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      Current Concepts on 6-sulfo LacNAc Expressing Monocytes (slanMo)

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          Abstract

          The human mononuclear phagocytes system consists of dendritic cells (DCs), monocytes, and macrophages having different functions in bridging innate and adaptive immunity. Among the heterogeneous population of monocytes the cell surface marker slan (6-sulfo LacNAc) identifies a specific subset of human CD14 CD16 + non-classical monocytes, called slan + monocytes (slanMo). In this review we discuss the identity and functions of slanMo, their contributions to immune surveillance by pro-inflammatory cytokine production, and cross talk with T cells and NK cells. We also consider the role of slanMo in the regulation of chronic inflammatory diseases and cancer. Finally, we highlight unresolved questions that should be the focus of future research.

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          Taking dendritic cells into medicine.

          Dendritic cells (DCs) orchestrate a repertoire of immune responses that bring about resistance to infection and silencing or tolerance to self. In the settings of infection and cancer, microbes and tumours can exploit DCs to evade immunity, but DCs also can generate resistance, a capacity that is readily enhanced with DC-targeted vaccines. During allergy, autoimmunity and transplant rejection, DCs instigate unwanted responses that cause disease, but, again, DCs can be harnessed to silence these conditions with novel therapies. Here we present some medical implications of DC biology that account for illness and provide opportunities for prevention and therapy.
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            The fate and lifespan of human monocyte subsets in steady state and systemic inflammation

            Using stable isotope labeling, Patel et al. establish the lifespan of all three human monocyte subsets that circulate in dynamic equilibrium; in steady state, classical monocytes are short-lived precursors with the potential to become intermediate and nonclassical monocytes. They highlight that systemic inflammation induces an emergency release of classical monocytes into the circulation.
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              IL-17 family cytokines and the expanding diversity of effector T cell lineages.

              Since its conception two decades ago, the Th1-Th2 paradigm has provided a framework for understanding T cell biology and the interplay of innate and adaptive immunity. Naive T cells differentiate into effector T cells with enhanced functional potential for orchestrating pathogen clearance largely under the guidance of cytokines produced by cells of the innate immune system that have been activated by recognition of those pathogens. This secondary education of post-thymic T cells provides a mechanism for appropriately matching adaptive immunity to frontline cues of the innate immune system. Owing in part to the rapid identification of novel cytokines of the IL-17 and IL-12 families using database searches, the factors that specify differentiation of a new effector T cell lineage-Th17-have now been identified, providing a new arm of adaptive immunity and presenting a unifying model that can explain many heretofore confusing aspects of immune regulation, immune pathogenesis, and host defense.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                22 May 2019
                2019
                : 10
                : 948
                Affiliations
                [1] 1Department of Dermatology, Heidelberg University Hospital , Heidelberg, Germany
                [2] 2Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases , Bethesda, MD, United States
                [3] 3Institute of Immunology, Faculty of Medicine Carl Gustav Carus, Technische Universtät Dresden , Dresden, Germany
                [4] 4Partner Site Dresden, National Center for Tumor Diseases (NCT) , Dresden, Germany
                Author notes

                Edited by: Silvia Beatriz Boscardin, University of São Paulo, Brazil

                Reviewed by: Elizabeth Mellins, Stanford University, United States; Pieter J. M. Leenen, Erasmus University Rotterdam, Netherlands

                *Correspondence: Knut Schäkel knut.schaekel@ 123456med.uni-heidelberg.de

                This article was submitted to Antigen Presenting Cell Biology, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2019.00948
                6540605
                31191513
                129ab9b1-b9b0-423f-939f-7e412ca9f69d
                Copyright © 2019 Ahmad, Döbel, Schmitz and Schäkel.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 15 October 2018
                : 12 April 2019
                Page count
                Figures: 2, Tables: 2, Equations: 0, References: 133, Pages: 13, Words: 10805
                Categories
                Immunology
                Review

                Immunology
                slan+ monocytes,slanmo,non-classical monocytes,inflammation,autoimmunity,cancer,infection,psoriasis
                Immunology
                slan+ monocytes, slanmo, non-classical monocytes, inflammation, autoimmunity, cancer, infection, psoriasis

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