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 inFrontiers in immunology Vol. 14; p. 1199422
Main Authors Gail, Laura Marie, Schell, Kimberly Julia, Łacina, Piotr, Strobl, Johanna, Bolton, Steven J, Steinbakk Ulriksen, Emilie, Bogunia-Kubik, Katarzyna, Greinix, Hildegard, Crossland, Rachel Emily, Inngjerdingen, Marit, Stary, Georg
Format Journal Article
LanguageEnglish
Published Switzerland 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.
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
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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
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ObjectType-Review-1
Edited by: Tomomi Toubai, Yamagata University, Japan
Reviewed by: Federico Simonetta, Hôpitaux universitaires de Genève (HUG), Switzerland; Hideaki Fujiwara, Okayama University, Japan; Shuichiro Takahashi, Fred Hutchinson Cancer Research Center, United States
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332803/
PMID 37435079
PQID 2836293936
PQPubID 23479
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PublicationCentury 2000
PublicationDate 2023-06-26
PublicationDateYYYYMMDD 2023-06-26
PublicationDate_xml – month: 06
  year: 2023
  text: 2023-06-26
  day: 26
PublicationDecade 2020
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
PublicationTitle Frontiers in immunology
PublicationTitleAlternate Front Immunol
PublicationYear 2023
Publisher Frontiers Media S.A
Publisher_xml – name: Frontiers Media S.A
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Snippet Chronic Graft-versus-Host Disease is a life-threatening inflammatory condition that affects many patients after allogeneic hematopoietic stem cell...
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StartPage 1199422
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
URI https://www.ncbi.nlm.nih.gov/pubmed/37435079
https://search.proquest.com/docview/2836293936
https://pubmed.ncbi.nlm.nih.gov/PMC10332803
https://doaj.org/article/fb995d204e5e4efd9c33469da1e33256
Volume 14
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