Friday, February 15, 2013

Nature Immunology Contents: March 2013 Volume 14 pp 187 - 305

Nature Immunology

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TABLE OF CONTENTS

March 2013 Volume 14, Issue 3

Correspondence
Obituary
Commentary
News and Views
Research Highlights
Review
Articles

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Correspondence

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Can DCs be distinguished from macrophages by molecular signatures?   pp187 - 189
David A Hume, Neil Mabbott, Sobia Raza and Tom C Freeman
doi:10.1038/ni.2516

See also: Correspondence by Randolph & Merad

Reply to: "Can DCs be distinguished from macrophages by molecular signatures?"   pp189 - 190
Gwen Randolph and Miriam Merad
doi:10.1038/ni.2517

See also: Correspondence by Hume et al.

Obituary

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Brigitte Askonas 1923-2013   p191
Emil R Unanue
doi:10.1038/ni.2553

Commentary

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Can the SBIR and STTR programs advance research goals?   pp192 - 195
Steven Ceulemans and Jay K Kolls
doi:10.1038/ni.2495

News and Views

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A Tip leads cytotoxic T cells to the crime scene in neuroinflammation   pp196 - 197
Lawrence Steinman
doi:10.1038/ni.2551
By increasing the range of epitopes presented to lymphocytes, determinant spreading allows a more diverse response to ensue. Now the cellular culprits responsible for determinant spreading in the central nervous system have been identified: they are specialized dendritic cells that recruit recruiting CD8+ T cells to an autoimmune 'crime'.

See also: Article by Ji et al.

Myeloid-cell differentiation redefined in cancer   pp197 - 199
Thomas A Wynn
doi:10.1038/ni.2539
The differentiation of monocytes is altered in cancer, which results in the unexpected conversion of a large proportion of monocytic myeloid-derived suppressor cells into polymorphonuclear myeloid-derived suppressor cells.

See also: Article by Youn et al.

Changing course by lymphocyte lineage redirection   pp199 - 201
Michele K Anderson
doi:10.1038/ni.2544
The fate of T cells differentiating into the CD4 or CD8 lineage is typically fixed when cells leave the thymus. However, CD4+ helper T cells can be reprogrammed to develop into CD4+CD8α+ cytotoxic T lymphocytes in the gut.

See also: Article by Reis et al. | Article by Mucida et al.

'Nurr'ishing Treg cells: Nr4a transcription factors control Foxp3 expression   pp201 - 203
Hozefa S Bandukwala and Anjana Rao
doi:10.1038/ni.2546
The Nr4a family of transcription factors transactivate expression of the transcription factor Foxp3 and are essential for the generation of regulatory T cells. Mice deficient in all three members of the Nr4a family develop massive multiorgan inflammation.

See also: Article by Sekiya et al.

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Research Highlights

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The unusual suspects | Latent enhancement | Signal integration | Living with commensals | Gender, microbes & autoimmunity | Clipping B cells


Review

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MicroRNAs as mediators of viral evasion of the immune system   pp205 - 210
Bryan R Cullen
doi:10.1038/ni.2537

Articles

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Epigenetic silencing of retinoblastoma gene regulates pathologic differentiation of myeloid cells in cancer   pp211 - 220
Je-In Youn, Vinit Kumar, Michelle Collazo, Yulia Nefedova, Thomas Condamine, Pingyan Cheng, Alejandro Villagra, Scott Antonia, Judith C McCaffrey, Mayer Fishman, Amod Sarnaik, Pedro Horna, Eduardo Sotomayor and Dmitry I Gabrilovich
doi:10.1038/ni.2526
Gabrilovich and colleagues show that monocytic myeloid-derived suppressor cells (MDSCs) differentiate into polymorphonuclear MDSCs in individuals with tumors, demonstrating a demonstrating a distinct regulation of myeloid cell development in cancer.

See also: News and Views by Wynn

Human type 1 innate lymphoid cells accumulate in inflamed mucosal tissues   pp221 - 229
Jochem H Bernink, Charlotte P Peters, Marius Munneke, Anje A te Velde, Sybren L Meijer, Kees Weijer, Hulda S Hreggvidsdottir, Sigrid E Heinsbroek, Nicolas Legrand, Christianne J Buskens, Willem A Bemelman, Jenny M Mjosberg and Hergen Spits
doi:10.1038/ni.2534
Innate lymphoid cells are cytokine-producing cells that contribute to tissue homeostasis. Spits and colleagues identify a human innate cell population that expresses T-bet and IFN-γ and is prevalent in Crohn's disease.

Nr4a receptors are essential for thymic regulatory T cell development and immune homeostasis   pp230 - 237
Takashi Sekiya, Ikkou Kashiwagi, Rei Yoshida, Tomohiro Fukaya, Rimpei Morita, Akihiro Kimura, Hiroshi Ichinose, Daniel Metzger, Pierre Chambon and Akihiko Yoshimura
doi:10.1038/ni.2520
Sekiya and colleagues demonstrate that the Nr4a nuclear receptors, which are encoded by immediate-early genes upregulated by TCR stimulation in thymocytes, have an essential role in regulatory T cell development.

