Friday, April 18, 2014

Nature Immunology Contents: May 2014 Volume 15 pp 403 - 481

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Nature Immunology

TABLE OF CONTENTS

May 2014 Volume 15, Issue 5

Commentary
News and Views
Research Highlights
Review
Articles

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Commentary

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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.

News and Views

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TACTILE becomes tangible: CD96 discloses its inhibitory peculiarities   pp406 - 408
Günter Bernhardt
doi:10.1038/ni.2855
The receptor CD96 inhibits cytokine production by natural killer cells in mice and antagonizes activation mediated by the receptor CD226.

See also: Article by Chan et al.

New inhibitory signaling by CTLA-4   pp408 - 409
Christoph Wülfing, Helen M Tunbridge and David C Wraith
doi:10.1038/ni.2870
CTLA-4 is a potent inhibitor of T cell population expansion. The PIX-GIT2-PAK2 complex is recruited to the cytoplasmic domain of CTLA-4 via the kinase PKC-η, which suggests a previously unrecognized aspect of signal transduction via CTLA-4 in immunoregulation.

See also: Article by Kong et al.

Countering inflammatory signals in obesity   pp410 - 411
Shannon M Reilly and Alan R Saltiel
doi:10.1038/ni.2874
Although it is generally considered a proinflammatory cytokine, interleukin 6 (IL-6) has anti-inflammatory effects in macrophages by sensitizing them to IL-4 through upregulation of the IL-4 receptor.

See also: Article by Mauer et al.

SGK1: master and commander of the fate of helper T cells   pp411 - 413
Matthew Norton and Robert A Screaton
doi:10.1038/ni.2875
Cytokines and other environmental cues influence polarization of CD4+ helper T cells, but the signaling pathways that are involved are less clear. Recent findings show that signaling via an mTORC2-SGK1 kinase axis regulates TH1-TH2 cell-fate polarization.

See also: Article by Heikamp et al.

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Research Highlights

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Inflammasome 'prionization' | Human skin Treg cells | DC division of labor | Transcription concepts | Gut crosstalk | Facilitating Nod detection


Review

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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

Articles

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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

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

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.

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.

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

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.

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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