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<title>Nature Reviews Immunology</title>
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<title>The functional plasticity of T cell subsets</title>
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<description>In 1986, Robert Coffman and Timothy Mossman first described the division of CD4+ T cells into functional subsets, termed T helper 1 (TH1) and TH2, based on cytokine production, and in doing so unwittingly opened a Pandora's box of </description>
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<p>
<b>The functional plasticity of T cell subsets</b>
</p>
<p>Nature Reviews Immunology 9, 811 (2009). <a href="http://dx.doi.org/10.1038/nri2654">doi:10.1038/nri2654</a>
</p>
<p>Authors: Jeffrey A. Bluestone, Charles R. Mackay, John J. O'Shea &amp; Brigitta Stockinger</p>
<p>In 1986, Robert Coffman and Timothy Mossman first described the division of CD4+ T cells into functional subsets, termed T helper 1 (TH1) and TH2, based on cytokine production, and in doing so unwittingly opened a Pandora's box of </p>
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<dc:title>The functional plasticity of T cell subsets</dc:title>
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<title>Analysing immune cell migration</title>
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<description>The visualization of the dynamic behaviour of and interactions between immune cells using time-lapse video microscopy has an important role in modern immunology. To draw robust conclusions, quantification of such cell migration is required. However, imaging experiments are associated with various artefacts that can affect </description>
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<p>
<b>Analysing immune cell migration</b>
</p>
<p>Nature Reviews Immunology 9, 789 (2009). <a href="http://dx.doi.org/10.1038/nri2638">doi:10.1038/nri2638</a>
</p>
<p>Authors: Joost B. Beltman, Athanasius F. M. Mar&#233;e &amp; Rob J. de Boer</p>
<p>The visualization of the dynamic behaviour of and interactions between immune cells using time-lapse video microscopy has an important role in modern immunology. To draw robust conclusions, quantification of such cell migration is required. However, imaging experiments are associated with various artefacts that can affect </p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/x9bX3hNqY9g" height="1" width="1"/>]]></content:encoded>
<dc:title>Analysing immune cell migration</dc:title>
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<title>Mast cells: Delivery of cytokine packages to the lymph nodes</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/FDSVoVe_0pk/nri2658</link>
<description>During infection, draining lymph nodes undergo growth and remodelling to facilitate the interactions between immune cells. These morphological changes in the lymphoid tissue are thought to be induced by cytokines released at the site of immune challenge; however, it is not known how the cytokines </description>
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<p>
<b>Mast cells: Delivery of cytokine packages to the lymph nodes</b>
</p>
<p>Nature Reviews Immunology 9, 752 (2009). <a href="http://dx.doi.org/10.1038/nri2658">doi:10.1038/nri2658</a>
</p>
<p>Author: Gemma Ryan</p>
<p>During infection, draining lymph nodes undergo growth and remodelling to facilitate the interactions between immune cells. These morphological changes in the lymphoid tissue are thought to be induced by cytokines released at the site of immune challenge; however, it is not known how the cytokines </p>
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<dc:title>Mast cells: Delivery of cytokine packages to the lymph nodes</dc:title>
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<dc:source>Nature Reviews Immunology 9, 752 (2009)</dc:source>
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<title>Immune regulation: TReg cells offer a bespoke service</title>
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<description>Regulatory T (TReg) cells provide tailor-made control of the immune response, according to new research by Alexander Rudensky and colleagues. Effector CD4+ T cells differentiate into functionally distinct T helper (TH) cell populations — TH1, TH</description>
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<p>
<b>Immune regulation: TReg cells offer a bespoke service</b>
</p>
<p>Nature Reviews Immunology 9, 754 (2009). <a href="http://dx.doi.org/10.1038/nri2659">doi:10.1038/nri2659</a>
