Monday, November 25, 2013

Nature Reviews Immunology Contents December 2013 Volume 13 Number 12 pp 839-902

Nature Reviews Immunology


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Mechanisms underlying CD4+ Treg immune regulation in the adult: from experiments to models (open access)

In this mini-review published in Frontiers in Immunology Marta Caridade, Luis Graca and Ruy M. Ribeiro discuss some of the known and proposed mechanisms by which Tregs exert their influence in the context of immune regulation, and the contribution of mathematical modeling for these mechanistic studies.
 
TABLE OF CONTENTS
 
December 2013 Volume 13 Number 12

Nature Reviews Immunology cover
Impact Factor 33.129 *
In this issue
Comment
Research Highlights
Reviews
Correspondence

Also this month
 Featured article:
Sepsis-induced immunosuppression: from cellular dysfunctions to immunotherapy
Richard S. Hotchkiss, Guillaume Monneret & Didier Payen




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Comment: Nobel Prize discovery paves the way for immunological traffic
Jennifer L. Stow
p839 | doi:10.1038/nri3564
The 2013 Nobel Prize for Physiology or Medicine recognizes James Rothman, Randy Schekman and Thomas Sudhof, whose work over several decades has characterized key components and mechanisms of the trafficking machinery in eukaryotic cells. Reflecting on these Nobel Prize-winning discoveries raises some important and exciting prospects for immunologists.
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RESEARCH HIGHLIGHTS

Top

Antibodies: Taking the sting out
p843 | doi:10.1038/nri3568
IgE responses to venom protect animals against potentially lethal subsequent exposures to the venom.
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T cell responses: A dendritic cell designed for two
p844 | doi:10.1038/nri3560
A novel population of CD301b+ dendritic cells potentiates TH2-type immune responses.
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Natural killer cells: A virtual pick and mix
p844 | doi:10.1038/nri3566
Genes and environment contribute to a vast diversity of human NK cell phenotypes.
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Immunometabolism: Mef2 in sickness and in health
p845 | doi:10.1038/nri3563
Phosphorylation of Mef2 controls immune versus metabolic gene expression in infected Drosophila melanogaster.
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Tumour immunology: Dealing with regulators
p846 | doi:10.1038/nri3569
CCR4-specific antibodies deplete regulatory T cells and boost antitumour responses in humans.
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HIV: Advancing the antibody approach
p846 | doi:10.1038/nri3573
Antibodies come to the fore in therapeutic and prophylactic approaches to suppress SHIV in macaques.
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Infectious disease: Hushing mTOR boosts immunity to pathogens
p847 | doi:10.1038/nri3562
Suppression of mTOR signalling can promote immunity to intracellular pathogens.
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T cells: Adenosine maintains the numbers
p848 | doi:10.1038/nri3571
Adenosine regulates thymocyte development and maintains peripheral naive T cells through the regulation of IL-7Rα expression.
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Immune homeostasis: Balancing the gut
p848 | doi:10.1038/nri3577
The histone deacetylase HDAC3 in IECs regulates host-commensal bacteria interactions and maintains intestinal homeostasis.
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IN BRIEF

T cell responses: NFIL3 clocks out TH17 cells | Autoimmunity: Altered microbiota linked to rheumatoid arthritis | Parasite immunity: IL-6 helps the regulators rein in TH2 cells | B cells: The adjuvant action of bisphosphonates | Antibodies: Kupffer cells mediate B cell depletion | Macrophages: BACH2 normal
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REVIEWS

Top
Studying immunity to zoonotic diseases in the natural host — keeping it real
Andrew G. D. Bean, Michelle L. Baker, Cameron R. Stewart, Christopher Cowled, Celine Deffrasnes, Lin-Fa Wang & John W. Lowenthal
p851 | doi:10.1038/nri3551
Immunology is traditionally viewed as a science of 'mice and men'. However, key insights can come from the study of immune responses in livestock or wild animals. The fact that the most deadly pathogens of humans are often zoonotic in nature lends further weight to the importance of this research. The authors discuss the benefits of, and challenges posed by, these studies.
Abstract | Full Text | PDF | Supplementary information


Sepsis-induced immunosuppression: from cellular dysfunctions to immunotherapy
Richard S. Hotchkiss, Guillaume Monneret & Didier Payen
p862 | doi:10.1038/nri3552
Sepsis is the host inflammatory response to severe, life-threatening infection with the presence of organ dysfunction, and is the most frequent cause of mortality in most intensive care units. Here, the authors argue that, following survival of the initial hyper-inflammatory response, the patient enters a protracted immunosuppressive phase and, therefore, that immunotherapies to treat prolonged sepsis must target the specific cellular dysfunctions associated with immunosuppression.
Abstract | Full Text | PDF


Age-dependent dysregulation of innate immunity
Albert C. Shaw, Daniel R. Goldstein & Ruth R. Montgomery
p875 | doi:10.1038/nri3547
Ageing is associated with impaired immune responses to pathogens and vaccines. As described in this Review, ageing results in disrupted regulation of immune cell functions and innate immune receptor signalling, and in the establishment of a persistent pro-inflammatory milieu. The authors explain how this age-associated dysregulation might contribute to chronic inflammatory diseases in the elderly.
Abstract | Full Text | PDF


The immunobiology of prion diseases
Adriano Aguzzi, Mario Nuvolone & Caihong Zhu
p888 | doi:10.1038/nri3553
Prions are infectious proteins that cause fatal neurodegenerative diseases. The prion itself is a misfolded conformer of a normal host protein, which explains why it is difficult for the immune system to respond to it effectively. The authors explain how prions evade, and indeed exploit, immune components to spread to the central nervous system, and they discuss the immunotherapies that are being developed to combat these lethal infections.
Abstract | Full Text | PDF


 
CORRESPONDENCE

Top
Primary lysis of eosinophils as a major mode of activation of eosinophils in human diseased tissues
Carl Persson & Lena Uller
p902 | doi:10.1038/nri3341-c1
Full Text | PDF

Reply to Eosinophil cytolysis and release of cell-free granules
Helene F. Rosenberg & Paul S. Foster
p902 | doi:10.1038/nri3341-c2
Full Text | PDF

miR-122, IL28B genotype and the response to interferon in chronic hepatitis C virus infection
Jae Il Shin & Michael Eisenhut
p902 | doi:10.1038/nri3463-c1
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Reply to miR-122, IL28B genotype and the response to interferon in chronic hepatitis C virus infection
Markus Heim
p902 | doi:10.1038/nri3463-c2
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