Best Practice & Research Clinical Haematology
Volume 21, Issue 2 , Pages 205-222, June 2008

Graft-versus-host disease after donor leukocyte infusions: presentation and management

  • Noelle V. Frey, MD (Instructor of Medicine)
  • ,
  • David L. Porter, MD (Professor of Medicine, Director of Allogeneic Stem Cell Transplantation Program)

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +1 215 662 2867; Fax: +1 215 662 4064.

Division of Hematology-Oncology and Abramson Cancer Center, University of Pennsylvania Medical Center, 16 Penn Tower, 3400 ISpruce St, Philadelphia PA 19106, USA

Donor leukocyte infusion (DLI) is used after both myeloablative and non-myeloablative stem-cell transplantation to treat and prevent relapse, to establish full donor chimerism, and to treat and prevent infections. The major treatment-related complication of DLI is graft-versus-host disease (GVHD). The presentation and treatment of GVHD after DLI is similar to its presentation and treatment after stem-cell transplantation, with some notable exceptions. While GVHD and graft-versus-tumor (GVT) effects are highly correlated after DLI, some patients experience remission without GVHD. Studies to define tumor-specific target antigens and GVT effector cells, as well as strategies of donor T-cell manipulation and optimization of DLI dose and schedule, may ultimately lead to the consistent ability to separate GVHD from GVT activity, improvement in the safety and specificity of DLI, and enhancement of the anti-tumor activity of donor T cells.

Key words: donor leukocyte infusion, immunotherapy, graft-versus-host disease, graft-versus-tumor effect, CD8+ depletion, T-cell inactivation, suicide gene

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1521-6926(08)00008-X

doi:10.1016/j.beha.2008.02.007

Best Practice & Research Clinical Haematology
Volume 21, Issue 2 , Pages 205-222, June 2008