See also: News and Views by Bandukwala & Rao

Enhanced survival of lung tissue-resident memory CD8+ T cells during infection with influenza virus due to selective expression of IFITM3   pp238 - 245
Linda M Wakim, Nishma Gupta, Justine D Mintern and Jose A Villadangos
doi:10.1038/ni.2525
Villadangos and colleagues show that lung resident memory CD8+ T cells selectively maintain expression of IFITM3, a protein that confers broad resistance to viral infection.

IL-1R signaling in dendritic cells replaces pattern-recognition receptors in promoting CD8+ T cell responses to influenza A virus   pp246 - 253
Iris K Pang, Takeshi Ichinohe and Akiko Iwasaki
doi:10.1038/ni.2514
Unlike vaccination, infection by a live pathogen often impairs dendritic cell function. Iwasaki and colleagues show that during infection with influenza virus, signaling via the IL-1 receptor is both required and sufficient for the priming of CD8+ T cells.

MHC class I-restricted myelin epitopes are cross-presented by Tip-DCs that promote determinant spreading to CD8+ T cells   pp254 - 261
Qingyong Ji, Luca Castelli and Joan M Goverman
doi:10.1038/ni.2513
Autoreactive CD8+ T cells are prevalent in multiple sclerosis. Goverman and colleagues identify tumor necrosis factor-inducible nitric oxide synthase (TNF-iNOS)-producing dendritic cells that cross-present myelin antigen to activate naive CD8+ T cells in the central nervous system.

See also: News and Views by Steinman

Distinct TCR signaling pathways drive proliferation and cytokine production in T cells   pp262 - 270
Clifford S Guy, Kate M Vignali, Jamshid Temirov, Matthew L Bettini, Abigail E Overacre, Matthew Smeltzer, Hui Zhang, Johannes B Huppa, Yu-Hwai Tsai, Camille Lobry, Jianming Xie, Peter J Dempsey, Howard C Crawford, Iannis Aifantis, Mark M Davis and Dario A A Vignali
doi:10.1038/ni.2538
Vignali and colleagues show that a full complement of ITAMs is required in the TCR-CD3 complex for TCR-driven T cell proliferation, whereas a low number of functional ITAMs is sufficient for cytokine secretion.

Mutual expression of the transcription factors Runx3 and ThPOK regulates intestinal CD4+ T cell immunity   pp271 - 280
Bernardo Sgarbi Reis, Aneta Rogoz, Frederico Azevedo Costa-Pinto, Ichiro Taniuchi and Daniel Mucida
doi:10.1038/ni.2518
CD4+ and CD8+ T cells are considered distinct functional lymphocyte subsets. Cheroutre and Mucida and their colleagues show that mature gut-associated CD4+ T cells lose ThPOK expression and reactivate CD8 cytolytic effector programs.

See also: News and Views by Anderson

Transcriptional reprogramming of mature CD4+ helper T cells generates distinct MHC class II-restricted cytotoxic T lymphocytes   pp281 - 289
Daniel Mucida, Mohammad Mushtaq Husain, Sawako Muroi, Femke van Wijk, Ryo Shinnakasu, Yoshinori Naoe, Bernardo Sgarbi Reis, Yujun Huang, Florence Lambolez, Michael Docherty, Antoine Attinger, Jr-Wen Shui, Gisen Kim, Christopher J Lena, Shinya Sakaguchi, Chizuko Miyamoto, Peng Wang, Koji Atarashi, Yunji Park, Toshinori Nakayama, Kenya Honda, Wilfried Ellmeier, Mitchell Kronenberg, Ichiro Taniuchi and Hilde Cheroutre
doi:10.1038/ni.2523
CD4+ and CD8+ T cells are considered distinct functional lymphocyte subsets. Cheroutre and Mucida and their colleagues show that mature gut-associated CD4+ T cells lose ThPOK expression and reactivate CD8 cytolytic effector programs.

See also: News and Views by Anderson

Mcl-1 is essential for the survival of plasma cells   pp290 - 297
Victor Peperzak, Ingela Vikström, Jennifer Walker, Stefan P Glaser, Melanie LePage, Christine M Coquery, Loren D Erickson, Kirsten Fairfax, Fabienne Mackay, Andreas Strasser, Stephen L Nutt and David M Tarlinton
doi:10.1038/ni.2527
Tarlinton and colleagues show that the antiapoptotic protein Mcl1 is essential for plasma cell survival and is induced by BCMA signaling in bone marrow, but not spleen, plasma cells.

Plasma cells require autophagy for sustainable immunoglobulin production   pp298 - 305
Niccolò Pengo, Maria Scolari, Laura Oliva, Enrico Milan, Federica Mainoldi, Andrea Raimondi, Claudio Fagioli, Arianna Merlini, Elisabetta Mariani, Elena Pasqualetto, Ugo Orfanelli, Maurilio Ponzoni, Roberto Sitia, Stefano Casola and Simone Cenci
doi:10.1038/ni.2524
Plasma cells are antibody 'factories', which places considerable metabolic stress on these cells. Cenci and colleagues show that long-lived plasma cells and sustained antibody production require autophagy activation.

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