</p>
<p>Author: Kirsty Minton</p>
<p>Regulatory T (TReg) cells provide tailor-made control of the immune response, according to new research by Alexander Rudensky and colleagues. Effector CD4+ T cells differentiate into functionally distinct T helper (TH) cell populations &#8212; TH1, TH</p>
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<dc:title>Immune regulation: TReg cells offer a bespoke service</dc:title>
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<title>T cell development: Seeing self in a positive light</title>
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<description>Weak interactions between T cell receptors (TCRs) and self-peptide–MHC complexes induce positive selection of double-positive thymocytes in the thymus. Naturally occurring self peptides involved in positive selection have been identified only for CD8+ T cells. Now, two papers published in Nature Immunology</description>
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<p>
<b>T cell development: Seeing self in a positive light</b>
</p>
<p>Nature Reviews Immunology 9, 751 (2009). <a href="http://dx.doi.org/10.1038/nri2661">doi:10.1038/nri2661</a>
</p>
<p>Author: Olive Leavy</p>
<p>Weak interactions between T cell receptors (TCRs) and self-peptide&#8211;MHC complexes induce positive selection of double-positive thymocytes in the thymus. Naturally occurring self peptides involved in positive selection have been identified only for CD8+ T cells. Now, two papers published in Nature Immunology</p>
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<dc:title>T cell development: Seeing self in a positive light</dc:title>
<dc:creator>Olive Leavy</dc:creator>
<dc:identifier>doi:10.1038/nri2661</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 751 (2009)</dc:source>
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<title>New insights into the differentiation and function of T follicular helper cells</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/_yEnqDpFbSw/nri2644</link>
<description>The seminal studies characterizing T follicular helper (TFH) cells described a non-polarized CD4+ T cell population with a unique ability to home to B cell follicles and to induce antibody production by B cells. In the past few years, the study </description>
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<p>
<b>New insights into the differentiation and function of T follicular helper cells</b>
</p>
<p>Nature Reviews Immunology 9, 757 (2009). <a href="http://dx.doi.org/10.1038/nri2644">doi:10.1038/nri2644</a>
</p>
<p>Author: Cecile King</p>
<p>The seminal studies characterizing T follicular helper (TFH) cells described a non-polarized CD4+ T cell population with a unique ability to home to B cell follicles and to induce antibody production by B cells. In the past few years, the study </p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/_yEnqDpFbSw" height="1" width="1"/>]]></content:encoded>
<dc:title>New insights into the differentiation and function of T follicular helper cells</dc:title>
<dc:creator>Cecile King</dc:creator>
<dc:identifier>doi:10.1038/nri2644</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 757 (2009)</dc:source>
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<title>Intestinal mucosal barrier function in health and disease</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/GNbC-EwfiKk/nri2653</link>
<description>Mucosal surfaces are lined by epithelial cells. These cells establish a barrier between sometimes hostile external environments and the internal milieu. However, mucosae are also responsible for nutrient absorption and waste secretion, which require a selectively permeable barrier. These functions place the mucosal epithelium at </description>
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<p>
<b>Intestinal mucosal barrier function in health and disease</b>
</p>
<p>Nature Reviews Immunology 9, 799 (2009). <a href="http://dx.doi.org/10.1038/nri2653">doi:10.1038/nri2653</a>
</p>
<p>Author: Jerrold R. Turner</p>
<p>Mucosal surfaces are lined by epithelial cells. These cells establish a barrier between sometimes hostile external environments and the internal milieu. However, mucosae are also responsible for nutrient absorption and waste secretion, which require a selectively permeable barrier. These functions place the mucosal epithelium at </p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/GNbC-EwfiKk" height="1" width="1"/>]]></content:encoded>
