Monday, November 19, 2018

Nature Immunology Contents: December 2018 Volume 19  Issue 12

Nature Immunology


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TABLE OF CONTENTS

December 2018 Volume 19, Issue 12

Research Highlights
News & Views
Review Articles
Articles
Resources

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Announcing The Global Grants for Gut Health

The Global Grants for Gut Health is a competitive programme for investigator-initiated research into the human gut microbiota, supported by Yakult and Nature Research.

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The application for the Harvard Medical School Master of Medical Sciences in Immunology program is now open! The MMSc in Immunology is a comprehensive two-year program in basic and clinical immunology, including extensive coursework and laboratory-based research with leading Harvard faculty.
To learn more, please visit http://mmscimmunology.hms.harvard.edu/.
 

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Nature Outline: Ulcerative Colitis

Ulcerative colitis is a debilitating and incurable condition. But researchers have found fresh angles of attack, and a host of upcoming treatments raise the prospect of a durable victory against this common form of inflammatory bowel disease.

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Research Highlights

Villus regional heterogeneity    p1277
Ioana Visan
doi:10.1038/s41590-018-0266-0

Rules of engagement    p1277
Ioana Visan
doi:10.1038/s41590-018-0267-z

Metabolic crosstalk    p1277
Laurie A. Dempsey
doi:10.1038/s41590-018-0268-y

Microglial activity in brain injury    p1277
Zoltan Fehervari
doi:10.1038/s41590-018-0270-4

Treg cell tune-up    p1277
Zoltan Fehervari
doi:10.1038/s41590-018-0271-3

Immunology
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News & Views

LAG-3: a very singular immune checkpoint    pp1278 - 1279
Yuan Lui & Simon J. Davis
doi:10.1038/s41590-018-0257-1

CD8 helps TCR catch slippery self pMHC    pp1280 - 1281
Omer Dushek & Michael L. Dustin
doi:10.1038/s41590-018-0261-5

Tumors sweeten macrophages with acids    pp1281 - 1283
Hiroki Sekine, Masayuki Yamamoto & Hozumi Motohashi
doi:10.1038/s41590-018-0258-0

TCF-1 takes HEB up a Notch    pp1283 - 1285
Christelle Harly & Thomas Ciucci
doi:10.1038/s41590-018-0263-3

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Review Articles

The epithelial immune microenvironment (EIME) in atopic dermatitis and psoriasis    pp1286 - 1298
Teruki Dainichi, Akihiko Kitoh, Atsushi Otsuka, Saeko Nakajima, Takashi Nomura et al.
doi:10.1038/s41590-018-0256-2

Kabashima and colleagues review inflammatory skin disorders by discussing the pathogenesis of atopic dermatitis and psoriasis.

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Why is innate immunity an under-appreciated aspect of immunotherapy?

Researchers have now identified methods to elicit the innate immune system to exhibit heightened anti-infective activity while at the same time decreasing the inflammatory response.

Could this offer a new approach for immunotherapy? Read more here »

In association with Soligenix
 

Articles

Inflammation induced by influenza virus impairs human innate immune control of pneumococcus    pp1299 - 1308
Simon P. Jochems, Fernando Marcon, Beatriz F. Carniel, Mark Holloway, Elena Mitsi et al.
doi:10.1038/s41590-018-0231-y

Pneumococcal carriage in the upper respiratory tract is an important determinant of influenza severity. Jochems et al. use human systems analysis to show that influenza-induced inflammation increases bacterial burden in the nasal cavity with implications for secondary bacterial pneumonia.

Autocrine–paracrine prostaglandin E2 signaling restricts TLR4 internalization and TRIF signaling    pp1309 - 1318
Darren J. Perkins, Katharina Richard, Anne-Marie Hansen, Wendy Lai, Shreeram Nallar et al.
doi:10.1038/s41590-018-0243-7

Endosomal TLR4 signaling activates type I interferons via a TRIF-dependent pathway. Vogel and colleagues identify autocrine production of PGE2–EP4–cAMP as a negative regulator of the TRIF pathway that suppresses IFN-β expression induced by Gram-negative bacteria.

Tumor immunoevasion via acidosis-dependent induction of regulatory tumor-associated macrophages    pp1319 - 1329
Toszka Bohn, Steffen Rapp, Natascha Luther, Matthias Klein, Till-Julius Bruehl et al.
doi:10.1038/s41590-018-0226-8

Tumors can vary in both their control by immunosurveillance and their glycolytic activity. Bopp and colleagues demonstrate that highly glycolytic tumors acidify their microenvironment and use this to initiate a mechanism of localized immunosuppression.

