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Scooped by
Gilbert C FAURE
September 17, 2016 9:56 AM
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Author Summary While numerous studies have addressed the response to primary virus infections, we know relatively little about the interplay between recurrent and/or persistent infections and the memory humoral immune response on professional...
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Scooped by
Gilbert C FAURE
September 17, 2016 5:27 AM
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Suggested by
LIGHTING
September 16, 2016 3:01 PM
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During normal and pathologic immune responses, lymph nodes can swell considerably. The lymph node vascular–stromal compartment supports and regulates the developing immune responses and undergoes dynamic expansion and remodeling. Recent studies have shown that dendritic cells (DCs), best known for their antigen presentation roles, can directly regulate the vascular–stromal compartment, pointing to a new perspective on DCs as facilitators of lymphoid tissue function. Here, we review the phases of lymph node vascular–stromal growth and remodeling during immune responses, discuss the roles of DCs, and discuss how this understanding can potentially be used for developing novel therapeutic approaches.
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Scooped by
Gilbert C FAURE
September 16, 2016 2:21 PM
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Wiskott-Aldrich syndrome (WAS) is associated with mutations in the WAS protein (WASp), which plays a critical role in the initiation of T cell receptor–driven (TCR-driven) actin polymerization.
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Scooped by
Gilbert C FAURE
September 15, 2016 1:44 PM
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Using unsupervised analysis of flow cytometry and mass cytometry data obtained from multiple mouse, macaque, and human tissues, Guilliams et al. provide a universal toolbox for the automated identification of dendritic cells. This framework represents the way forward to high-throughput and standardized analysis of dendritic cells from mutant mice and patients.
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Scooped by
Gilbert C FAURE
September 11, 2016 2:21 PM
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Scooped by
Gilbert C FAURE
September 8, 2016 2:53 PM
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Since the discovery of MHC molecules, it has taken 40 years to arrive at a coherent picture of how MHC class I and MHC class II molecules really work. This is a story of the proteases and MHC-like chaperones that support the MHC class I and II molecules in presenting peptides to the immune system. We now understand that the MHC system shapes both the repertoire of presented peptides and the subsequent T cell response, with important implications ranging from transplant rejection to tumor immunotherapies.
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Scooped by
Gilbert C FAURE
August 28, 2016 4:47 AM
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The present report meta-analyzes more than 300 empirical articles describing a relationship between psychological stress and parameters of the immune system in human participants.
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Scooped by
Gilbert C FAURE
August 25, 2016 3:51 AM
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Cellular and Molecular Immunology aims to report the dynamic progress being made in China and abroad in immunological research, and welcomes high-quality Research Articles, Reviews and Brief Reports across a broad range of topics including, but not...
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Scooped by
Gilbert C FAURE
August 24, 2016 1:57 AM
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Human Langerhans cells express CD1a, but those in mice do not, which makes determination of its function on these cells challenging in vivo. Through the use of a transgenic mouse that expresses CD1a, Winau and colleagues demonstrate that Langerhans cells use CD1a to present contact allergens and self lipid antigens and thereby worsen inflammatory skin conditions.
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Scooped by
Gilbert C FAURE
August 23, 2016 7:38 AM
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Scooped by
Gilbert C FAURE
August 23, 2016 3:29 AM
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Rare and sometimes lethal disease affects young children
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Suggested by
LIGHTING
August 22, 2016 3:18 PM
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Calabro et al. demonstrate that, upon immunization, dendritic cell subsets in the spleen migrate into non-overlapping zones that correspond to regions enriched for CD4+ or CD8+ T cells. This differential migration results in the selective induction of either CD4+ or CD8+ T cell responses.
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Scooped by
Gilbert C FAURE
September 17, 2016 9:53 AM
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Influenza still remains a current concern. To be prepared for the next outbreak the understanding of viral mechanisms, host-pathogen interactions and immunological pathways is essential.
