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      Current Preventions and Treatments of aGVHD: From Pharmacological Prophylaxis to Innovative Therapies

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          Abstract

          Graft versus host disease (GVHD) is one of the main causes of mortality and the reason for up to 50% of morbidity after hematopoietic stem cell transplantations (HSCT) which is the treatment of choice for many blood malignancies. Thanks to years of research and exploration, we have acquired a profound understanding of the pathophysiology and immunopathology of these disorders. This led to the proposition and development of many therapeutic approaches during the last decades, some of them with very promising results. In this review, we have focused on the recent GVHD treatments from classical chemical and pharmacological prophylaxis to more innovative treatments including gene therapy and cell therapy, most commonly based on the application of a variety of immunomodulatory cells. Furthermore, we have discussed the advantages and potentials of cell-free therapy as a newly emerging approach to treat GVHD. Among them, we have particularly focused on the implication of the TNFα-TNFR2 axis as a new immune checkpoint signaling pathway controlling different aspects of many immunoregulatory cells.

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          Most cited references200

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          Multilineage potential of adult human mesenchymal stem cells.

          Human mesenchymal stem cells are thought to be multipotent cells, which are present in adult marrow, that can replicate as undifferentiated cells and that have the potential to differentiate to lineages of mesenchymal tissues, including bone, cartilage, fat, tendon, muscle, and marrow stroma. Cells that have the characteristics of human mesenchymal stem cells were isolated from marrow aspirates of volunteer donors. These cells displayed a stable phenotype and remained as a monolayer in vitro. These adult stem cells could be induced to differentiate exclusively into the adipocytic, chondrocytic, or osteocytic lineages. Individual stem cells were identified that, when expanded to colonies, retained their multilineage potential.
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            Exosomes: composition, biogenesis and function

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              Graft-versus-host disease.

              Haemopoietic-cell transplantation (HCT) is an intensive therapy used to treat high-risk haematological malignant disorders and other life-threatening haematological and genetic diseases. The main complication of HCT is graft-versus-host disease (GVHD), an immunological disorder that affects many organ systems, including the gastrointestinal tract, liver, skin, and lungs. The number of patients with this complication continues to grow, and many return home from transplant centres after HCT requiring continued treatment with immunosuppressive drugs that increases their risks for serious infections and other complications. In this Seminar, we review our understanding of the risk factors and causes of GHVD, the cellular and cytokine networks implicated in its pathophysiology, and current strategies to prevent and treat the disease. We also summarise supportive-care measures that are essential for management of this medically fragile population.
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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 December 2020
                2020
                17 December 2020
                : 11
                : 607030
                Affiliations
                [1] 1INSERM UMR-S-MD 1197, Hôpital Paul Brousse , Villejuif, France
                [2] 2Paris-Saclay University , Villejuif, France
                [3] 3CellMedEx , Saint Maur Des Fossés, France
                [4] 4Service d’Hématologie Clinique et de Thérapie Cellulaire, Hôpital Henri Mondor , Créteil, France
                [5] 5INSERM U955, Institut Mondor de Recherche Biomédicale , Créteil, France
                [6] 6Faculté de Médecine de Créteil, Université Paris-Est , Créteil, France
                Author notes

                Edited by: Michaela Lucas, University of Western Australia, Australia

                Reviewed by: Luca Castagna, Humanitas Research Hospital, Italy; Guido Moll, Charité-Universitätsmedizin Berlin, Germany

                This article was submitted to Alloimmunity and Transplantation, a section of the journal Frontiers in Immunology

                †These authors have contributed equally to this work

                Article
                10.3389/fimmu.2020.607030
                7773902
                33391276
                53e41ec2-485e-457d-8fdc-3a84a01b5004
                Copyright © 2020 Naserian, Leclerc, Shamdani and Uzan

                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
                : 16 September 2020
                : 16 November 2020
                Page count
                Figures: 2, Tables: 0, Equations: 0, References: 202, Pages: 15, Words: 6957
                Funding
                Funded by: Agence Nationale de la Recherche 10.13039/501100001665
                Categories
                Immunology
                Review

                Immunology
                hematopoietic stem cell transplantation,graft versus host disease,t cells,immunoregulation,tolerance induction,cell therapy,tnfα-tnfr2 signaling pathway

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