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Updated: Jun 27, 2026

Bone Marrow Transplantation Platform to Investigate the Role of Dendritic Cells in Graft-versus-Host Disease
Published on: March 17, 2020
Recognizing and managing chronic graft-versus-host disease
Stephanie J Lee1, Mary E D Flowers
1Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. sjlee@fhcrc.org
Insights
Chronic graft-versus-host disease (GVHD), an immune complication of hematopoietic cell transplantation (HCT), often affects skin and mouth. Prompt diagnosis and corticosteroid-based therapy are crucial for managing this condition.
Area of Science:
- Immunology
- Hematology
- Transplantation Medicine
Background:
- Chronic graft-versus-host disease (GVHD) is a frequent immune-mediated complication following allogeneic hematopoietic cell transplantation (HCT).
- While typically diagnosed within the first year post-HCT, a subset of cases (5-10%) presents beyond the first year.
- Commonly affects skin and mouth, but can involve virtually any organ system, necessitating accurate diagnosis for timely intervention.
Purpose of the Study:
- To review common clinical presentations of chronic GVHD.
- To outline principles for managing chronic GVHD.
- To summarize secondary treatment options and ongoing clinical trials, incorporating new concepts from the 2004 NIH consensus conference.
Main Methods:
- Review of literature focusing on chronic GVHD diagnosis, management, and consensus criteria.
- Discussion of clinical presentations, initial and secondary treatment strategies.
- Summary of frequently used secondary therapies and ongoing clinical trials.
Main Results:
- Consensus criteria for chronic GVHD diagnosis, scoring, pathology, biomarkers, and response criteria were developed following a 2004 NIH conference.
- Corticosteroid-based therapy is the recommended initial treatment for chronic GVHD.
- Optimal secondary treatment remains undefined, with various agents showing potential benefits.
Conclusions:
- Accurate and prompt diagnosis of chronic GVHD is critical to initiate appropriate therapy, minimizing symptoms and preventing irreversible organ damage.
- While initial treatment involves corticosteroids, secondary treatment options are diverse and require further investigation.
- New concepts from the NIH consensus conference provide a framework for understanding and managing chronic GVHD, guiding future research and clinical practice.
Abstract:
Chronic graft-versus-host disease (GVHD) is an immune-mediated disorder that occurs frequently after allogeneic hematopoietic cell transplantation (HCT). Most cases are diagnosed within the first year at a median of 4 to 6 months after HCT, but 5-10% of cases are initially diagnosed beyond the first post-transplant year. Chronic GVHD most often involves the skin and mouth, but almost any other organ system can be involved. Correct diagnosis is critical so that appropriate therapy can be started promptly to minimize symptoms and prevent irreversible organ damage. Initial treatment should be with cortico-steroid-based therapy. Optimal secondary treatment as not been established, although a large number of agents may provide benefits. A 2004 NIH conference focused on development of consensus criteria for chronic GVHD. Six papers published in 2005 and 2006 propose consensus definitions for chronic GVHD diagnosis and scoring, pathology, biomarkers, response criteria, supportive care and design of clinical trials. This review will focus on common clinical presentations and principles for managing chronic GVHD. The most frequently used secondary therapies and ongoing trials are summarized. New concepts from the NIH consensus conference are discussed.
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