Friday, August 22, 2014

Nature Reviews Immunology Contents September 2014 Volume 14 Number 9 pp 579-646

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Nature Reviews Immunology

 
TABLE OF CONTENTS
 
September 2014 Volume 14 Number 9
Nature Reviews Immunology cover
Impact Factor 33.836 *
In this issue
Research Highlights
Reviews
Analysis
Perspectives

Also this month
 Featured article:
The IL-23–IL-17 immune axis: from mechanisms to therapeutic testing
Sarah L. Gaffen, Renu Jain, Abhishek V. Garg & Daniel J. Cua


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RESEARCH HIGHLIGHTS
Top

Regulatory T cells: Alarmin(g) control
p579 | doi:10.1038/nri3733
In response to intestinal tissue damage, the alarmin interleukin-33 enhances local regulatory T cell responses.
PDF


Inflammasomes: Ubiquitin lines up for inflammasome activity
p580 | doi:10.1038/nri3730
Linear ubiquitylation of the adaptor protein ASC regulates interleukin-1β production by the NLRP3 inflammasome.
PDF


Mucosal immunology: Eosinophils get the party started
p580 | doi:10.1038/nri3731
Eosinophils initiate T helper 2 cell responses in the small intestine by promoting dendritic cell activation.
PDF


Regulatory T cells: A message of peace
p581 | doi:10.1038/nri3729
Regulatory T cells suppress effector T cells by releasing exosomes that contain microRNAs.
PDF


Mucosal immunology: Killing time in the lungs
p582 | doi:10.1038/nri3732
Pulmonary epithelial cells drive rhythmic neutrophil recruitment by secreting chemokines in a clock-dependent manner.
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Inflammasomes: New LPS receptors discovered
p582 | doi:10.1038/nri3736
A new study identifies inflammatory caspases as the cytoplasmic LPS receptors that trigger non-canonical inflammasome activation.
PDF


Pattern recognition receptors: Curbing gut inflammation
p583 | doi:10.1038/nri3735
NOD2 restricts small intestinal inflammation by controlling the overgrowth of commensal bacteria.
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Immunology
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REVIEWS
Top
The IL-23–IL-17 immune axis: from mechanisms to therapeutic testing
Sarah L. Gaffen, Renu Jain, Abhishek V. Garg & Daniel J. Cua
p585 | doi:10.1038/nri3707
T helper 17 (TH17) cells promote protective immune responses against infection, particularly at barrier sites, but they can also have pathogenic roles in inflammatory diseases. In this Review, the authors describe the factors that control the development and maintenance of TH17 cells, and discuss their diverse functions in both health and disease.
Abstract | Full Text | PDF | Supplementary information

A long-awaited merger of the pathways mediating host defence and programmed cell death
J. Magarian Blander
p601 | doi:10.1038/nri3720
There is a growing appreciation of how the host inflammatory response is intricately entwined with the various forms of programmed cell death. This Review discusses the signalling mechanisms that link these processes, with a particular focus on how the key mediators of cell death, such as the caspases, are integrated into innate signalling modules.
Abstract | Full Text | PDF | Supplementary information

 
ANALYSIS
Top
Phenotypic models of T cell activation
Melissa Lever, Philip K. Maini, P. Anton van der Merwe & Omer Dushek
p619 | doi:10.1038/nri3728
There is currently no single model that fits the wealth of experimental data that relate T cell activation to T cell receptor-peptide-MHC binding parameters. Here, the authors analyse and reformulate the published models, and suggest that a kinetic proofreading model that involves limited T cell receptor signalling provides the best fit.
Abstract | Full Text | PDF | Supplementary information
 
PERSPECTIVES
Top
OPINION
Interactions between innate and adaptive lymphocytes
Georg Gasteiger & Alexander Y. Rudensky
p631 | doi:10.1038/nri3726
Recent evidence indicates that adaptive T cell-mediated immune responses can regulate innate lymphocytes (natural killer cells and innate lymphoid cells) in an interleukin-2-dependent manner. The authors propose a model in which adaptive T cells function as peripheral antigen-specific sensors that recruit and activate innate lymphocytes to amplify and coordinate local immune responses.
Abstract | Full Text | PDF

OPINION
Natural killer T cells: drivers or passengers in preventing human disease?
Stuart P. Berzins & David S. Ritchie
p640 | doi:10.1038/nri3725
Natural killer T (NKT) cell defects have been implicated in several diseases such as autoimmunity, asthma and cancer, but will targeting them really be of clinical benefit? Here, the authors investigate this question and conclude that more careful studies are needed before the true clinical potential of NKT cell-targeted therapies can be determined.
Abstract | Full Text | PDF

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