Tuesday, July 7, 2015

Nature Medicine Contents: July 2015 Volume 21 Number 7 pp 655 - 827

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Nature Medicine

TABLE OF CONTENTS

July 2015 Volume 21, Issue 7

Focus
News
News and Views
Editorial
Reviews
Articles
Letters
Errata
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Focus

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Focus on inflammatory disease   

News

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All aboard: Will molecular tumor boards help cancer patients?   pp655 - 656
Jeanne Erdmann
doi:10.1038/nm0715-655

Almighty antibodies? A new wave of antibody-based approaches aims to combat HIV   pp657 - 659
Erika Check Hayden
doi:10.1038/nm0715-657

Biomedical briefing   pp660 - 661
doi:10.1038/nm0715-660

To build better tuberculosis diagnostics, look for 'biosignatures'   p662
Alan Dove
doi:10.1038/nm0715-662

News and Views

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Liquid biopsies reveal the dynamic nature of resistance mechanisms in solid tumors   pp663 - 665
Catherine B Meador and Christine M Lovly
doi:10.1038/nm.3899
Two new studies demonstrate that so-called 'liquid biopsies' may reveal important genomic information needed to monitor treatment responses, forecast tumor recurrences, and provide a rationale for novel therapeutic strategies in patients with lung cancer and colon cancer.

See also: Letter by Siravegna et al.

Shifts in macrophage cytokine production drive muscle fibrosis   pp665 - 666
James G Tidball and Michelle Wehling-Henricks
doi:10.1038/nm.3896
Muscle fibrosis after acute injury can be debilitating, but in chronic muscle disease it can be lethal. A new study reveals that shifts in macrophage phenotype in injured or diseased muscle can influence whether connective tissue production by fibro/adipogenic precursors in muscle is beneficial or pathological.

See also: Article by Lemos et al.

Tracing human brown fat   pp667 - 668
Mariette R Boon, Emmani B M Nascimento and Wouter D van Marken Lichtenbelt
doi:10.1038/nm.3900
Adipocyte progenitors have the capacity to differentiate into mature brown adipocytes with thermogenic capabilities. Two new studies identify novel markers to help prospectively isolate these and mature adipocytes from human brown fat biopsies.

See also: Article by Xue et al.

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Editorial

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Big data meets mechanism   p673
doi:10.1038/nm.3903
Inflammatory disease research is burgeoning. Large data sets are being generated to characterize the human immune response, while detailed mechanistic studies are defining the role of specific cell types and sensors in inflammatory disease. Future efforts are needed to integrate these approaches and guide precision medicine.

News

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A gut feeling about immunity   pp674 - 676
Roxanne Khamsi
doi:10.1038/nm.3906
As it becomes evident that the microbiome exerts an influence on the human immune system, scientists have begun to ponder therapies that might act on intestinal microbes to reduce harmful inflammation. Roxanne Khamsi reports.

Reviews

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Inflammasomes: mechanism of action, role in disease, and therapeutics   pp677 - 687
Haitao Guo, Justin B Callaway and Jenny P-Y Ting
doi:10.1038/nm.3893

The emerging role of resident memory T cells in protective immunity and inflammatory disease   pp688 - 697
Chang Ook Park and Thomas S Kupper
doi:10.1038/nm.3883
Tissue-resident memory T cells are increasingly being linked to human tissue-specific immune and inflammatory disease. These roles are discussed in this review.

Innate lymphoid cells in the initiation, regulation and resolution of inflammation   pp698 - 708
Gregory F Sonnenberg and David Artis
doi:10.1038/nm.3892
The role of innate lymphoid cells (ILCs) in immune homeostasis and disease is reviewed.

Influence of nutrient-derived metabolites on lymphocyte immunity   pp709 - 718
Marc Veldhoen and Cristina Ferreira
doi:10.1038/nm.3894
Recent studies have provided insight into how the environment, and in particular the diet, influence the development of lymphocytes. Emerging studies indicate a role for this immune development in inflammatory disease.

IL-12 and IL-23 cytokines: from discovery to targeted therapies for immune-mediated inflammatory diseases   pp719 - 729
Michele W L Teng, Edward P Bowman, Joshua J McElwee, Mark J Smyth, Jean-Laurent Casanova et al.
doi:10.1038/nm.3895
Cua and colleagues discuss the cellular and molecular rationale for targeting IL-12 and IL-23 for therapeutic purposes in inflammatory diseases; they also review existing clinical data, discuss potential side effects, and propose future directions for targeting these cytokines in additional disorders.

Heterogeneity of autoimmune diseases: pathophysiologic insights from genetics and implications for new therapies   pp730 - 738
Judy H Cho and Marc Feldman
doi:10.1038/nm.3897
Recent advances in genetics have deepened our understanding of the pathogenic mechanisms behind autoimmune and immune-mediated diseases. This has revealed both shared pathways and a considerable degree of heterogeneity between diseases.

Articles

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Epigenetic activation of a cryptic TBC1D16 transcript enhances melanoma progression by targeting EGFR   pp741 - 750
Miguel Vizoso, Humberto J Ferreira, Paula Lopez-Serra, F Javier Carmona, Anna Martinez-Cardus et al.
doi:10.1038/nm.3863
Epigenetic inactivation of a Rab GTPase activating protein confers metastatic properties in melanoma, and it correlates with poor prognosis but better sensitivity to therapy by targeting EGFR signaling.

