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Updated: Aug 5, 2026

High Throughput Sequential ELISA for Validation of Biomarkers of Acute Graft-Versus-Host Disease
Published on: October 31, 2012
Plasma proteins associated with chronic graft-versus-host disease organ involvement
Stephanie J Lee1, Corey Cutler2, Ningxin Ma1
1Fred Hutchinson Cancer Center, Seattle, United States of America.
Insights
Plasma protein biomarkers correlate with organ involvement in chronic graft-versus-host disease (cGVHD). However, these findings are not yet actionable for guiding treatment decisions in cGVHD patients.
Area of Science:
- Hematology
- Immunology
- Oncology
Background:
- Prior research identified plasma proteins linked to chronic graft-versus-host disease (cGVHD).
- Understanding specific organ manifestations in cGVHD is crucial for effective treatment strategies.
Purpose of the Study:
- To investigate the association between plasma protein levels and specific organ involvement in patients with cGVHD.
- To determine if plasma biomarkers can guide treatment choices for cGVHD organ manifestations.
Main Methods:
- Plasma proteins were quantified in 695 patients with cGVHD.
- Correlations between protein levels and organ involvement were analyzed using statistical adjustments.
Main Results:
- Fourteen plasma proteins showed associations with organ involvement (AUCs 0.7-0.8).
- Skin, mouth, joint, GI, lung, and liver involvement were linked to specific biomarkers.
- No combination of proteins improved predictive model fit beyond clinical variables.
Conclusions:
- Identified correlations between plasma proteins and cGVHD organ involvement.
- Current findings are not directly actionable for clinical treatment guidance.
- Future research will explore proximal determinants of cGVHD in blood and tissue.
Background:
Prior studies identified plasma proteins associated with chronic graft-versus-host disease (cGVHD). The goal of this cross-sectional study was to evaluate whether plasma biomarkers were associated with specific organ manifestations to help guide treatment choice.
Methods:
Plasma proteins were measured in patients with cGVHD (n = 695) from Chronic GVHD Consortium studies. Correlations of plasma protein levels with individual organ involvement were tested with p≤0.05 considered significant after Benjamini-Hochberg adjustment and adjustment for five baseline clinical variables.
Results:
Median time from cGVHD diagnosis to blood draw was 0.9 months (IQR 0.1-9.5). Donors were 50% HLA-matched unrelated, 32% matched related and the remainder were umbilical cord blood, haploidentical or mismatched unrelated donors. Methotrexate and calcineurin inhibitor acute GVHD (aGVHD) prophylaxis was used in 53% of patients. Overall, 326 (47%) had moderate and 244 (35%) had severe cGVHD with the following organ involvement at time of blood draw: skin (67%), mouth (60%), eye (49%), joint (34%), GI (31%), lung (23%), and liver (17%). After adjustment for batch effects and patient and transplant characteristics, fourteen plasma proteins were associated with organ involvement with independent AUCs of 0.7-0.8. All organs except eye were associated with at least one biomarker. However, no combination of plasma proteins improved model fit after adjusting for patient and transplant clinical variables.
Conclusion:
Correlations between plasma proteins and organ involvement were identified but are not actionable. Our future investigations will focus on more granular and immediately proximal determinants of cGVHD biology in both blood and tissue.
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