Complex interactions of cellular players in chronic Graft-versus-Host Disease
Chronic Graft-versus-Host Disease is a life-threatening inflammatory condition that affects many patients after allogeneic hematopoietic stem cell transplantation. Although we have made substantial progress in understanding disease pathogenesis and the role of specific immune cell subsets, treatment...
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Published in | Frontiers in immunology Vol. 14; p. 1199422 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Frontiers Media S.A
26.06.2023
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Abstract | Chronic Graft-versus-Host Disease is a life-threatening inflammatory condition that affects many patients after allogeneic hematopoietic stem cell transplantation. Although we have made substantial progress in understanding disease pathogenesis and the role of specific immune cell subsets, treatment options are still limited. To date, we lack a global understanding of the interplay between the different cellular players involved, in the affected tissues and at different stages of disease development and progression. In this review we summarize our current knowledge on pathogenic and protective mechanisms elicited by the major involved immune subsets, being T cells, B cells, NK cells and antigen presenting cells, as well as the microbiome, with a special focus on intercellular communication of these cell types
extracellular vesicles as up-and-coming fields in chronic Graft-versus-Host Disease research. Lastly, we discuss the importance of understanding systemic and local aberrant cell communication during disease for defining better biomarkers and therapeutic targets, eventually enabling the design of personalized treatment schemes. |
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AbstractList | Chronic Graft-versus-Host Disease is a life-threatening inflammatory condition that affects many patients after allogeneic hematopoietic stem cell transplantation. Although we have made substantial progress in understanding disease pathogenesis and the role of specific immune cell subsets, treatment options are still limited. To date, we lack a global understanding of the interplay between the different cellular players involved, in the affected tissues and at different stages of disease development and progression. In this review we summarize our current knowledge on pathogenic and protective mechanisms elicited by the major involved immune subsets, being T cells, B cells, NK cells and antigen presenting cells, as well as the microbiome, with a special focus on intercellular communication of these cell types
via
extracellular vesicles as up-and-coming fields in chronic Graft-versus-Host Disease research. Lastly, we discuss the importance of understanding systemic and local aberrant cell communication during disease for defining better biomarkers and therapeutic targets, eventually enabling the design of personalized treatment schemes. Chronic Graft-versus-Host Disease is a life-threatening inflammatory condition that affects many patients after allogeneic hematopoietic stem cell transplantation. Although we have made substantial progress in understanding disease pathogenesis and the role of specific immune cell subsets, treatment options are still limited. To date, we lack a global understanding of the interplay between the different cellular players involved, in the affected tissues and at different stages of disease development and progression. In this review we summarize our current knowledge on pathogenic and protective mechanisms elicited by the major involved immune subsets, being T cells, B cells, NK cells and antigen presenting cells, as well as the microbiome, with a special focus on intercellular communication of these cell types via extracellular vesicles as up-and-coming fields in chronic Graft-versus-Host Disease research. Lastly, we discuss the importance of understanding systemic and local aberrant cell communication during disease for defining better biomarkers and therapeutic targets, eventually enabling the design of personalized treatment schemes. Chronic Graft-versus-Host Disease is a life-threatening inflammatory condition that affects many patients after allogeneic hematopoietic stem cell transplantation. Although we have made substantial progress in understanding disease pathogenesis and the role of specific immune cell subsets, treatment options are still limited. To date, we lack a global understanding of the interplay between the different cellular players involved, in the affected tissues and at different stages of disease development and progression. In this review we summarize our current knowledge on pathogenic and protective mechanisms elicited by the major involved immune subsets, being T cells, B cells, NK cells and antigen presenting cells, as well as the microbiome, with a special focus on intercellular communication of these cell types extracellular vesicles as up-and-coming fields in chronic Graft-versus-Host Disease research. Lastly, we discuss the importance of understanding systemic and local aberrant cell communication during disease for defining better biomarkers and therapeutic targets, eventually enabling the design of personalized treatment schemes. |
