Tuesday, June 21, 2016

Nature Immunology Contents: July 2016 Volume 17 pp 741 - 887

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Nature Immunology

TABLE OF CONTENTS

July 2016 Volume 17, Issue 7

Focus
Correspondence
News and Views
Research Highlights
Editorial
Comment
Reviews
Perspectives
Articles
Resource
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Immune Profiling in Health and Disease

Presented by: Adaptive Biotechnologies | Nature Immunology | Nature Medicine | Nature Biotechnology | Nature Genetics

October 3-5, 2016 | Bell Harbor International Conference Center, Seattle, WA, USA
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Focus

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Focus on Innate lymphoid cells
Innate lymphoid cells (ILCs) are a recently described family of lymphoid effector cells with important roles in immunological defense and tissue remodeling. Nature Immunology presents a series of specially commissioned articles that discuss the evolution, development, functional diversity and immunotherapeutic potential of ILCs. In collaboration with Nucleus Medical Media, Nature Immunology has also produced an animation that shows the complexity of ILC biology in the gut at steady state and during disease.
Produced with support from MedImmune
Animation by Nucleus Medical Media

Correspondence

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Open-source ImmGen: mononuclear phagocytes   p741
the ImmGen Consortium:  Christophe Benoist
doi:10.1038/ni.3478

News and Views

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Family ties among CNS macrophages   pp742 - 743
Melanie Greter
doi:10.1038/ni.3490
Perivascular and subdural meningeal macrophages at the interface between the central nervous system and the periphery are self-renewing and arise from early embryonic precursors. Macrophages residing in the choroid plexus have dual origin, developing from circulating bone-marrow-derived monocytes and embryonic progenitors.

See also: Article by Goldmann et al.

Bach2 is required for B cell and T cell memory differentiation   pp744 - 745
Tom Sidwell and Axel Kallies
doi:10.1038/ni.3493
B cell and T cell memory differentiation requires the transcription factor Bach2, which inhibits the effector-cell fate by limiting antigen-receptor-stimulation-induced gene expression and restricting premature expression of the transcriptional regulator Blimp-1.

See also: Article by Roychoudhuri et al. | Article by Shinnakasu et al.

Unchaining NK cell-mediated anticancer immunosurveillance   pp746 - 747
Laurence Zitvogel and Guido Kroemer
doi:10.1038/ni.3471
In natural killer (NK) cells, CIS restrains a signaling pathway elicited by interleukin 15 (IL-15) that leads to activation of the kinase JAK1. Removal of CIS from NK cells increases their capacity to reduce the metastatic dissemination of breast cancer and melanoma in mice.

See also: Article by Delconte et al.

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Research Highlights

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Keeping on top of inflammation | Coping with stress | Acetate for memory | The tryptophan link | Nucleocytoplasmic danger signals | Neuronal antibody access

Editorial

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Focus on Innate lymphoid cells
A versatile cell population   p754
doi:10.1038/ni.3496
Innate lymphoid cells serve multiple roles in maintaining tissue homeostasis and responding to tissue insults and can contribute to chronic inflammatory diseases.

Comment

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Focus on Innate lymphoid cells
Innate lymphoid cells in defense, immunopathology and immunotherapy   pp755 - 757
Sascha Cording, Jasna Medvedovic, Tegest Aychek and Gérard Eberl
doi:10.1038/ni.3448
Targeting innate lymphoid cells, the innate counterparts of T cells, might help direct an appropriate immune response during preventive and therapeutic strategies aimed at pathogens and inflammatory pathologies

Reviews

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Focus on Innate lymphoid cells
NK cells and type 1 innate lymphoid cells: partners in host defense   pp758 - 764

Hergen Spits, Jochem H Bernink and Lewis Lanier
doi:10.1038/ni.3482
NK cells and ILC1s are developmentally distinct but share many functional similarities. Spits and colleagues describe current knowledge on the biology of these cells and the conditions under which they can be distinguished.

Focus on Innate lymphoid cells
Innate lymphoid cells as regulators of immunity, inflammation and tissue homeostasis   pp765 - 774

Christoph S N Klose and David Artis
doi:10.1038/ni.3489
In this Review, Klose and Artis focus on how group 2 ILC and group 3 ILC responses are regulated and how they interact with other immune and non-immune cells to mediate their functions.

Focus on Innate lymphoid cells
Development of innate lymphoid cells   pp775 - 782

Erin C Zook and Barbara L Kee
doi:10.4038/ni.3481
Innate lymphoid cells (ILCs) arise from distinct hematopoietic progenitors. Zook & Kee discuss the transcriptional programs that direct the development of natural killer cells and various ILC subsets.

Perspectives

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Focus on Innate lymphoid cells
Innate lymphoid cell function in the context of adaptive immunity   pp783 - 789

Jennifer K Bando and Marco Colonna
doi:10.1038/ni.3484
The redundant or specialized roles of innate lymphoid cells (ILCs) relative to those of T cells in vivo remain hard to delineate experimentally. Bando and Colonna review the current understanding of the specialized in vivo functions of ILCs and discuss the genetic mouse models used to assess the contributions of ILCs versus those of T cells.

Focus on Innate lymphoid cells
The evolution of innate lymphoid cells   pp790 - 794
Eric Vivier, Serge A van de Pavert, Max D Cooper and Gabrielle T Belz
doi:10.1038/ni.3459
The appearance of innate lymphoid cells was a major step in the evolution of vertebrate immunity. In their Perspective, Vivier et al. survey these cells in evolution and their functional inter-relationship with conventional T cells and B cells.

