4.5 Article

Potential of glycosylation research in graft versus host disease after allogeneic hematopoietic stem cell transplantation

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
Volume 1860, Issue 8, Pages 1615-1622

Publisher

ELSEVIER
DOI: 10.1016/j.bbagen.2016.02.015

Keywords

Glycan; Glycosylation; Graft versus host disease; Hematopoietic stem cell transplantation

Funding

  1. Unity Through Knowledge Fund, Croatia
  2. European Commission [278535, 305280, 324400, 315997]
  3. intramural program of the National Cancer Institute, Center for Cancer Research, National Institutes of Health, USA

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Background: 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. Scope of review: 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. Major Conclusions: Glycan research could bring significant improvement in alloHSCI. 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. General significance: 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. (C) 2016 Elsevier B.V. All rights reserved.

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