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<pubDate>Sun, 27 Jul 2008 06:06:25 BST</pubDate>


	<title>CiteULike: AlfonsoVicenteSuarez's Sher</title>
	<description>CiteULike: AlfonsoVicenteSuarez's Sher</description>


	<link>http://www.citeulike.org/user/AlfonsoVicenteSuarez/author/Sher</link>
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<item rdf:about="http://www.citeulike.org/user/AlfonsoVicenteSuarez/article/1402632">
    <title>Conventional T-bet+Foxp3- Th1 cells are the major source of host-protective regulatory IL-10 during intracellular protozoan infection</title>
    <link>http://www.citeulike.org/user/AlfonsoVicenteSuarez/article/1402632</link>
    <description>&lt;i&gt;J. Exp. Med., Vol. 204, No. 2. (19 February 2007), pp. 273-283.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Although interferon gamma (IFN-gamma) secretion is essential for control of most intracellular pathogens, host survival often also depends on the expression of interleukin 10 (IL-10), a cytokine known to counteract IFN-gamma effector functions. We analyzed the source of regulatory IL-10 in mice infected with the protozoan parasite Toxoplasma gondii. Unexpectedly, IFN-gamma-secreting T-bet+Foxp3- T helper type 1 (Th1) cells were found to be the major producers of IL-10 in these animals. Further analysis revealed that the same IL-10+IFN-gammagamma population displayed potent effector function against the parasite while, paradoxically, also inducing profound suppression of IL-12 production by antigen-presenting cells. Although at any given time point only a fraction of the cells appeared to simultaneously produce IL-10 and IFN-gamma, IL-10 production could be stimulated in IL-10-IFN-gamma+ cells by further activation in vitro. In addition, experiments with T. gondii-specific IL-10+IFN-gamma+ CD4 clones revealed that although IFN-gamma expression is imprinted and triggered with similar kinetics regardless of the state of Th1 cell activation, IL-10 secretion is induced more rapidly from recently activated than from resting cells. These findings indicate that IL-10 production by CD4+ T lymphocytes need not involve a distinct regulatory Th cell subset but can be generated in Th1 cells as part of the effector response to intracellular pathogens. 10.1084/jem.20062175</description>
    <dc:title>Conventional T-bet+Foxp3- Th1 cells are the major source of host-protective regulatory IL-10 during intracellular protozoan infection</dc:title>

    <dc:creator>Dragana Jankovic</dc:creator>
    <dc:creator>Marika Kullberg</dc:creator>
    <dc:creator>Carl Feng</dc:creator>
    <dc:creator>Romina Goldszmid</dc:creator>
    <dc:creator>Carmen Collazo</dc:creator>
    <dc:creator>Mark Wilson</dc:creator>
    <dc:creator>Thomas Wynn</dc:creator>
    <dc:creator>Masahito Kamanaka</dc:creator>
    <dc:creator>Richard Flavell</dc:creator>
    <dc:creator>Alan Sher</dc:creator>
    <dc:identifier>doi:10.1084/jem.20062175</dc:identifier>
    <dc:source>J. Exp. Med., Vol. 204, No. 2. (19 February 2007), pp. 273-283.</dc:source>
    <dc:date>2007-06-21T15:11:34-00:00</dc:date>
    <prism:publicationYear>2007</prism:publicationYear>
    <prism:publicationName>J. Exp. Med.</prism:publicationName>
    <prism:volume>204</prism:volume>
    <prism:number>2</prism:number>
    <prism:startingPage>273</prism:startingPage>
    <prism:endingPage>283</prism:endingPage>
    <prism:category>il-10-tcells</prism:category>
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<item rdf:about="http://www.citeulike.org/user/AlfonsoVicenteSuarez/article/1119389">
    <title>Cooperation of Toll-like receptor signals in innate immune defence</title>
    <link>http://www.citeulike.org/user/AlfonsoVicenteSuarez/article/1119389</link>
    <description>&lt;i&gt;Nature Reviews Immunology, Vol. 7, No. 3., pp. 179-190.&lt;/i&gt;</description>
    <dc:title>Cooperation of Toll-like receptor signals in innate immune defence</dc:title>

    <dc:creator>Giorgio Trinchieri</dc:creator>
    <dc:creator>Alan Sher</dc:creator>
    <dc:identifier>doi:10.1038/nri2038</dc:identifier>
    <dc:source>Nature Reviews Immunology, Vol. 7, No. 3., pp. 179-190.</dc:source>
    <dc:date>2007-02-23T22:17:07-00:00</dc:date>
    <prism:publicationName>Nature Reviews Immunology</prism:publicationName>
    <prism:issn>1474-1733</prism:issn>
    <prism:volume>7</prism:volume>
    <prism:number>3</prism:number>
    <prism:startingPage>179</prism:startingPage>
    <prism:endingPage>190</prism:endingPage>
    <prism:publisher>Nature Publishing Group</prism:publisher>
    <prism:category>tlr-signaling</prism:category>
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