Potential Novel Biomarkers in Chronic Graft-Versus-Host Disease

Rachel E Crossland1, Francesca Perutelli2, Katarzyna Bogunia-Kubik3

  • 1Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.

Frontiers in Immunology
|January 11, 2021
PubMed

Insights

Novel biomarkers for chronic graft-versus-host disease (cGvHD) are crucial. This review highlights promising areas like alloantibodies, glycomics, epigenetics, and the microbiome for improved cGvHD assessment.

Area of Science:

  • Hematology
  • Immunology
  • Biomarker Discovery

Background:

  • Chronic graft-versus-host disease (cGvHD) is a significant risk following allogeneic hematopoietic stem cell transplantation.
  • There is an urgent need for reliable prognostic, diagnostic, and predictive biomarkers for cGvHD.
  • Current assessment relies on widely accepted molecular and cellular markers, necessitating exploration of novel avenues.

Purpose of the Study:

  • To identify potential novel biomarkers for cGvHD beyond established markers.
  • To review emerging areas including cellular biomarkers, alloantibodies, glycomics, endothelial particles, extracellular vesicles, microbiome, and epigenetic/neurologic changes.
  • To assess their potential for diagnosis, prognosis, and prediction of outcomes in cGvHD.

Main Methods:

  • Systematic review of literature on cGvHD biomarkers.
  • Focus on non-traditional sources such as alloantibodies, glycomic profiles, microbiome alterations, and epigenetic modifications.
  • Analysis of host-reactive antibodies, IgG glycans, microRNAs, DNA methylation, bacterial strains, and microbial metabolites.

Main Results:

  • Alloantibodies and specific IgG glycan patterns show promise as predictive/stratification biomarkers for cGvHD.
  • Epigenetic changes (microRNAs, DNA methylation) may serve as monitoring biomarkers and therapeutic targets.
  • Microbiome alterations and metabolites are implicated in cGvHD pathophysiology and could indicate dysbiosis and risk.

Conclusions:

  • While no validated biomarkers are currently available for clinical cGvHD assessment, several novel sources show significant promise.
  • Further investigation in well-characterized, multi-center patient cohorts is warranted.
  • These emerging biomarkers could improve the diagnosis, prognosis, and prediction of outcomes for cGvHD patients.