Tuesday, May 19, 2015

Nature Immunology Contents: June 2015 Volume 16 pp 545 - 673

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TABLE OF CONTENTS

June 2015 Volume 16, Issue 6

Focus
Editorial
Reviews
Perspective
Research Highlights
Obituary
News and Views
Research Highlights
Articles
Resource
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Focus

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Focus on The immunology of HIV
Nature Immunology presents a series of specially commissioned articles that discuss the most recent progress in understanding the immune response to HIV and how this new insight can be harnessed for prophylactic vaccines and immunotherapies.

Editorial

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Focus on The immunology of HIV
A formidable challenge   p545
doi:10.1038/ni.3179
Better understanding of HIV biology, virus-host interactions and mechanisms of an efficient immune response advance efforts for effective vaccines and immunotherapies.

Reviews

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Focus on The immunology of HIV
Intrinsic host restrictions to HIV-1 and mechanisms of viral escape   pp546 - 553
Viviana Simon, Nicolin Bloch and Nathaniel R Landau
doi:10.1038/ni.3156
HIV devotes a large portion of its coding capacity to counteracting the function of mammalian antiviral proteins. Landau and colleagues discuss the biology of mammalian restriction factors and the viral accessory proteins that counteract them.

Focus on The immunology of HIV
Innate immunity against HIV-1 infection   pp554 - 562
Marcus Altfeld and Michael Gale Jr
doi:10.1038/ni.3157
Innate effector mechanisms contribute to the control of viremia and modulate the quality of the adaptive immune response to HIV-1. Altfeld and Gale discuss the concerted actions of PRR signaling, innate immune cells and innate-adaptive crosstalk that direct the outcome of HIV-1 infection.

Focus on The immunology of HIV
Success and failure of the cellular immune response against HIV-1   pp563 - 570
Stephen A Migueles and Mark Connors
doi:10.1038/ni.3161
Understanding the success and failure of the HIV-specific cellular immune response has implications for immunotherapies and vaccines for HIV-1. Migueles and Connors discuss the mechanisms that are most likely responsible for durable and potent immunologic control of HIV-1 by the cellular immune response.

Focus on The immunology of HIV
Antibody responses to envelope glycoproteins in HIV-1 infection   pp571 - 576
Dennis R Burton and John R Mascola
doi:10.1038/ni.3158
Antibody responses to the HIV-1 envelope glycoproteins can be classified into three groups. Burton and Mascola discuss how recent insight into the structure and immunology of non-neutralizing, strain-specific and broadly neutralizing antibodies guide HIV-1 vaccine design and therapeutic strategies.

Focus on The immunology of HIV
The impact of host genetic variation on infection with HIV-1   pp577 - 583
Paul J McLaren and Mary Carrington
doi:10.1038/ni.3147
An effect of host genetic variation on susceptibility to HIV-1 was identified early in the pandemic. McLaren and Carrington discuss the extent to which additional polymorphisms influence HIV-1 disease progression and how analysis of data sets may discover novel gene variants that affect the outcome of HIV-1.

Perspective

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Focus on The immunology of HIV
HIV reservoirs as obstacles and opportunities for an HIV cure   pp584 - 589
Tae-Wook Chun, Susan Moir and Anthony S Fauci
doi:10.1038/ni.3152
The persistence of HIV reservoirs remains a barrier to sustained virologic remission in HIV-infected individuals after antiretroviral therapy is discontinued. Fauci and colleagues discuss the therapeutic strategies aimed at eliminating or controlling the virus in the absence of ART.

Research Highlights

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Focus on The immunology of HIV
Integration logistics | Neutralizing antibody evolution | HIV-1 in the driving seat | HIV keeps DCs immature | HIV entry | Passive protection

Obituary

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Paula Pitha-Rowe 1937-2015   p591
Katherine A Fitzgerald
doi:10.1038/ni.3173

News and Views

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TET1: an epigenetic guardian of lymphomagenesis   pp592 - 594
Kasper Dindler Rasmussen and Kristian Helin
doi:10.1038/ni.3176
Due to their role in regulating DNA-methylation patterns, the TET proteins, in particular TET2, have emerged as key participants in tumorigenesis. Now the spotlight shifts to TET1 and its role as a tumor suppressor in lymphomagenesis.

See also: Article by Cimmino et al.

TOX sets the stage for innate lymphoid cells   pp594 - 595
Hergen Spits
doi:10.1038/ni.3177
Like T cells and B cells, innate lymphoid cells (ILCs) develop from common lymphoid progenitors, but how commitment to the ILC lineage is regulated has remained unclear. The transcriptional regulator TOX is important in this process.

See also: Article by Seehus et al.

