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Potential Novel Biomarkers in Chronic Graft-Versus-Host Disease

Authors :
Hildegard Greinix
Nina Milutin Gašperov
Daniel Wolff
Magdalena Grce
Maja Pučić-Baković
Nuala Mooney
Dražen Pulanić
Ernst Holler
Daniela Weber
Katarzyna Bogunia-Kubik
Rachel E Crossland
Francesca Perutelli
Marit Inngjerdingen
Anne M. Dickinson
Newcastle University [Newcastle]
Department of clinical and biological sciences, University of Torino, Italy
Polish Academy of Sciences (PAN)
Immunologie humaine, physiopathologie & immunothérapie (HIPI (UMR_S_976 / U976))
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP)
Ruđer Bosˇ kovic ́ Institute
Glycoscience Research Laboratory
Medical University of Graz
University Hospital Regensburg
University Hospital Centre Zagreb and University of Zagreb School of Medicine
University of Oslo (UiO)
Institut Ruđer Bošković (IRB)
Mooney, Nuala
Università degli studi di Torino = University of Turin (UNITO)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité)
Source :
Frontiers in Immunology, Frontiers in Immunology, Frontiers, 2020, 11, ⟨10.3389/fimmu.2020.602547⟩, Frontiers in Immunology, Vol 11 (2020)
Publication Year :
2020
Publisher :
HAL CCSD, 2020.

Abstract

Prognostic, diagnostic or predictive biomarkers are urgently needed for assessment of chronic graft-versus-host disease (cGvHD), a major risk for patients undergoing allogeneic hematopoietic stem cell transplantation. The main goal of this review generated within the COST Action EUROGRAFT “Integrated European Network on Chronic Graft Versus Host Disease” was to identify potential novel biomarkers for cGvHD besides the widely accepted molecular and cellular biomarkers. Thus, the focus was on cellular biomarkers, alloantibodies, glycomics, endothelial derived particles, extracellular vesicles, microbiome, epigenetic and neurologic changes in cGvHD patients. Both host-reactive antibodies in general, and particularly alloantibodies have been associated with cGvHD and require further consideration. Glycans attached to IgG modulate its activity and represent a promising predictive and/or stratification biomarker for cGVHD. Furthermore, epigenetic changes such as microRNAs and DNA methylation represent potential biomarkers for monitoring cGvHD patients and novel targets for developing new treatment approaches. Finally, the microbiome likely affects the pathophysiology of cGvHD; bacterial strains as well as microbial metabolites could display potential biomarkers for dysbiosis and risk for the development of cGvHD. In summary, although there are no validated biomarkers currently available for clinical use to better inform on the diagnosis, prognosis or prediction of outcome for cGvHD, many novel sources of potential markers have shown promise and warrant further investigation using well characterized, multi-center patient cohorts.

Details

Language :
English
ISSN :
16643224
Database :
OpenAIRE
Journal :
Frontiers in Immunology, Frontiers in Immunology, Frontiers, 2020, 11, ⟨10.3389/fimmu.2020.602547⟩, Frontiers in Immunology, Vol 11 (2020)
Accession number :
edsair.doi.dedup.....3c611cebbb3b17fd98d054e7dd0896c9