<dc:title>Intestinal mucosal barrier function in health and disease</dc:title>
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<dc:identifier>doi:10.1038/nri2653</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 799 (2009)</dc:source>
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<title>Regulation of tissue homeostasis by NF-κB signalling: implications for inflammatory diseases</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/9dxtlEAZlPw/nri2655</link>
<description>The nuclear factor-κB (NF-κB) signalling pathway regulates immune responses and is implicated in the pathogenesis of many inflammatory diseases. Given the well established pro-inflammatory functions of NF-κB, inhibition of this pathway would be expected to have anti-inflammatory effects. However, recent studies in mouse models have </description>
<content:encoded><![CDATA[

<p>
<b>Regulation of tissue homeostasis by NF-&#954;B signalling: implications for inflammatory diseases</b>
</p>
<p>Nature Reviews Immunology 9, 778 (2009). <a href="http://dx.doi.org/10.1038/nri2655">doi:10.1038/nri2655</a>
</p>
<p>Author: Manolis Pasparakis</p>
<p>The nuclear factor-&#954;B (NF-&#954;B) signalling pathway regulates immune responses and is implicated in the pathogenesis of many inflammatory diseases. Given the well established pro-inflammatory functions of NF-&#954;B, inhibition of this pathway would be expected to have anti-inflammatory effects. However, recent studies in mouse models have </p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/9dxtlEAZlPw" height="1" width="1"/>]]></content:encoded>
<dc:title>Regulation of tissue homeostasis by NF-κB signalling: implications for inflammatory diseases</dc:title>
<dc:creator>Manolis Pasparakis</dc:creator>
<dc:identifier>doi:10.1038/nri2655</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 778 (2009)</dc:source>
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<title>The follicular versus marginal zone B lymphocyte cell fate decision</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/VNCMDkdWNwY/nri2656</link>
<description>Bone marrow-derived B cells make an important cell fate choice to develop into either follicular B cells or marginal zone B cells in the spleen, which depends on signalling through the B cell receptor, Notch2, the receptor for B cell-activating factor and the canonical nuclear </description>
<content:encoded><![CDATA[

<p>
<b>The follicular versus marginal zone B lymphocyte cell fate decision</b>
</p>
<p>Nature Reviews Immunology 9, 767 (2009). <a href="http://dx.doi.org/10.1038/nri2656">doi:10.1038/nri2656</a>
</p>
<p>Authors: Shiv Pillai &amp; Annaiah Cariappa</p>
<p>Bone marrow-derived B cells make an important cell fate choice to develop into either follicular B cells or marginal zone B cells in the spleen, which depends on signalling through the B cell receptor, Notch2, the receptor for B cell-activating factor and the canonical nuclear </p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/VNCMDkdWNwY" height="1" width="1"/>]]></content:encoded>
<dc:title>The follicular versus marginal zone B lymphocyte cell fate decision</dc:title>
<dc:creator>Shiv Pillai</dc:creator>
<dc:creator>Annaiah Cariappa</dc:creator>
<dc:identifier>doi:10.1038/nri2656</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 767 (2009)</dc:source>
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<title>Dendritic cells: Division of DC labour in the gut</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/r3gYegHGmmo/nri2662</link>
<description>As far as the immune system is concerned, the gut is full of bacterial friends and foes: commensal microorganisms must be tolerated, whereas pathogens must be expelled. At the front line, maintaining this balance, are dendritic cells (DCs). Two groups reporting in Immunity have </description>
<content:encoded><![CDATA[

<p>
<b>Dendritic cells: Division of DC labour in the gut</b>
</p>
<p>Nature Reviews Immunology 9, 755 (2009). <a href="http://dx.doi.org/10.1038/nri2662">doi:10.1038/nri2662</a>
</p>
<p>Author: Ruth Williams</p>
<p>As far as the immune system is concerned, the gut is full of bacterial friends and foes: commensal microorganisms must be tolerated, whereas pathogens must be expelled. At the front line, maintaining this balance, are dendritic cells (DCs). Two groups reporting in Immunity have </p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/r3gYegHGmmo" height="1" width="1"/>]]></content:encoded>
<dc:title>Dendritic cells: Division of DC labour in the gut</dc:title>
