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TABLE OF CONTENTS
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May 2014 Volume 15, Issue 5 |
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| Commentary News and Views Research Highlights Review Articles
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Commentary | Top |
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Vaccines against tropical parasitic diseases: a persisting answer to a persisting problem pp403 - 405 David L Sacks doi:10.1038/ni.2853 Live whole-organism vaccines against Plasmodium falciparum malaria and cutaneous leishmaniasis remain the most uniformly effective vaccines against human parasitic diseases. These vaccines are discussed in terms of the requirement for persisting antigen to generate and maintain a protective response.
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News and Views | Top |
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Research Highlights | Top |
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Inflammasome 'prionization' | Human skin Treg cells | DC division of labor | Transcription concepts | Gut crosstalk | Facilitating Nod detection
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Review | Top |
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The enemy within: endogenous retroelements and autoimmune disease pp415 - 422 Hannah E Volkman and Daniel B Stetson doi:10.1038/ni.2872
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Articles | Top |
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Signaling by IL-6 promotes alternative activation of macrophages to limit endotoxemia and obesity-associated resistance to insulin pp423 - 430 Jan Mauer, Bhagirath Chaurasia, Julia Goldau, Merly C Vogt, Johan Ruud et al. doi:10.1038/ni.2865 The role of IL-6 in obesity-associated inflammation remains controversial. Bruening and colleagues identify signaling by IL-6 as an important determinant for the alternative activation of macrophages during inflammation.
See also: News and Views by Reilly & Saltiel
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The receptors CD96 and CD226 oppose each other in the regulation of natural killer cell functions pp431 - 438 Christopher J Chan, Ludovic Martinet, Susan Gilfillan, Fernando Souza-Fonseca-Guimaraes, Melvyn T Chow et al. doi:10.1038/ni.2850 The function of the lymphocyte-expressed receptor CD96 is almost entirely unknown. Smyth and colleagues demonstrate that it serves a key role in restraining activation of NK cells in part by competing with the activating receptor CD226 (DNAM-1).
See also: News and Views by Bernhardt
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CD4+ T cell lineage integrity is controlled by the histone deacetylases HDAC1 and HDAC2 pp439 - 448 Nicole Boucheron, Roland Tschismarov, Lisa Goeschl, Mirjam A Moser, Sabine Lagger et al. doi:10.1038/ni.2864 Histone deacetylases (HDACs) are crucial regulators of cell identity. Ellmeier and colleagues show that HDAC1 and HDAC2 maintain CD4+ T cell lineage integrity by repressing Runx-CBFβ complexes in TH1 cells but not in TH2 cells.
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The adaptor TRAF5 limits the differentiation of inflammatory CD4+ T cells by antagonizing signaling via the receptor for IL-6 pp449 - 456 Hiroyuki Nagashima, Yuko Okuyama, Atsuko Asao, Takeshi Kawabe, Satoshi Yamaki et al. doi:10.1038/ni.2863 Adaptors of the TRAF family are tumor-necrosis factor receptor-associated factors. So and colleagues show that TRAF5 negative regulates the IL-6 receptor signaling pathway, which limits the induction of proinflammatory CD4+ T cells.
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The AGC kinase SGK1 regulates TH1 and TH2 differentiation downstream of the mTORC2 complex pp457 - 464 Emily B Heikamp, Chirag H Patel, Sam Collins, Adam Waickman, Min-Hee Oh et al. doi:10.1038/ni.2867 The kinase SGK1 is a downstream target of mTORC2 signaling. Powell and colleagues show that SGK1 regulates TH2 polarization by increasing the stability of the transcription factor JunB and antagonizing IFN-γ expression.
See also: News and Views by Norton & Screaton
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Protein kinase C-η controls CTLA-4-mediated regulatory T cell function pp465 - 472 Kok-Fai Kong, Guo Fu, Yaoyang Zhang, Tadashi Yokosuka, Javier Casas et al. doi:10.1038/ni.2866 Signaling events at the Treg cell immune synapse remain unknown. Altman and colleagues show that a CTLA-4-PKC-η signaling axis is required for contact-dependent suppression by Treg cells.
See also: News and Views by Wulfing et al.
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Costimulation via the tumor-necrosis factor receptor superfamily couples TCR signal strength to the thymic differentiation of regulatory T cells pp473 - 481 Shawn A Mahmud, Luke S Manlove, Heather M Schmitz, Yan Xing, Yanyan Wang et al. doi:10.1038/ni.2849 The precise mechanisms of the thymic development Treg cells are still being determined. Farrar and colleagues demonstrate that signals from a triumvirate of members of the tumor-necrosis factor receptor superfamily are critical for Treg cell development in the thymus.
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