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July 2017 Volume 17 Number 7 | Advertisement | ||||||||||||||||||||||||||||||||||||||||
In this issue Research Highlights Reviews Perspectives
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REVIEWS | Top | ||||||||||||||||||||||||||||||||||||||||
The immunopathology of sepsis and potential therapeutic targets Tom van der Poll, Frank L. van de Veerdonk, Brendon P. Scicluna & Mihai G. Netea p407 | doi:10.1038/nri.2017.36 Sepsis — which is caused by a dysregulated host response to infection — is a life-threatening organ dysfunction. This Review describes the recent advances in our understanding of sepsis pathogenesis and discusses strategies for the development of successful therapies. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||
Altered B cell signalling in autoimmunity David J. Rawlings, Genita Metzler, Michelle Wray-Dutra & Shaun W. Jackson p421 | doi:10.1038/nri.2017.24 In this Review, the authors propose that disease-associated genetic variants modulate signalling downstream of B cell receptors, Toll-like receptors and cytokine receptors in B cells to drive autoimmune responses. This altered signalling favours a naive B cell repertoire that is skewed towards self-reactivity and promotes the peripheral activation of autoreactive B cell clones. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||
BACH transcription factors in innate and adaptive immunity Kazuhiko Igarashi, Tomohiro Kurosaki & Rahul Roychoudhuri p437 | doi:10.1038/nri.2017.26 The transcriptional repressors BTB and CNC homology 1 (BACH1) and BACH2 compete with transcriptional activators of the basic region leucine zipper (bZIP) family to control widespread functions of the innate and adaptive immune systems. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||
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PERSPECTIVES | Top | ||||||||||||||||||||||||||||||||||||||||
OPINION Does niche competition determine the origin of tissue-resident macrophages? Martin Guilliams & Charlotte L. Scott p451 | doi:10.1038/nri.2017.42 In this Opinion article, the authors discuss the limitations of categorizing tissue-resident macrophages based on their ontogeny. Instead, they propose that competition for a limited number of tissue niches may serve as a better framework for understanding the origins and functions of tissue macrophages. Abstract | Full Text | PDF | |||||||||||||||||||||||||||||||||||||||||
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