Regenerating islet-derived 3-alpha is a biomarker of gastrointestinal graft-versus-host disease.

Publication Type:

Journal Article

Source:

Blood, Volume 118, Issue 25, p.6702-8 (2011)

Keywords:

2011, Adolescent, Adult, Aged, Amino Acid Sequence, Antigens, Neoplasm, Biological Markers, Center-Authored Paper, Child, Child, Preschool, Gastrointestinal Tract, Graft vs Host Disease, hematopoietic stem cell transplantation, Humans, Infant, Infant, Newborn, Lectins, C-Type, Middle Aged, Molecular Sequence Data, Multivariate Analysis, Predictive Value of Tests, Prognosis, PROTEOMICS, Public Health Sciences Division, Risk Factors, Survival Analysis, Time Factors, Tumor Markers, Biological, Young Adult

Abstract:

There are no plasma biomarkers specific for GVHD of the gastrointestinal (GI) tract, the GVHD target organ most associated with nonrelapse mortality (NRM) following hematopoietic cell transplantation (HCT). Using an unbiased, large-scale, quantitative proteomic discovery approach to identify candidate biomarkers that were increased in plasma from HCT patients with GI GVHD, 74 proteins were increased at least 2-fold; 5 were of GI origin. We validated the lead candidate, REG3α, by ELISA in samples from 1014 HCT patients from 3 transplantation centers. Plasma REG3α concentrations were 3-fold higher in patients at GI GVHD onset than in all other patients and correlated most closely with lower GI GVHD. REG3α concentrations at GVHD onset predicted response to therapy at 4 weeks, 1-year NRM, and 1-year survival (P ≤ .001). In a multivariate analysis, advanced clinical stage, severe histologic damage, and high REG3α concentrations at GVHD diagnosis independently predicted 1-year NRM, which progressively increased with higher numbers of onset risk factors present: 25% for patients with 0 risk factors to 86% with 3 risk factors present (P < .001). REG3α is a plasma biomarker of GI GVHD that can be combined with clinical stage and histologic grade to improve risk stratification of patients.