Articles

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Origin, fate and dynamics of macrophages at central nervous system interfaces   pp797 - 805
Tobias Goldmann, Peter Wieghofer, Marta Joana Costa Jordão, Fabiola Prutek, Nora Hagemeyer et al.
doi:10.1038/ni.3423
Microglia progenitors seed the central nervous system from the yolk sac, but little is known about the origin of non-parenchymal macrophages. Prinz and colleagues demonstrate that these macrophages in the central nervous system are related to but distinct from microglia and are largely of embryonic origin.

See also: Article by Goldmann et al.

Methyltransferase Dnmt3a upregulates HDAC9 to deacetylate the kinase TBK1 for activation of antiviral innate immunity   pp806 - 815
Xia Li, Qian Zhang, Yuanyuan Ding, Yiqi Liu, Dezhi Zhao et al.
doi:10.1038/ni.3464
The DNA methyltransferase Dnmt3a has not been studied in innate immunity. Cao and colleagues show that Dnmt3a enhances antiviral responses via a non-canonical mechanism to activate the kinase TBK1 and the production of type I interferons in macrophages.

CIS is a potent checkpoint in NK cell-mediated tumor immunity   pp816 - 824
Rebecca B Delconte, Tatiana B Kolesnik, Laura F Dagley, Jai Rautela, Wei Shi et al.
doi:10.1038/ni.3470
IL-15-driven NK cells mediate anti-tumor immunity, but how IL-15 is negatively regulated remains unclear. Huntington and colleagues find that CIS, a member of the suppressor of cytokine signaling family, suppresses the response to IL-15 and, as a result, CIS-deficient mice are more resistant to cancer metastasis.

See also: News and Views by Zitvogel & Kroemer

A TRAF-like motif of the inducible costimulator ICOS controls development of germinal center TFH cells via the kinase TBK1   pp825 - 833
Christophe Pedros, Yaoyang Zhang, Joyce K Hu, Youn Soo Choi, Ann J Canonigo-Balancio et al.
doi:10.1038/ni.3463
Signaling via the inducible costimulator ICOS drives the stepwise development of follicular helper T cells. Kong and colleagues describe an ICOS-kinase TBK1 signaling pathway that specifies the commitment of these cells.

Id2 reinforces TH1 differentiation and inhibits E2A to repress TFH differentiation   pp834 - 843
Laura A Shaw, Simon Bélanger, Kyla D Omilusik, Sunglim Cho, James P Scott-Browne et al.
doi:10.1038/ni.3461
Activation of CD4+ T cells leads to their polarization to various effector states. Goldrath and colleagues identify a role for the E-protein inhibitor Id2 in promoting TH1 cell polarization over TFH cell polarization. Reciprocally, the transcription factor Bcl-6 represses Id2 expression in TFH cells.

Inhibition of T cell receptor signaling by cholesterol sulfate, a naturally occurring derivative of membrane cholesterol   pp844 - 850
Feng Wang, Katharina Beck-García, Carina Zorzin, Wolfgang W A Schamel and Mark M Davis
doi:10.1038/ni.3462
Davis and colleagues show that cholesterol sulfate, a naturally occurring analog of cholesterol, regulates CD3ζ phosphorylation and thymic selection.

BACH2 regulates CD8+ T cell differentiation by controlling access of AP-1 factors to enhancers   pp851 - 860
Rahul Roychoudhuri, David Clever, Peng Li, Yoshiyuki Wakabayashi, Kylie M Quinn et al.
doi:10.1038/ni.3441
T cell activation upon TCR signaling can lead to development of effector and memory cells. Roychoudhuri and colleagues show that the transcription factor BACH2 promotes memory CD8+ T cell generation by blocking access to genomic regulatory sites recognized by AP-1.

See also: News and Views by Sidwell & Kallies

Regulated selection of germinal-center cells into the memory B cell compartment   pp861 - 869
Ryo Shinnakasu, Takeshi Inoue, Kohei Kometani, Saya Moriyama, Yu Adachi et al.
doi:10.1038/ni.3460
T cells provide help to B cells in germinal centers. Kurosaki and colleagues show that B cells of lower affinity receive weaker T cell help. This scenario results in higher expression of the transcriptional repressor Bach2 and promotes the development of memory B cells.

See also: News and Views by Sidwell & Kallies

Germinal center B cells recognize antigen through a specialized immune synapse architecture   pp870 - 877
Carla R Nowosad, Katelyn M Spillane and Pavel Tolar
doi:10.1038/ni.3458
B cells can capture antigen to present to helper T cells. Tolar and colleagues show that germinal center B cells use a distinct synaptic architecture to capture antigen with higher mechanical forces than those of other B cells, which might provide the basis for affinity discrimination.

Resource

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Expression profiling of constitutive mast cells reveals a unique identity within the immune system   pp878 - 887
Daniel F Dwyer, Nora A Barrett, K Frank Austen and The Immunological Genome Project Consortium
doi:10.1038/ni.3445
Austen and colleagues assess the transcriptional profiles of mast cells isolated from peripheral connective tissues and basophils isolated from spleen and blood. Mast cells show a unique tissue profile and minimal homology with basophils or other immunocytes.

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