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2016/01/28

Nature Reviews Rheumatology - Table of Contents alert Volume 12 Issue 2

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Nature Reviews Rheumatology

 
TABLE OF CONTENTS
 
February 2016 Volume 12 Number 2

Nature Reviews Rheumatology cover
Impact Factor 9.845 *
In this issue
Research Highlights
Year in Review
Reviews
Perspectives

Also this month
 YEAR IN REVIEW:
Inflammation in rheumatology in 2015: New tools to tackle inflammatory arthritis
Charles A. Dinarello & Leo A. B. Joosten
Glucocorticoids in 2015: New answers to old problems
Sarah A. Jones & Eric F. Morand
Systemic lupus erythematosus in 2015: Cellular and metabolic requirements of effector T cells
George C. Tsokos




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RESEARCH HIGHLIGHTS

Top

Rheumatoid arthritis: Osteoclasts and ACPAs — the joint link
Published online: 17 December 2015
p69 | doi:10.1038/nrrheum.2015.177

PDF


Rheumatoid arthritis: PIAS3 inhibition blocks FLS activity
Published online: 05 January 2016
p70 | doi:10.1038/nrrheum.2015.182

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Osteoarthritis: Osteophyte formation involves PAR2
Published online: 22 January 2016
p70 | doi:10.1038/nrrheum.2016.6

PDF


Osteoarthritis: Chondrocyte clock maintains cartilage tissue
Published online: 05 January 2016
p71 | doi:10.1038/nrrheum.2015.183

PDF


Autoimmunity: A controlled performance by BAMBI
Published online: 22 January 2016
p72 | doi:10.1038/nrrheum.2016.5

PDF


Spondyloarthropathies: IL-17A blockade ameliorates ankylosing spondylitis
Published online: 22 January 2016
p72 | doi:10.1038/nrrheum.2016.7

PDF



IN BRIEF

Rheumatoid arthritis: Having any parent with RA increases disease risk | Connective tissue diseases: Multiple pathways to sex biases in autoimmunity | Pain: Exercise aids low back pain, but the choice is yours
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YEAR IN REVIEW

Top
Glucocorticoids in 2015: New answers to old problems
Sarah A. Jones & Eric F. Morand
Published online: 24 December 2015
p73 | doi:10.1038/nrrheum.2015.176
Since glucocorticoids were first used to treat patients with rheumatoid arthritis in 1949, they have become the most common therapy for inflammatory disorders; however, their use is associated with major metabolic adverse events. Here, we review three 2015 reports with clinical and fundamental implications for the use of glucocorticoid therapy in rheumatology.
Full Text | PDF


Systemic lupus erythematosus in 2015: Cellular and metabolic requirements of effector T cells
George C. Tsokos
Published online: 05 January 2016
p74 | doi:10.1038/nrrheum.2015.178
Key advances in lupus research in 2015 highlight the contribution of T cells to the pathogenesis of the disease. The findings not only shed light on the regulation and activity of these cells, but also suggest several novel therapeutic targets.
Full Text | PDF


Psoriatic arthritis in 2015: Advancement continues in imaging, tight control and new drugs
Ignazio Olivieri & Salvatore D'Angelo
Published online: 22 January 2016
p76 | doi:10.1038/nrrheum.2015.184
In 2015, a EULAR task force released evidence-based recommendations on the use of imaging in the clinical management of spondyloarthritis, including psoriatic arthritis. These recommendations, together with articles dealing with tight control strategies and use of the IL-17A inhibitor secukinumab, have consolidated progress in the management of psoriatic arthritis.
Full Text | PDF


Inflammation in rheumatology in 2015: New tools to tackle inflammatory arthritis
Charles A. Dinarello & Leo A. B. Joosten
Published online: 14 January 2016
p78 | doi:10.1038/nrrheum.2015.180
Novel therapies to reduce the progressive and destructive nature of inflammatory joint disease are always welcome, provided that safety is not compromised. Among the many 2015 studies in the field, we highlight a targetable mechanism of uric-acid-induced inflammation in gouty arthritis and the expected efficacy — but unforeseen safety concerns — of anti-IL-17 antibodies.
Full Text | PDF



 
REVIEWS

Top
Genetics of ankylosing spondylitis—insights into pathogenesis
Matthew A. Brown, Tony Kenna & B. Paul Wordsworth
Published online: 06 October 2015
p81 | doi:10.1038/nrrheum.2015.133
Several genetic associations have been identified in patients with spondyloarthropathies, particularly ankylosing spondylitis (AS). The most recent associations uncovered which involve genes in the IL-17/IL-23 pathway enabled a better understanding of the aetiology of spondyloarthropathies, and informed the use of previously existing drugs to treat patients with these diseases—an example of how translation of hypothesis-free medical research can yield new therapeutic strategies.
Abstract | Full Text | PDF


Strategies for the prevention of knee osteoarthritis
Ewa M. Roos & Nigel K. Arden
Published online: 06 October 2015
p92 | doi:10.1038/nrrheum.2015.135
Osteoarthritis (OA) is a chronic condition that is associated with pain and disability. In this Review, Roos and Arden consider the strategies that are available for modification of risk factors contributing to the development of knee OA. Interventions for prevention and early care of knee OA could help to avoid joint-replacement surgery.
Abstract | Full Text | PDF


Anti-DNA antibodies — quintessential biomarkers of SLE
David S. Pisetsky
Published online: 19 November 2015
p102 | doi:10.1038/nrrheum.2015.151
Anti-DNA antibodies are serological hallmarks of systemic lupus erythematosus, but many questions remain unanswered regarding their origins and pathological properties, as well as the relative merits of different assay formats. Understanding the mechanisms of DNA binding and pathogenesis relating to anti-DNA antibodies can aid the development of diagnostic and theranostic assays.
Abstract | Full Text | PDF


Targeting of proangiogenic signalling pathways in chronic inflammation
Sander W. Tas, Chrissta X. Maracle, Emese Balogh & Zoltán Szekanecz
Published online: 03 December 2015
p111 | doi:10.1038/nrrheum.2015.164
Proangiogenic signalling pathways are activated in chronic inflammation, but although antiangiogenic treatments are routinely incorporated into cancer therapy, surprisingly few clinical trials have investigated this approach in patients with chronic inflammatory diseases. However, this situation could soon change — a wide range of small-molecule inhibitors with improved specificity, and techniques to target such inhibitors to specific cell types, are currently undergoing clinical and preclinical development.
Abstract | Full Text | PDF



 
PERSPECTIVES

Top
OPINION
Does lipopolysaccharide-mediated inflammation have a role in OA?
Zeyu Huang & Virginia Byers Kraus
Published online: 10 December 2015
p123 | doi:10.1038/nrrheum.2015.158
Lipopolysaccharide derived from gastrointestinal microbiota contributes to systemic inflammation and obesity. Huang and Kraus propose that lipopolysaccharide is a major risk factor for osteoarthritis (OA), and suggest that therapeutic strategies for the reduction of systemic levels of lipopolysaccharide should be considered for prevention and treatment of OA.
Abstract | Full Text | PDF


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*Journal Citation Reports, Thomson, 2014. Nature Reviews Rheumatology was previously published as Nature Clinical Practice Rheumatology.

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