A20 is a regulator of necroptosis   pp596 - 597
Prajwal Gurung, Si Ming Man and Thirumala-Devi Kanneganti
doi:10.1038/ni.3174
The anti-inflammatory molecule A20 inhibits necroptotic cell death by inhibiting ubiquitination of the kinase RIPK3 at the Lys5 residue and preventing excessive formation of the RIPK1-RIPK3 necroptotic complex.

See also: Article by Onizawa et al.

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Research Highlights

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NK cell action at a distance | | Tissue-specific surveillance | Rare protein modification | Strengthening barriers | Targeting leukemic stem cells

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Articles

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The development of innate lymphoid cells requires TOX-dependent generation of a common innate lymphoid cell progenitor   pp599 - 608
Corey R Seehus, Parinaz Aliahmad, Brian de la Torre, Iliyan D Iliev, Lindsay Spurka et al.
doi:10.1038/ni.3168
The transcriptional regulation of the differentiation of innate lymphoid cells remains incompletely characterized. Kaye and colleagues show that the transcriptional regulator TOX is required for the differentiation of common lymphoid progenitors into the innate lymphoid cell lineage.

See also: News and Views by Spits

Eosinophils orchestrate cancer rejection by normalizing tumor vessels and enhancing infiltration of CD8+ T cells   pp609 - 617
Rafael Carretero, Ibrahim M Sektioglu, Natalio Garbi, Oscar C Salgado, Philipp Beckhove et al.
doi:10.1038/ni.3159
Eosinophils are commonly observed in solid tumors, but their role has remained uncertain. Hammerling and colleagues show that activated eosinophils contribute to tumor eradication by altering tumor vasculature and increasing the infiltration of CD8+ T cells.

The ubiquitin-modifying enzyme A20 restricts ubiquitination of the kinase RIPK3 and protects cells from necroptosis   pp618 - 627
Michio Onizawa, Shigeru Oshima, Ulf Schulze-Topphoff, Juan A Oses-Prieto, Timothy Lu et al.
doi:10.1038/ni.3172
A20 is a deubiquitinating enzyme that restrict inflammation by various mechanisms. Ma and colleagues show that A20 inhibits necroptosis by inhibiting the ubiquitination of RIPK3 and formation of the RIPK1-RIPK3 complex.

See also: News and Views by Gurung et al.

Peripheral regulatory T lymphocytes recirculating to the thymus suppress the development of their precursors   pp628 - 634
Nicolas Thiault, Julie Darrigues, Véronique Adoue, Marine Gros, Bénédicte Binet et al.
doi:10.1038/ni.3150
Regulatory T cells (Treg cells) can suppress autoreactive immune responses in the periphery. Joost van Meerwijk and colleagues show that activated peripheral Treg cells can recirculate back to the thymus, where they can suppress further thymic Treg cell development.

Thymic regulatory T cell niche size is dictated by limiting IL-2 from antigen-bearing dendritic cells and feedback competition   pp635 - 641
Brian M Weist, Nadia Kurd, Jeremy Boussier, Shiao Wei Chan and Ellen A Robey
doi:10.1038/ni.3171
Thymic regulatory T cells require IL-2 for their development. Robey and colleagues show that developing cells compete with pre-existing regulatory T cells for limiting amounts of IL-2 produced by antigen-bearing dendritic cells

Tyrosine phosphatase SHP-2 mediates C-type lectin receptor-induced activation of the kinase Syk and anti-fungal TH17 responses   pp642 - 652
Zihou Deng, Shixin Ma, Hao Zhou, Aiping Zang, Yiyuan Fang et al.
doi:10.1038/ni.3155
Fungal infection induces signaling downstream C-type lectin receptors through the activation of the tyrosine kinase Syk. Xiao and colleagues show that the phosphatase SHP-2 recruits Syk to dectin-1.

TET1 is a tumor suppressor of hematopoietic malignancy   pp653 - 662
Luisa Cimmino, Meelad M Dawlaty, Delphine Ndiaye-Lobry, Yoon Sing Yap, Sofia Bakogianni et al.
doi:10.1038/ni.3148
Methylation of DNA CpG motifs is modulated in part by the TET family of epigenetic regulators. Aifantis and colleagues show that loss of TET1 function biases hematopoiesis toward the B cell lineage and promotes hematopoietic malignancies.

See also: News and Views by Rasmussen & Helin

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Resource

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Transcriptional profiling of mouse B cell terminal differentiation defines a signature for antibody-secreting plasma cells   pp663 - 673
Wei Shi, Yang Liao, Simon N Willis, Nadine Taubenheim, Michael Inouye et al.
doi:10.1038/ni.3154
The process of B cell differentiation into plasma cells involves dramatic cellular reprogramming. Corcoran and colleagues profile the transcriptome of all stages of B cell differentiation through to antibody-secreting plasma cells.

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Focus on The immunology of HIV

Nature Immunology presents a series of specially commissioned articles that discuss the most recent progress in understanding the immune response to HIV and how this new insight can be harnessed for prophylactic vaccines and immunotherapies. 

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