Subclonal diversification of primary breast cancer revealed by multiregion sequencing   pp751 - 759
Lucy R Yates, Moritz Gerstung, Stian Knappskog, Christine Desmedt, Gunes Gundem et al.
doi:10.1038/nm.3886
Whole-genome and targeted sequencing of multiple sections of each of 50 tumors reveals varying degrees of subclonal diversification and genomic heterogeneity.

Clonal analyses and gene profiling identify genetic biomarkers of the thermogenic potential of human brown and white preadipocytes   pp760 - 768
Ruidan Xue, Matthew D Lynes, Jonathan M Dreyfuss, Farnaz Shamsi, Tim J Schulz et al.
doi:10.1038/nm.3881
Human brown and white preadipocyte clones from neck fat depots have been isolated and used to identify genetic biomarkers that predict their thermogenic capacity.

See also: News and Views by Boon et al.

Urocortin3 mediates somatostatin-dependent negative feedback control of insulin secretion   pp769 - 776
Talitha van der Meulen, Cynthia J Donaldson, Elena Caceres, Anna E Hunter, Christopher Cowing-Zitron et al.
doi:10.1038/nm.3872
Ucn3 is released from pancreatic beta cells along with insulin, and it engages a negative feedback loop by promoting somatostatin secretion from delta cells to control further insulin secretion.

Selective enhancement of endothelial BMPR-II with BMP9 reverses pulmonary arterial hypertension   pp777 - 785
Lu Long, Mark L Ormiston, Xudong Yang, Mark Southwood, Stefan Graf et al.
doi:10.1038/nm.3877
BMP9 activates signaling through the BMPR-II receptor in endothelial cells and reverses established disease in three animal models of pulmonary hypertension, thus pointing to a potential new treatment for this disease.

Nilotinib reduces muscle fibrosis in chronic muscle injury by promoting TNF-mediated apoptosis of fibro/adipogenic progenitors   pp786 - 794
Dario R Lemos, Farshad Babaeijandaghi, Marcela Low, Chih-Kai Chang, Sunny T Lee et al.
doi:10.1038/nm.3869
Tgf-[beta]1 contributes to fibrosis during chronic injury by abrogating Tnf-directed apoptosis of fibro/adipogenic progenitor cells during muscle regeneration

See also: News and Views by Tidball & Wehling-Henricks

Letters

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Clonal evolution and resistance to EGFR blockade in the blood of colorectal cancer patients   pp795 - 801
Giulia Siravegna, Benedetta Mussolin, Michela Buscarino, Giorgio Corti, Andrea Cassingena et al.
doi:10.1038/nm.3870
By monitoring cfDNA, the authors reveal the dynamic adaption of clonal populations in colorectal cancer patients treated with anti-EGFR therapy, suggesting that therapeutic re-challenge may have some benefit.

See also: News and Views by Meador & Lovly

Inhibition of amyloid-[beta] plaque formation by [alpha]-synuclein   pp802 - 807
Teresa Bachhuber, Natalie Katzmarski, Joanna F McCarter, Desiree Loreth, Sabina Tahirovic et al.
doi:10.1038/nm.3885
The introduction of [alpha]-synuclein into mouse models of Alzheimer's disease, either by intracerebral injection or transgenic overexpression, is found to inhibit the formation of hippocampal amyloid-[beta] plaques.

Activation of HIF-1[alpha] and LL-37 by commensal bacteria inhibits Candida albicans colonization   pp808 - 814
Di Fan, Laura A Coughlin, Megan M Neubauer, Jiwoong Kim, Min Soo Kim et al.
doi:10.1038/nm.3871
Andrew Koh and colleagues report that gut anaerobes in adult mice prevent Candida albicans colonization by inducing an antimicrobial peptide.

Diabetes primes neutrophils to undergo NETosis, which impairs wound healing   pp815 - 819
Siu Ling Wong, Melanie Demers, Kimberly Martinod, Maureen Gallant, Yanming Wang et al.
doi:10.1038/nm.3887
Neutraphil extracellular trap formation is increased in type 1 and 2 diabetes and impairs wound healing.

Interleukin 18 function in atherosclerosis is mediated by the interleukin 18 receptor and the Na-Cl co-transporter   pp820 - 826
Jing Wang, Chongxiu Sun, Norbert Gerdes, Conglin Liu, Mengyang Liao et al.
doi:10.1038/nm.3890
Interleukin 18 function in atherosclerosis is mediated by the interleukin 18 receptor and the Na-Cl co-transporter.

Errata

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Erratum: Functionally defined therapeutic targets in diffuse intrinsic pontine glioma   p827
Catherine S Grasso, Yujie Tang, Nathalene Truffaux, Noah E Berlow, Lining Liu et al.
doi:10.1038/nm0715-827a

Erratum: Clonal evolution and resistance to EGFR blockade in the blood of colorectal cancer patients   p827
Giulia Siravegna, Benedetta Mussolin, Michela Buscarino, Giorgio Corti, Andrea Cassingena et al.
doi:10.1038/nm0715-827b

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