Monday, April 23, 2018

Nature Immunology Contents: May 2018 Volume 19 Issue 5

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TABLE OF CONTENTS

May 2018 Volume 19, Issue 5

Comment
News & Views
Letters
Articles
 
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Of mice, men and immunity: a case for evolutionary systems biology    pp421 - 425
Peter B. Ernst & Anne-Ruxandra Carvunis
doi:10.1038/s41590-018-0084-4

Mice are generally the ‘go-to’ organism for modeling of the human immune system, but this often leads to inaccurate interpretations. Ernst and Carvunis argue in this Comment that taking into account the evolutionary and environmental context can generate better models of disease.

 

News & Views

 

Adaptive responses of innate lymphocytes    pp426 - 427
Carsten Watzl
doi:10.1038/s41590-018-0088-0

Got my γδ17 T cells to keep me warm    pp427 - 429
Pedro H. Papotto & Bruno Silva-Santos
doi:10.1038/s41590-018-0090-6

c-Maf in CD4+ T cells: it’s all about context    pp429 - 431
W. Nicholas Haining & Sarah A. Weiss
doi:10.1038/s41590-018-0087-1

Traumatic meningeal injury and repair mechanisms    pp431 - 432
David J. Loane & Alan I. Faden
doi:10.1038/s41590-018-0093-3

Hard-to-kill macrophages lead to chronic inflammation in HIV    pp433 - 434
Peter Kelleher & Xiao-Ning Xu
doi:10.1038/s41590-018-0089-z

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Letters

 

Fatal demyelinating disease is induced by monocyte-derived macrophages in the absence of TGF-β signaling    pp1 - 7
Harald Lund, Melanie Pieber, Roham Parsa, David Grommisch, Ewoud Ewing et al.
doi:10.1038/s41590-018-0091-5

Harris and colleagues show that the cytokine TGF-β is required for colonization of the microglial niche and maintenance of central nervous system integrity. Acute loss of TGF-β leads to proinflammatory responses and fatal demyelinating disease.

 

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Articles

 

Distinct myeloid cell subsets promote meningeal remodeling and vascular repair after mild traumatic brain injury    pp442 - 452
Matthew V. Russo, Lawrence L. Latour & Dorian B. McGavern
doi:10.1038/s41590-018-0086-2

Meningeal vascular damage accompanies mild traumatic brain injury, which persists in a fraction of patients. McGavern and colleagues report that distinct myeloid cell subsets are temporally recruited to the wound site during tissue repair; however, re-injury at early time points impairs recovery.

 

Peptide-specific recognition of human cytomegalovirus strains controls adaptive natural killer cells    pp453 - 463
Quirin Hammer, Timo Rückert, Eva Maria Borst, Josefine Dunst, André Haubner et al.
doi:10.1038/s41590-018-0082-6

NK cells constrain infection by cytomegalovirus. Romagnani and colleagues show that human NKG2C+ NK cells recognize distinct HCMV UL40 viral peptides, which can vary among viral isolates. NKG2C+ NK cells thereby demonstrate adaptive-like recognition that can discriminate between closely related viral strains.

 

γδ T cells producing interleukin-17A regulate adipose regulatory T cell homeostasis and thermogenesis    pp464 - 474
Ayano C. Kohlgruber, Shani T. Gal-Oz, Nelson M. LaMarche, Moto Shimazaki, Danielle Duquette et al.
doi:10.1038/s41590-018-0094-2

Lynch, Brenner and colleagues find that tissue-resident γδ T cells reside in adipose tissues in both mice and humans. These cells play essential roles in regulating thermogenesis and supporting age-dependent increases in adipose-tissue regulatory T cell populations.

 

Resistance of HIV-infected macrophages to CD8+ T lymphocyte–mediated killing drives activation of the immune system    pp475 - 486
Kiera L. Clayton, David R. Collins, Josh Lengieza, Musie Ghebremichael, Farokh Dotiwala et al.
doi:10.1038/s41590-018-0085-3

Macrophages can be an important niche for chronic viral infection. Walker and colleagues demonstrate that macrophages are intrinsically resistant to CTL-mediated killing and can thereby contribute to the maintenance of HIV reservoirs and chronic inflammation.

 

Monomeric TCRs drive T cell antigen recognition    pp487 - 496
Mario Brameshuber, Florian Kellner, Benedikt K. Rossboth, Haisen Ta, Kevin Alge et al.
doi:10.1038/s41590-018-0092-4

Higher-order TCRs have been postulated to maintain high antigen sensitivity and trigger signaling. Huppa and colleagues use various investigative techniques and find exclusively monomeric TCR–CD3 complexes that drive the recognition of antigenic pMHC.

 

c-Maf controls immune responses by regulating disease-specific gene networks and repressing IL-2 in CD4+ T cells    pp497 - 507
Leona Gabryšová, Marisol Alvarez-Martinez, Raphaëlle Luisier, Luke S. Cox, Jan Sodenkamp et al.
doi:10.1038/s41590-018-0083-5

The transcription factor c-Maf controls IL-10 production in T cells. O’Garra and colleagues use systems and in vivo functional analysis of T cell subsets to reveal distinct context-specific roles for c-Maf.

 

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