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Suggested by
LIGHTING
September 16, 2016 3:01 PM
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A generation ago, the immunoglobulin intramolecular signaling, or allosteric, hypothesis was abandoned in favor of the associative hypothesis, which posited that Fc receptor crosslinking produced the increased affinity of antigen–antibody complexes. This essay argues that there is sufficient evidence to resuscitate the allosteric hypothesis, at least for some antibodies.
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Scooped by
Gilbert C FAURE
September 16, 2016 2:24 PM
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Clinical & Translational Immunology <br/><br/><br/>Innate immune cells have a critical role in defense against infection and disease.
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Scooped by
Gilbert C FAURE
September 15, 2016 1:46 PM
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The formation of germinal center B cells is crucial to the production of high-affinity antibodies during the humoral immune response. Here, Bunting et al. provide evidence for multilayered reorganization of genomic architecture centered around BCL6 and an upstream locus control region, coordinating the transcriptional reprograming during the transition between naive and germinal center B cells.
We all produce as many as 100,000 different types of cancer cells every day, which are recognized and eliminated by our extraordinarily efficient immune system.
Via Krishan Maggon
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Scooped by
Gilbert C FAURE
September 8, 2016 2:56 PM
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The New England Journal of Medicine
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Suggested by
LIGHTING
September 8, 2016 1:59 PM
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Scooped by
Gilbert C FAURE
August 25, 2016 3:52 AM
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Background and Aim Hepatitis B virus-related acute-on-chronic liver failure (HBV-ACLF) is an acute deterioration of liver function on chronic liver disease with immune disorder.
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Scooped by
Gilbert C FAURE
August 24, 2016 9:56 AM
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ABSTRACT Cytokine-induced neutrophil mobilization from the bone marrow to circulation is a critical event in acute inflammation, but how it is accurately controlled remains poorly understood. In this study, we report that CXCR2 ligands are responsible for rapid neutrophil mobilization during early-stage acute inflammation. Nevertheless, although serum CXCR2 ligand concentrations increased during inflammation, neutrophil mobilization slowed after an initial acute fast phase, suggesting a suppression of neutrophil response to CXCR2 ligands after the acute phase. We demonstrate that granulocyte colony-stimulating factor (G-CSF), usually considered a prototypical neutrophil-mobilizing cytokine, was expressed later in the acute inflammatory response and unexpectedly impeded CXCR2-induced neutrophil mobilization by negatively regulating CXCR2-mediated intracellular signaling. Blocking G-CSF in vivo paradoxically elevated peripheral blood neutrophil counts in mice injected intraperitoneally with Escherichia coli and sequestered large numbers of neutrophils in the lungs, leading to sterile pulmonary inflammation. In a lipopolysaccharide-induced acute lung injury model, the homeostatic imbalance caused by G-CSF blockade enhanced neutrophil accumulation, edema, and inflammation in the lungs and ultimately led to significant lung damage. Thus, physiologically produced G-CSF not only acts as a neutrophil mobilizer at the relatively late stage of acute inflammation, but also prevents exaggerated neutrophil mobilization and the associated inflammation-induced tissue damage during early-phase infection and inflammation. Submitted: 16 March 2016
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Scooped by
Gilbert C FAURE
August 24, 2016 1:57 AM
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The immune system tailors its responses according to the level of threat. Lemaitre and colleagues identify a novel version of the peptidoglycan receptor PGRP-LC and demonstrate that it tunes immune responses to live (threatening) or dead (harmless) bacteria.
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Scooped by
Gilbert C FAURE
August 23, 2016 3:30 AM
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Similarly to cars, cells need a steering mechanism that guides them towards a certain target or direction. Scientists at the Center for Cognition and Sociality (Institute for Basic Science, IBS), and KAIST, led by Prof.
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Scooped by
Gilbert C FAURE
August 23, 2016 3:20 AM
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Researchers use new experimental models and analytical tools to investigate genes regulated by Foxn1, becoming the first to identify the DNA sequence bound by the transcription factor.
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