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      Cellular activation pathways and interaction networks in vascularized composite allotransplantation

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          Abstract

          Vascularized composite allotransplantation (VCA) is an evolving field of reconstructive surgery that has revolutionized the treatment of patients with devastating injuries, including those with limb losses or facial disfigurement. The transplanted units are typically comprised of different tissue types, including skin, mucosa, blood and lymphatic vasculature, muscle, and bone. It is widely accepted that the antigenicity of some VCA components, such as skin, is particularly potent in eliciting a strong recipient rejection response following transplantation. The fine line between tolerance and rejection of the graft is orchestrated by different cell types, including both donor and recipient-derived lymphocytes, macrophages, and other immune and donor-derived tissue cells (e.g., endothelium). Here, we delineate the role of different cell and tissue types during VCA rejection. Rejection of VCA grafts and the necessity of life-long multidrug immunosuppression remains one of the major challenges in this field. This review sheds light on recent developments in decoding the cellular signature of graft rejection in VCA and how these may, ultimately, influence the clinical management of VCA patients by way of novel therapies that target specific cellular processes.

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          Most cited references214

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          How regulatory T cells work.

          Regulatory T (T(Reg)) cells are essential for maintaining peripheral tolerance, preventing autoimmune diseases and limiting chronic inflammatory diseases. However, they also limit beneficial responses by suppressing sterilizing immunity and limiting antitumour immunity. Given that T(Reg) cells can have both beneficial and deleterious effects, there is considerable interest in determining their mechanisms of action. In this Review, we describe the basic mechanisms used by T(Reg) cells to mediate suppression and discuss whether one or many of these mechanisms are likely to be crucial for T(Reg)-cell function. In addition, we propose the hypothesis that effector T cells may not be 'innocent' parties in this suppressive process and might in fact potentiate T(Reg)-cell function.
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            Mechanisms of clathrin-mediated endocytosis

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              Tissue-resident macrophages.

              Tissue-resident macrophages are a heterogeneous population of immune cells that fulfill tissue-specific and niche-specific functions. These range from dedicated homeostatic functions, such as clearance of cellular debris and iron processing, to central roles in tissue immune surveillance, response to infection and the resolution of inflammation. Recent studies highlight marked heterogeneity in the origins of tissue macrophages that arise from hematopoietic versus self-renewing embryo-derived populations. We discuss the tissue niche-specific factors that dictate cell phenotype, the definition of which will allow new strategies to promote the restoration of tissue homeostasis. Understanding the mechanisms that dictate tissue macrophage heterogeneity should explain why simplified models of macrophage activation do not explain the extent of heterogeneity seen in vivo.
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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
                17 May 2023
                2023
                : 14
                : 1179355
                Affiliations
                [1] 1 Department of Plastic, Hand and Reconstructive Surgery, University Hospital Regensburg , Regensburg, Germany
                [2] 2 Division of Plastic Surgery, Department of Surgery, Yale New Haven Hospital, Yale School of Medicine , New Haven, CT, United States
                [3] 3 Department of Surgery, Division of Plastic Surgery, Brigham and Women’s Hospital, Harvard Medical School , Boston, MA, United States
                [4] 4 Department of Hand, Plastic and Reconstructive Surgery, Microsurgery, Burn Center, BG Trauma Center Ludwigshafen, University of Heidelberg , Ludwigshafen, Germany
                [5] 5 Department of Pathology, Brigham and Women’s Hospital , Boston, MA, United States
                [6] 6 Department of Plastic, Aesthetic, Hand and Reconstructive Surgery, Burn Center, Hannover Medical School , Hannover, Germany
                [7] 7 Division of Transplant Surgery, Department of Surgery, Brigham and Women’s Hospital, Harvard Medical School , Boston, MA, United States
                [8] 8 Department of Plastic Surgery, Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health , Berlin, Germany
                Author notes

                Edited by: Malgorzata Kloc, Houston Methodist Research Institute, United States

                Reviewed by: Philippe Lemaitre, Columbia University, United States; Sara Shamdani, Hôpital Paul Brousse, France

                *Correspondence: Martin Kauke-Navarro, kauke-navarro.martin@ 123456yale.edu ; Leonard Knoedler, Leonard.Knoedler@ 123456ur.de

                †These authors have contributed equally to this work

                Article
                10.3389/fimmu.2023.1179355
                10230044
                37266446
                c4683e9c-8361-4e82-8f87-4c9d3c8126d5
                Copyright © 2023 Knoedler, Knoedler, Panayi, Lee, Sadigh, Huelsboemer, Stoegner, Schroeter, Kern, Mookerjee, Lian, Tullius, Murphy, Pomahac and Kauke-Navarro

                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
                : 04 March 2023
                : 28 April 2023
                Page count
                Figures: 3, Tables: 1, Equations: 0, References: 215, Pages: 20, Words: 11052
                Categories
                Immunology
                Review
                Custom metadata
                Alloimmunity and Transplantation

                Immunology
                transplant,reconstructive surgery,vascularized composite allotransplantation,vca,alloimmune response,acute rejection,chronic rejection

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