<dc:creator>Ruth Williams</dc:creator>
<dc:identifier>doi:10.1038/nri2662</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 755 (2009)</dc:source>
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<title>T Cells: Crawling into the brain</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/viH7pXpKo8c/nri2663</link>
<description>A study involving real-time imaging of effector T cells provides new insight into how autoreactive T cells interact with cerebral structures and access the central nervous system (CNS) to cause autoimmune disease.Flügel and colleagues induced experimental autoimmune encephalomyelitis in rats with intravenous injection of </description>
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<p>
<b>T Cells: Crawling into the brain</b>
</p>
<p>Nature Reviews Immunology 9, 752 (2009). <a href="http://dx.doi.org/10.1038/nri2663">doi:10.1038/nri2663</a>
</p>
<p>Author: Lucy Bird</p>
<p>A study involving real-time imaging of effector T cells provides new insight into how autoreactive T cells interact with cerebral structures and access the central nervous system (CNS) to cause autoimmune disease.Fl&#252;gel and colleagues induced experimental autoimmune encephalomyelitis in rats with intravenous injection of </p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/viH7pXpKo8c" height="1" width="1"/>]]></content:encoded>
<dc:title>T Cells: Crawling into the brain</dc:title>
<dc:creator>Lucy Bird</dc:creator>
<dc:identifier>doi:10.1038/nri2663</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 752 (2009)</dc:source>
<prism:publicationName>Nature Reviews Immunology</prism:publicationName>
<prism:doi>10.1038/nri2663</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nri2663</prism:url>
<prism:volume>9</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>752</prism:startingPage>
<prism:endingPage>753</prism:endingPage>
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<title>From the editors</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/8LgbOlQu_Wo/nri2664</link>
<description>Immunologists have become more adept at distinguishing different types of B and T cell, leading to new questions about the functions and differentiation pathways of these cells. Understanding how these phenotypes arise and interact holds the promise of more effective immunotherapies and vaccines with fewer </description>
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<p>
<b>From the editors</b>
</p>
<p>Nature Reviews Immunology 9, 749 (2009). <a href="http://dx.doi.org/10.1038/nri2664">doi:10.1038/nri2664</a>
</p>
<p>Immunologists have become more adept at distinguishing different types of B and T cell, leading to new questions about the functions and differentiation pathways of these cells. Understanding how these phenotypes arise and interact holds the promise of more effective immunotherapies and vaccines with fewer </p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/8LgbOlQu_Wo" height="1" width="1"/>]]></content:encoded>
<dc:title>From the editors</dc:title>
<dc:identifier>doi:10.1038/nri2664</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 749 (2009)</dc:source>
<prism:publicationName>Nature Reviews Immunology</prism:publicationName>
<prism:doi>10.1038/nri2664</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nri2664</prism:url>
<prism:volume>9</prism:volume>
<prism:number>11</prism:number>
<prism:section>From The Editors</prism:section>
<prism:startingPage>749</prism:startingPage>
<prism:endingPage>749</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nri2664</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nri2665">
<title>Immunotherapy: CpG–siRNA deals double blow to tumours</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/Y4h8fYfWFyQ/nri2665</link>
<description>Tumours can avert an immune response and boost their own growth by inducing the expression of immunosuppressive, angiogenic and growth factors by neighbouring cells. Reporting in Nature Biotechnology, Kortylewski and colleagues now present a new strategy to alter the balance in the tumour microenvironment </description>
<content:encoded><![CDATA[

<p>
<b>Immunotherapy: CpG&#8211;siRNA deals double blow to tumours</b>
</p>
<p>Nature Reviews Immunology 9, 753 (2009). <a href="http://dx.doi.org/10.1038/nri2665">doi:10.1038/nri2665</a>
</p>
<p>Author: Alexandra Flemming</p>