Metabolic reprogramming of natural killer cells in obesity limits antitumor responses    pp1330 - 1340
Xavier Michelet, Lydia Dyck, Andrew Hogan, Roisin M. Loftus, Danielle Duquette et al.
doi:10.1038/s41590-018-0251-7

Obesity is a risk factor for cancer. Lynch and colleagues show that obesity alters the cellular metabolism of natural killer cells and decreases their antitumor surveillance and effector responses.

Myeloid-derived suppressor cells control B cell accumulation in the central nervous system during autoimmunity    pp1341 - 1351
Benjamin Knier, Michael Hiltensperger, Christopher Sie, Lilian Aly, Gildas Lepennetier et al.
doi:10.1038/s41590-018-0237-5

Korn and colleagues show that PMN-MDSCs restrain B cell accumulation in the central nervous system in autoimmune inflammation.

The γδTCR combines innate immunity with adaptive immunity by utilizing spatially distinct regions for agonist selection and antigen responsiveness    pp1352 - 1365
Daisy Melandri, Iva Zlatareva, Raphaël A. G. Chaleil, Robin J. Dart, Andrew Chancellor et al.
doi:10.1038/s41590-018-0253-5

Hayday and colleagues show that the responsiveness of mouse and human γδ IELs to Btnl or BTNL proteins is mediated by germline-encoded motifs within the cognate TCR Vγ chains, while Vγ chain motifs generated by somatic gene rearrangement remain available for nominal antigen binding.

TCF-1 and HEB cooperate to establish the epigenetic and transcription profiles of CD4+CD8+ thymocytes    pp1366 - 1378
Akinola Olumide Emmanuel, Stephen Arnovitz, Leila Haghi, Priya S. Mathur, Soumi Mondal et al.
doi:10.1038/s41590-018-0254-4

Thymocyte development requires a complex orchestration of multiple transcription factors. Gournari and colleagues find that Tcf-1 and HEB cooperate to establish the epigenetic and transcription profiles of CD4+CD8+ thymocytes

A TCR mechanotransduction signaling loop induces negative selection in the thymus    pp1379 - 1390
Jinsung Hong, Chenghao Ge, Prithiviraj Jothikumar, Zhou Yuan, Baoyu Liu et al.
doi:10.1038/s41590-018-0259-z

Zhu and colleagues show that negative-selection ligands induce cooperative TCR–pMHC–CD8 trimolecular 'catch bonds', whereas positive-selection ligands induce TCR–pMHC and pMHC–CD8 bimolecular 'slip bonds'.

Activated β-catenin in Foxp3+ regulatory T cells links inflammatory environments to autoimmunity    pp1391 - 1402
Tomokazu Sumida, Matthew R. Lincoln, Chinonso M. Ukeje, Donald M. Rodriguez, Hiroshi Akazawa et al.
doi:10.1038/s41590-018-0236-6

Regulatory T cells (Treg cells) can destabilize in inflammatory environments. Sumida et al. show that β-catenin signaling perturbs Treg cell function in patients with multiple sclerosis and under experimental high-salt conditions.

Human retinoic acid–regulated CD161+ regulatory T cells support wound repair in intestinal mucosa    pp1403 - 1414
Giovanni A. M. Povoleri, Estefania Nova-Lamperti, Cristiano Scottà, Giorgia Fanelli, Yun-Ching Chen et al.
doi:10.1038/s41590-018-0230-z

Treg cells are essential for enforcing peripheral tolerance but can also influence tissue regeneration. Afzali and colleagues use high-dimensional analysis to describe a distinct population of CD161+ human Treg cells involved in wound healing of the intestinal mucosa.

LAG-3 inhibits the activation of CD4+ T cells that recognize stable pMHCII through its conformation-dependent recognition of pMHCII    pp1415 - 1426
Takumi Maruhashi, Il-mi Okazaki, Daisuke Sugiura, Suzuka Takahashi, Takeo K. Maeda et al.
doi:10.1038/s41590-018-0217-9

LAG-3 is a co-inhibitory receptor on T cells, but its mode of action is controversial. Okazaki and colleagues demonstrate that LAG-3 preferentially binds stable MHC class II complexes and thereby selectively maintains tolerance of self-reactive T cells.

Resources

Bcl11b sets pro-T cell fate by site-specific cofactor recruitment and by repressing Id2 and Zbtb16    pp1427 - 1440
Hiroyuki Hosokawa, Maile Romero-Wolf, Mary A. Yui, Jonas Ungerbäck, Maria L. G. Quiloan et al.
doi:10.1038/s41590-018-0238-4

Bcl11b is needed to establish T cell–lineage identity. Rothenberg and colleagues provide a comprehensive analysis of Bcl11b–cofactor interactions and reveal the functional relevance of direct and indirect Bcl11b binding activity in thymocytes.

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Focal Point on Nanomedicine in Japan

- A race against time and old age -

Nanomedicine is on the frontline of Japan's efforts to revitalise its economy, and it may pre-emptively solve some of the world's toughest problems to boot.
 
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