Potential of glycosylation research in graft versus host disease after allogeneic hematopoietic stem cell transplantation
Glycans, complex oligosaccharides, are directly involved in almost every biological process, have a fundamental role in the immune system, and are probably involved in nearly every human disease. However, glycosylation has been greatly ignored in the area of allogeneic hematopoietic stem cell transp...
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| Published in | Biochimica et biophysica acta Vol. 1860; no. 8; pp. 1615 - 1622 |
|---|---|
| Main Authors | , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Netherlands
Elsevier B.V
01.08.2016
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0304-4165 0006-3002 1872-8006 |
| DOI | 10.1016/j.bbagen.2016.02.015 |
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| Abstract | Glycans, complex oligosaccharides, are directly involved in almost every biological process, have a fundamental role in the immune system, and are probably involved in nearly every human disease. However, glycosylation has been greatly ignored in the area of allogeneic hematopoietic stem cell transplantation (alloHSCT) and graft versus host disease (GVHD). Both acute and chronic GVHD are multisystemic debilitating immunological disturbances arising after alloHSCT.
In this paper, we review the glycosylation research already done in the field of alloHSCT and GVHD and evaluate further potential of glycan analysis in GVHD by looking into resembling inflammatory and autoimmune conditions.
Glycan research could bring significant improvement in alloHSCT procedure with reduction in following complications, such as GVHD. Identifying glycan patterns that induce self-tolerance and the ones that cause the auto- and allo-immune response could lead to innovative and tissue-specific immunomodulative therapy instead of the current immunosuppressive treatment, enabling preservation of the graft-versus-tumor effect. Moreover, improved glycan pattern analyses could offer a more complete assessment and greatly needed dynamic biomarkers for GVHD.
This review is written with a goal to encourage glycan research in the field of alloHSCT and GVHD as a perspective tool leading to improved engraftment, discovery of much needed biomarkers for GVHD, enabling an appropriate therapy and improved monitoring of therapeutic response. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc.
•Glycans are involved in almost every biological process.•Glycans are associated with immunological disturbances and autoimmune diseases.•GVHD is alloimmune and autoimmune disorder following alloHSCT.•Glycans have a great research potential in clarifying events after alloHSCT and GVHD.•Glycan research could lead to improved therapy and discovery of biomarkers. |
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| AbstractList | Glycans, complex oligosaccharides, are directly involved in almost every biological process, have a fundamental role in the immune system, and are probably involved in nearly every human disease. However, glycosylation has been greatly ignored in the area of allogeneic hematopoietic stem cell transplantation (alloHSCT) and graft versus host disease (GVHD). Both acute and chronic GVHD are multisystemic debilitating immunological disturbances arising after alloHSCT.BACKGROUNDGlycans, complex oligosaccharides, are directly involved in almost every biological process, have a fundamental role in the immune system, and are probably involved in nearly every human disease. However, glycosylation has been greatly ignored in the area of allogeneic hematopoietic stem cell transplantation (alloHSCT) and graft versus host disease (GVHD). Both acute and chronic GVHD are multisystemic debilitating immunological disturbances arising after alloHSCT.In this paper, we review the glycosylation research already done in the field of alloHSCT and GVHD and evaluate further potential of glycan analysis in GVHD by looking into resembling inflammatory and autoimmune conditions.SCOPE OF REVIEWIn this paper, we review the glycosylation research already done in the field of alloHSCT and GVHD and evaluate further potential of glycan analysis in GVHD by looking into resembling inflammatory and autoimmune conditions.Glycan research could bring significant improvement in alloHSCT procedure with reduction in following complications, such as GVHD. Identifying glycan patterns that induce self-tolerance and the ones that cause the auto- and allo-immune response could lead to innovative and tissue-specific immunomodulative therapy instead of the current immunosuppressive treatment, enabling preservation of the graft-versus-tumor effect. Moreover, improved glycan pattern analyses could offer a more complete assessment and greatly needed dynamic biomarkers for GVHD.MAJOR CONCLUSIONSGlycan research could bring significant improvement in alloHSCT procedure with reduction in following complications, such as GVHD. Identifying glycan patterns that induce self-tolerance and the ones that cause the auto- and allo-immune response could lead to innovative and tissue-specific immunomodulative therapy instead of the current immunosuppressive treatment, enabling preservation of the graft-versus-tumor effect. Moreover, improved glycan pattern analyses could offer a more complete assessment and greatly needed dynamic biomarkers for GVHD.This review is written with a goal to encourage glycan research in the field of alloHSCT and GVHD as a perspective tool leading to improved engraftment, discovery of much needed biomarkers for GVHD, enabling an appropriate therapy and improved monitoring of therapeutic response. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc.GENERAL SIGNIFICANCEThis review is written with a goal to encourage glycan research in the field of alloHSCT and GVHD as a perspective tool leading to improved engraftment, discovery of much needed biomarkers for GVHD, enabling an appropriate therapy and improved monitoring of therapeutic response. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc. Glycans, complex oligosaccharides, are directly involved in almost every biological process, have a fundamental role in the immune system, and are probably involved in nearly every human disease. However, glycosylation has been greatly ignored in the area of allogeneic hematopoietic stem cell transplantation (alloHSCT) and graft versus host disease (GVHD). Both acute and chronic GVHD are multisystemic debilitating immunological disturbances arising after alloHSCT. In this paper, we review the glycosylation research already done in the field of alloHSCT and GVHD and evaluate further potential of glycan analysis in GVHD by looking into resembling inflammatory and autoimmune conditions. Glycan research could bring significant improvement in alloHSCT procedure with reduction in following complications, such as GVHD. Identifying glycan patterns that induce self-tolerance and the ones that cause the auto- and allo-immune response could lead to innovative and tissue-specific immunomodulative therapy instead of the current immunosuppressive treatment, enabling preservation of the graft-versus-tumor effect. Moreover, improved glycan pattern analyses could offer a more complete assessment and greatly needed dynamic biomarkers for GVHD. This review is written with a goal to encourage glycan research in the field of alloHSCT and GVHD as a perspective tool leading to improved engraftment, discovery of much needed biomarkers for GVHD, enabling an appropriate therapy and improved monitoring of therapeutic response. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc. Glycans, complex oligosaccharides, are directly involved in almost every biological process, have a fundamental role in the immune system, and are probably involved in nearly every human disease. However, glycosylation has been greatly ignored in the area of allogeneic hematopoietic stem cell transplantation (alloHSCT) and graft versus host disease (GVHD). Both acute and chronic GVHD are multisystemic debilitating immunological disturbances arising after alloHSCT.In this paper, we review the glycosylation research already done in the field of alloHSCT and GVHD and evaluate further potential of glycan analysis in GVHD by looking into resembling inflammatory and autoimmune conditions.Glycan research could bring significant improvement in alloHSCT procedure with reduction in following complications, such as GVHD. Identifying glycan patterns that induce self-tolerance and the ones that cause the auto- and allo-immune response could lead to innovative and tissue-specific immunomodulative therapy instead of the current immunosuppressive treatment, enabling preservation of the graft-versus-tumor effect. Moreover, improved glycan pattern analyses could offer a more complete assessment and greatly needed dynamic biomarkers for GVHD.This review is written with a goal to encourage glycan research in the field of alloHSCT and GVHD as a perspective tool leading to improved engraftment, discovery of much needed biomarkers for GVHD, enabling an appropriate therapy and improved monitoring of therapeutic response. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc. Glycans, complex oligosaccharides, are directly involved in almost every biological process, have a fundamental role in the immune system, and are probably involved in nearly every human disease. However, glycosylation has been greatly ignored in the area of allogeneic hematopoietic stem cell transplantation (alloHSCT) and graft versus host disease (GVHD). Both acute and chronic GVHD are multisystemic debilitating immunological disturbances arising after alloHSCT. In this paper, we review the glycosylation research already done in the field of alloHSCT and GVHD and evaluate further potential of glycan analysis in GVHD by looking into resembling inflammatory and autoimmune conditions. Glycan research could bring significant improvement in alloHSCT procedure with reduction in following complications, such as GVHD. Identifying glycan patterns that induce self-tolerance and the ones that cause the auto- and allo-immune response could lead to innovative and tissue-specific immunomodulative therapy instead of the current immunosuppressive treatment, enabling preservation of the graft-versus-tumor effect. Moreover, improved glycan pattern analyses could offer a more complete assessment and greatly needed dynamic biomarkers for GVHD. This review is written with a goal to encourage glycan research in the field of alloHSCT and GVHD as a perspective tool leading to improved engraftment, discovery of much needed biomarkers for GVHD, enabling an appropriate therapy and improved monitoring of therapeutic response. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc. •Glycans are involved in almost every biological process.•Glycans are associated with immunological disturbances and autoimmune diseases.•GVHD is alloimmune and autoimmune disorder following alloHSCT.•Glycans have a great research potential in clarifying events after alloHSCT and GVHD.•Glycan research could lead to improved therapy and discovery of biomarkers. |
| Author | Prenc, Ema Nemet, Damir Pavletic, Steven Z. Vrhovac, Radovan Pulanic, Drazen Desnica, Lana Pezer, Marija Pucic-Bakovic, Maja |
| AuthorAffiliation | f Graft-versus-Host and Autoimmunity Section, Experimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA c University of Zagreb School of Medicine, Zagreb, Croatia d Faculty of Medicine Osijek, J. J. Strossmayer University of Osijek, Osijek, Croatia e Genos Glycoscience Research Laboratory, Zagreb, Croatia b Division of Haematology, Department of Internal Medicine, University Hospital Centre Zagreb, Zagreb, Croatia a Croatian Cooperative Group for Hematologic Diseases, Zagreb, Croatia |
| AuthorAffiliation_xml | – name: a Croatian Cooperative Group for Hematologic Diseases, Zagreb, Croatia – name: b Division of Haematology, Department of Internal Medicine, University Hospital Centre Zagreb, Zagreb, Croatia – name: f Graft-versus-Host and Autoimmunity Section, Experimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA – name: d Faculty of Medicine Osijek, J. J. Strossmayer University of Osijek, Osijek, Croatia – name: c University of Zagreb School of Medicine, Zagreb, Croatia – name: e Genos Glycoscience Research Laboratory, Zagreb, Croatia |
| Author_xml | – sequence: 1 givenname: Ema surname: Prenc fullname: Prenc, Ema organization: Croatian Cooperative Group for Hematologic Diseases, Zagreb, Croatia – sequence: 2 givenname: Drazen surname: Pulanic fullname: Pulanic, Drazen email: dpulanic@yahoo.com organization: Division of Haematology, Department of Internal Medicine, University Hospital Centre Zagreb, Zagreb, Croatia – sequence: 3 givenname: Maja surname: Pucic-Bakovic fullname: Pucic-Bakovic, Maja organization: Genos Glycoscience Research Laboratory, Zagreb, Croatia – sequence: 4 givenname: Marija surname: Pezer fullname: Pezer, Marija organization: Genos Glycoscience Research Laboratory, Zagreb, Croatia – sequence: 5 givenname: Lana surname: Desnica fullname: Desnica, Lana organization: Division of Haematology, Department of Internal Medicine, University Hospital Centre Zagreb, Zagreb, Croatia – sequence: 6 givenname: Radovan surname: Vrhovac fullname: Vrhovac, Radovan organization: Division of Haematology, Department of Internal Medicine, University Hospital Centre Zagreb, Zagreb, Croatia – sequence: 7 givenname: Damir surname: Nemet fullname: Nemet, Damir organization: Division of Haematology, Department of Internal Medicine, University Hospital Centre Zagreb, Zagreb, Croatia – sequence: 8 givenname: Steven Z. surname: Pavletic fullname: Pavletic, Steven Z. organization: Graft-versus-Host and Autoimmunity Section, Experimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26923767$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1016_j_bbagen_2016_05_001 crossref_primary_10_1016_j_jtct_2022_05_038 crossref_primary_10_3389_fimmu_2020_602547 crossref_primary_10_3389_fimmu_2021_633214 crossref_primary_10_1002_INMD_20230005 crossref_primary_10_1002_jcp_28825 |
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| Keywords | Graft versus host disease Glycosylation Glycan Hematopoietic stem cell transplantation |
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| SubjectTerms | Acute Disease Allografts Animals biomarkers Biomarkers - metabolism Biomedical Research cell transplantation Chronic Disease field experimentation Glycan Glycosylation Graft versus host disease Graft vs Host Disease - genetics Graft vs Host Disease - metabolism Graft vs Host Disease - therapy Hematopoietic Stem Cell Transplantation human diseases Humans immune system immunosuppression Immunosuppression Therapy - methods medicine monitoring oligosaccharides polysaccharides stem cells |
| Title | Potential of glycosylation research in graft versus host disease after allogeneic hematopoietic stem cell transplantation |
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