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      Role of Mast Cells and Type 2 Innate Lymphoid (ILC2) Cells in Lung Transplantation

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          Abstract

          The multifunctional role of mast cells (MCs) in the immune system is complex and has not fully been explored. MCs reside in tissues and mucous membranes such as the lung, digestive tract, and skin which are strategically located at interfaces with the external environment. These cells, therefore, will encounter external stimuli and pathogens. MCs modulate both the innate and the adaptive immune response in inflammatory disorders including transplantation. MCs can have pro- and anti-inflammatory functions, thereby regulating the outcome of lung transplantation through secretion of mediators that allow interaction with other cell types, particularly innate lymphoid cells (ILC2). ILC2 cells are a unique population of hematopoietic cells that coordinate the innate immune response against a variety of threats including infection, tissue damage, and homeostatic disruption. In addition, MCs can modulate alloreactive T cell responses or assist in T regulatory (Treg) cell activity. This paper outlines the current understanding of the role of MCs in lung transplantation, with a specific focus on their interaction with ILC2 cells within the engrafted organ.

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          Most cited references99

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          Innate lymphoid cells promote lung-tissue homeostasis after infection with influenza virus

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            Type 2 immunity in tissue repair and fibrosis

            In this Review, the authors describe how type 2 immune responses drive tissue repair and fibrosis. They explain how these responses are crucial for repairing damaged tissue but can also lead to pathological outcomes if not properly regulated.
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              Multi-organ, multi-lineage engraftment by a single bone marrow-derived stem cell.

              Purification of rare hematopoietic stem cell(s) (HSC) to homogeneity is required to study their self-renewal, differentiation, phenotype, and homing. Long-term repopulation (LTR) of irradiated hosts and serial transplantation to secondary hosts represent the gold standard for demonstrating self-renewal and differentiation, the defining properties of HSC. We show that rare cells that home to bone marrow can LTR primary and secondary recipients. During the homing, CD34 and SCA-1 expression increases uniquely on cells that home to marrow. These adult bone marrow cells have tremendous differentiative capacity as they can also differentiate into epithelial cells of the liver, lung, GI tract, and skin. This finding may contribute to clinical treatment of genetic disease or tissue repair.
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                Author and article information

                Contributors
                Journal
                J Immunol Res
                J Immunol Res
                JIR
                Journal of Immunology Research
                Hindawi
                2314-8861
                2314-7156
                2018
                30 October 2018
                : 2018
                : 2785971
                Affiliations
                1Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran
                2Department of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
                3Cell and Molecular Biology Group, Airways Disease Section, National Heart and Lung Institute, Imperial College London, Dovehouse Street, London, UK
                4Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute, The University of Newcastle, Newcastle, New South Wales, Australia
                5Division of Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Faculty of Science, Utrecht University, Utrecht, Netherlands
                6Department of Pulmonary Medicine, Erasmus MC, Rotterdam, Netherlands
                7Nutricia Research, Immunology, Utrecht, Netherlands
                Author notes

                Guest Editor: Laurent L. Reber

                Author information
                http://orcid.org/0000-0002-7753-9624
                http://orcid.org/0000-0003-2101-8843
                http://orcid.org/0000-0003-0630-2192
                Article
                10.1155/2018/2785971
                6232810
                30510964
                de35db6a-d77e-40bb-b1bc-e7548db4e042
                Copyright © 2018 Esmaeil Mortaz et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 April 2018
                : 10 August 2018
                : 14 September 2018
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