veit Flockerzi</dc:creator>
<dc:creator>Richard A Flavell</dc:creator>
<dc:identifier>doi:10.1038/ni.1793</dc:identifier>
<dc:source>Nature Immunology 10, 1275 (2009)</dc:source>
<dc:date>2009-10-18</dc:date>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:publicationDate>2009-10-18</prism:publicationDate>
<prism:doi>10.1038/ni.1793</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni.1793</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Article</prism:section>
<prism:startingPage>1275</prism:startingPage>
<prism:endingPage>1282</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/ni.1793</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/ni.1820">
<title>Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/W3Ck8yfeEUA/ni.1820</link>
<description>High-affinity and isotype-switched antibodies arise from germinal center reactions. Goodnow and colleagues identify the Rho guanine nucleotide–exchange factor DOCK8 as being essential for sustained B cell immune synapse formation in germinal centers and mature antibody responses.</description>
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production</b>
</p>
<p>Nature Immunology 10, 1283 (2009). <a href="http://dx.doi.org/10.1038/ni.1820">doi:10.1038/ni.1820</a>
</p>
<p>Authors: Katrina L Randall, Teresa Lambe, Andy Johnson, Bebhinn Treanor, Edyta Kucharska, Heather Domaschenz, Belinda Whittle, Lina E Tze, Anselm Enders, Tanya L Crockford, Tiphaine Bouriez-Jones, Duncan Alston, Jason G Cyster, Michael J Lenardo, Fabienne Mackay, Elissa K Deenick, Stuart G Tangye, Tyani D Chan, Tahra Camidge, Robert Brink, Carola G Vinuesa, Facundo D Batista, Richard J Cornall &amp; Christopher C Goodnow</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/W3Ck8yfeEUA" height="1" width="1"/>]]></content:encoded>
<dc:title>Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production</dc:title>
<dc:creator>Katrina L Randall</dc:creator>
<dc:creator>Teresa Lambe</dc:creator>
<dc:creator>Andy Johnson</dc:creator>
<dc:creator>Bebhinn Treanor</dc:creator>
<dc:creator>Edyta Kucharska</dc:creator>
<dc:creator>Heather Domaschenz</dc:creator>
<dc:creator>Belinda Whittle</dc:creator>
<dc:creator>Lina E Tze</dc:creator>
<dc:creator>Anselm Enders</dc:creator>
<dc:creator>Tanya L Crockford</dc:creator>
<dc:creator>Tiphaine Bouriez-Jones</dc:creator>
<dc:creator>Duncan Alston</dc:creator>
<dc:creator>Jason G Cyster</dc:creator>
<dc:creator>Michael J Lenardo</dc:creator>
<dc:creator>Fabienne Mackay</dc:creator>
<dc:creator>Elissa K Deenick</dc:creator>
<dc:creator>Stuart G Tangye</dc:creator>
<dc:creator>Tyani D Chan</dc:creator>
<dc:creator>Tahra Camidge</dc:creator>
<dc:creator>Robert Brink</dc:creator>
<dc:creator>Carola G Vinuesa</dc:creator>
<dc:creator>Facundo D Batista</dc:creator>
<dc:creator>Richard J Cornall</dc:creator>
<dc:creator>Christopher C Goodnow</dc:creator>
<dc:identifier>doi:10.1038/ni.1820</dc:identifier>
<dc:source>Nature Immunology 10, 1283 (2009)</dc:source>
<dc:date>2009-11-08</dc:date>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:publicationDate>2009-11-08</prism:publicationDate>
<prism:doi>10.1038/ni.1820</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni.1820</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Article</prism:section>
<prism:startingPage>1283</prism:startingPage>
<prism:endingPage>1291</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/ni.1814">
<title>Multiple layers of B cell memory with different effector functions</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/smDFYHV5tRU/ni.1814</link>
