Best Practice & Research Clinical Haematology
Volume 21, Issue 2 , Pages 101-117, June 2008

GVHD pathophysiology: is acute different from chronic?

  • Tomomi Toubai (Postdoctoral Fellow, Department of Internal Medicine)
  • ,
  • Yaping Sun (Postdoctoral Fellow, Department of Internal Medicine)
  • ,
  • Pavan Reddy (Assistant Professor of Medicine)

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +1 734 647 5954; Fax: +1 734 647 9271.

Blood and Marrow Transplantation Program, Department of Internal Medicine, Division of Hematology/Oncology, University of Michigan Comprehensive Cancer Center, 1500 East Medical Center Drive, Ann Arbor, MI 48109-0942, USA

Graft-versus-host disease (GVHD) is the major complication of allogeneic hematopoietic cell transplantation (HCT). GVHD occurs in acute and chronic forms. Acute GVHD usually manifests within 100 days following HSCT. It is induced by donor T cells responding to the mismatched host polymorphic histocompatibility antigens. Chronic GVHD generally manifests later (>100 days) and has some features of autoimmune diseases. It may develop either de novo or following resolution of – or as an extension of – acute GVHD. Chronic GVHD is also thought to be induced by donor T cells, but the nature of relevant antigens, the critical cellular subsets and the mechanisms of chronic GVHD remain less well understood. In this chapter we briefly discuss and contrast the pathophysiologies of acute and chronic GVHD.

Key words: allogeneic hematopoietic stem cell transplantation, antigen-presenting cells (APC), T cells, cytokines, minor histocompatibility (miHAs)

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PII: S1521-6926(08)00006-6

doi:10.1016/j.beha.2008.02.005

Best Practice & Research Clinical Haematology
Volume 21, Issue 2 , Pages 101-117, June 2008