Author | Inngjerdingen, Marit Stary, Georg Greinix, Hildegard Strobl, Johanna Steinbakk Ulriksen, Emilie Schell, Kimberly Julia Gail, Laura Marie Łacina, Piotr Bolton, Steven J Bogunia-Kubik, Katarzyna Crossland, Rachel Emily |
AuthorAffiliation | 5 Department of Pharmacology, Oslo University Hospital , Oslo , Norway 4 Laboratory of Clinical Immunogenetics and Pharmacogenetics, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences , Wrocław , Poland 1 Department of Dermatology, Medical University of Vienna , Vienna , Austria 3 Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University , Newcastle upon Tyne , United Kingdom 6 Department of Internal Medicine, Division of Hematology, Medical University of Graz , Graz , Austria 2 CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences , Vienna , Austria |
AuthorAffiliation_xml | – name: 5 Department of Pharmacology, Oslo University Hospital , Oslo , Norway – name: 1 Department of Dermatology, Medical University of Vienna , Vienna , Austria – name: 3 Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University , Newcastle upon Tyne , United Kingdom – name: 2 CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences , Vienna , Austria – name: 4 Laboratory of Clinical Immunogenetics and Pharmacogenetics, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences , Wrocław , Poland – name: 6 Department of Internal Medicine, Division of Hematology, Medical University of Graz , Graz , Austria |
Author_xml | – sequence: 1 givenname: Laura Marie surname: Gail fullname: Gail, Laura Marie organization: CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria – sequence: 2 givenname: Kimberly Julia surname: Schell fullname: Schell, Kimberly Julia organization: Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom – sequence: 3 givenname: Piotr surname: Łacina fullname: Łacina, Piotr organization: Laboratory of Clinical Immunogenetics and Pharmacogenetics, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland – sequence: 4 givenname: Johanna surname: Strobl fullname: Strobl, Johanna organization: CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria – sequence: 5 givenname: Steven J surname: Bolton fullname: Bolton, Steven J organization: Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom – sequence: 6 givenname: Emilie surname: Steinbakk Ulriksen fullname: Steinbakk Ulriksen, Emilie organization: Department of Pharmacology, Oslo University Hospital, Oslo, Norway – sequence: 7 givenname: Katarzyna surname: Bogunia-Kubik fullname: Bogunia-Kubik, Katarzyna organization: Laboratory of Clinical Immunogenetics and Pharmacogenetics, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland – sequence: 8 givenname: Hildegard surname: Greinix fullname: Greinix, Hildegard organization: Department of Internal Medicine, Division of Hematology, Medical University of Graz, Graz, Austria – sequence: 9 givenname: Rachel Emily surname: Crossland fullname: Crossland, Rachel Emily organization: Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom – sequence: 10 givenname: Marit surname: Inngjerdingen fullname: Inngjerdingen, Marit organization: Department of Pharmacology, Oslo University Hospital, Oslo, Norway – sequence: 11 givenname: Georg surname: Stary fullname: Stary, Georg organization: CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37435079$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_blre_2023_101141 crossref_primary_10_1016_j_biopha_2024_116652 crossref_primary_10_3389_fimmu_2024_1358668 crossref_primary_10_3390_cells13030213 |
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Copyright | Copyright © 2023 Gail, Schell, Łacina, Strobl, Bolton, Steinbakk Ulriksen, Bogunia-Kubik, Greinix, Crossland, Inngjerdingen and Stary. Copyright © 2023 Gail, Schell, Łacina, Strobl, Bolton, Steinbakk Ulriksen, Bogunia-Kubik, Greinix, Crossland, Inngjerdingen and Stary 2023 Gail, Schell, Łacina, Strobl, Bolton, Steinbakk Ulriksen, Bogunia-Kubik, Greinix, Crossland, Inngjerdingen and Stary |
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Keywords | hematopoietic stem cell transplantation immune cell networks GvHD pathogenesis cell-cell communication chronic graft-versus-host disease |
Language | English |
License | Copyright © 2023 Gail, Schell, Łacina, Strobl, Bolton, Steinbakk Ulriksen, Bogunia-Kubik, Greinix, Crossland, Inngjerdingen and Stary. 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. |
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SubjectTerms | Antigen-Presenting Cells B-Lymphocytes Bronchiolitis Obliterans Syndrome Cell Communication cell-cell communication chronic graft-versus-host disease Extracellular Vesicles GvHD pathogenesis hematopoietic stem cell transplantation Humans immune cell networks Immunology |
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Title | Complex interactions of cellular players in chronic Graft-versus-Host Disease |
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