<description>Immunization elicits B cell memory and short- and long-term antibody-secreting plasma cells. Weill and colleagues show that long-term IgM+ and IgG+ memory B cells can persist in germinal centers and undergo different fates after antigenic rechallenge.</description>
<content:encoded><![CDATA[
<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>Multiple layers of B cell memory with different effector functions</b>
</p>
<p>Nature Immunology 10, 1292 (2009). <a href="http://dx.doi.org/10.1038/ni.1814">doi:10.1038/ni.1814</a>
</p>
<p>Authors: Ismail Dogan, Barbara Bertocci, Val&#233;rie Vilmont, Fr&#233;d&#233;ric Delbos, J&#233;rome M&#233;gret, S&#233;bastien Storck, Claude-Agn&#232;s Reynaud &amp; Jean-Claude Weill</p>
<img src="http://feeds.feedburner.com/~r/ni/rss/current/~4/smDFYHV5tRU" height="1" width="1"/>]]></content:encoded>
<dc:title>Multiple layers of B cell memory with different effector functions</dc:title>
<dc:creator>Ismail Dogan</dc:creator>
<dc:creator>Barbara Bertocci</dc:creator>
<dc:creator>Valérie Vilmont</dc:creator>
<dc:creator>Frédéric Delbos</dc:creator>
<dc:creator>Jérome Mégret</dc:creator>
<dc:creator>Sébastien Storck</dc:creator>
<dc:creator>Claude-Agnès Reynaud</dc:creator>
<dc:creator>Jean-Claude Weill</dc:creator>
<dc:identifier>doi:10.1038/ni.1814</dc:identifier>
<dc:source>Nature Immunology 10, 1292 (2009)</dc:source>
<dc:date>2009-10-25</dc:date>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:publicationDate>2009-10-25</prism:publicationDate>
<prism:doi>10.1038/ni.1814</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni.1814</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Article</prism:section>
<prism:startingPage>1292</prism:startingPage>
<prism:endingPage>1299</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/ni.1815">
<title>PCBP2 mediates degradation of the adaptor MAVS via the HECT ubiquitin ligase AIP4</title>
<link>http://feeds.nature.com/~r/ni/rss/current/~3/7KbaDeXuJgw/ni.1815</link>
<description>The mitochondrial adaptor MAVS is necessary for the transmission of RIG-I and Mda5 antiviral signals. Jiang and colleagues show that PCBP2 negatively regulates MAVS stability by recruiting the L48-ubiquitinating enzyme AIP4, thereby preventing excessive cytokine responses.</description>
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<div><a href="http://ad.doubleclick.net/adj/ni.nature.com/rss;sz=728x90"><img src="http://ad.doubleclick.net/ad/ni.nature.com/rss;sz=728x90" alt="Advertisement" style="border:0" /></a></div>
<p>
<b>PCBP2 mediates degradation of the adaptor MAVS via the HECT ubiquitin ligase AIP4</b>
</p>
<p>Nature Immunology 10, 1300 (2009). <a href="http://dx.doi.org/10.1038/ni.1815">doi:10.1038/ni.1815</a>
</p>
<p>Authors: Fuping You, Hui Sun, Xiang Zhou, Wenxiang Sun, Shimin Liang, Zhonghe Zhai &amp; Zhengfan Jiang</p>
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<dc:title>PCBP2 mediates degradation of the adaptor MAVS via the HECT ubiquitin ligase AIP4</dc:title>
<dc:creator>Fuping You</dc:creator>
<dc:creator>Hui Sun</dc:creator>
<dc:creator>Xiang Zhou</dc:creator>
<dc:creator>Wenxiang Sun</dc:creator>
<dc:creator>Shimin Liang</dc:creator>
<dc:creator>Zhonghe Zhai</dc:creator>
<dc:creator>Zhengfan Jiang</dc:creator>
<dc:identifier>doi:10.1038/ni.1815</dc:identifier>
<dc:source>Nature Immunology 10, 1300 (2009)</dc:source>
<dc:date>2009-11-01</dc:date>
<prism:publicationName>Nature Immunology</prism:publicationName>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:doi>10.1038/ni.1815</prism:doi>
<prism:url>http://dx.doi.org/10.1038/ni.1815</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
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<prism:startingPage>1300</prism:startingPage>
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