<p>Tumours can avert an immune response and boost their own growth by inducing the expression of immunosuppressive, angiogenic and growth factors by neighbouring cells. Reporting in Nature Biotechnology, Kortylewski and colleagues now present a new strategy to alter the balance in the tumour microenvironment </p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/Y4h8fYfWFyQ" height="1" width="1"/>]]></content:encoded>
<dc:title>Immunotherapy: CpG–siRNA deals double blow to tumours</dc:title>
<dc:creator>Alexandra Flemming</dc:creator>
<dc:identifier>doi:10.1038/nri2665</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 753 (2009)</dc:source>
<prism:publicationName>Nature Reviews Immunology</prism:publicationName>
<prism:doi>10.1038/nri2665</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nri2665</prism:url>
<prism:volume>9</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>753</prism:startingPage>
<prism:endingPage>753</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nri2665</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nri2666">
<title>In Brief</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/jEtLGHCK86w/nri2666</link>
<description>Innate immunity</description>
<content:encoded><![CDATA[

<p>
<b>In Brief</b>
</p>
<p>Nature Reviews Immunology 9, 752 (2009). <a href="http://dx.doi.org/10.1038/nri2666">doi:10.1038/nri2666</a>
</p>
<p>Innate immunity</p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/jEtLGHCK86w" height="1" width="1"/>]]></content:encoded>
<dc:title>In Brief</dc:title>
<dc:identifier>doi:10.1038/nri2666</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 752 (2009)</dc:source>
<prism:publicationName>Nature Reviews Immunology</prism:publicationName>
<prism:doi>10.1038/nri2666</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nri2666</prism:url>
<prism:volume>9</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>752</prism:startingPage>
<prism:endingPage>752</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nri2667">
<title>In Brief</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/KBQ0mSAU-Os/nri2667</link>
<description>Immune tolerance</description>
<content:encoded><![CDATA[

<p>
<b>In Brief</b>
</p>
<p>Nature Reviews Immunology 9, 754 (2009). <a href="http://dx.doi.org/10.1038/nri2667">doi:10.1038/nri2667</a>
</p>
<p>Immune tolerance</p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/KBQ0mSAU-Os" height="1" width="1"/>]]></content:encoded>
<dc:title>In Brief</dc:title>
<dc:identifier>doi:10.1038/nri2667</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 754 (2009)</dc:source>
<prism:publicationName>Nature Reviews Immunology</prism:publicationName>
<prism:doi>10.1038/nri2667</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nri2667</prism:url>
<prism:volume>9</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>754</prism:startingPage>
<prism:endingPage>754</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nri2667</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nri2668">
<title>HIV vaccine results controversy</title>
<link>http://feeds.nature.com/~r/nri/rss/current/~3/tAXNNpH8vSk/nri2668</link>
<description>An announcement, by researchers from the US Army and Thailand, at a recent press conference of the first positive results from an HIV vaccine trial was met with media fanfare but cautious optimism from scientists.The RV 144 vaccine, which combines two vaccines (ALVAC and </description>
<content:encoded><![CDATA[

<p>
<b>HIV vaccine results controversy</b>
</p>
<p>Nature Reviews Immunology 9, 755 (2009). <a href="http://dx.doi.org/10.1038/nri2668">doi:10.1038/nri2668</a>
</p>
<p>Author: Olive Leavy</p>
<p>An announcement, by researchers from the US Army and Thailand, at a recent press conference of the first positive results from an HIV vaccine trial was met with media fanfare but cautious optimism from scientists.The RV 144 vaccine, which combines two vaccines (ALVAC and </p>
<img src="http://feeds.feedburner.com/~r/nri/rss/current/~4/tAXNNpH8vSk" height="1" width="1"/>]]></content:encoded>
<dc:title>HIV vaccine results controversy</dc:title>
<dc:creator>Olive Leavy</dc:creator>
<dc:identifier>doi:10.1038/nri2668</dc:identifier>
<dc:source>Nature Reviews Immunology 9, 755 (2009)</dc:source>
<prism:publicationName>Nature Reviews Immunology</prism:publicationName>
<prism:doi>10.1038/nri2668</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nri2668</prism:url>
<prism:volume>9</prism:volume>
<prism:number>11</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>755</prism:startingPage>
<prism:endingPage>755</prism:endingPage>
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