EBV Related B Cell Lymphoproliferative Disease after T Depleted Mismatched Bone Marrow Transplantation

  • R. S. Shapiro
  • K. McClain
  • B. Blazar
  • J. Greenberg
  • D. Patton
  • K. Gajl-Peczalska
  • B. Burke
  • G. Frizzera
  • J. Kersey
  • A. H. Filipovich
Part of the Experimental Biology and Medicine book series (EBAM, volume 15)

Abstract

Bone marrow transplantation (BMT) can be life saving for patients with otherwise fatal malignant and non-malignant diseases. Since the majority of people lack an HLA identical sibling much effort has gone into the use of partially mismatched donors. The major obstacles in mismatched BMT have been graft rejection and severe graft vs. host disease. At the University of Minnesota we have experienced an additional complication of mismatched BMT; B cell lymphproliferative disease (BLPD) associated with EBV. Five of twenty one (24$) recipients of T depleted mismatched BMT developed fatal overwhelming lymphoproliferative processes in comparison to the very low incidence in matched T depleted (0/25) or matched non-depleted (1/>500) setting. It is clear that this subgroup of BMT recipients is at an alarmingly increased risk of developing this complication.

Keywords

Bone Marrow Transplantation Graft Rejection Burkitts Lymphoma Host Disease Solid Organ Transplant Recipient 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. 1.
    D. W. Hanto, G. Frizzera, K. J. Gajl-Peczalska, R. L. Simmons, Transplantation. 39, 461 (1985).PubMedCrossRefGoogle Scholar
  2. 2.
    D. W. Hanto, G. Frizzera, K. J. Gajl-Peczalska, NEJM, 306, 913 (1982).PubMedCrossRefGoogle Scholar
  3. 3.
    G. Frizzera, D. W. Hanto, K. J. Gajl-Peczalska, J. Rosai, R. W. McKenna, R.K. Sibley, K. P. Holahan, L. L. Lindquist, Cancer Research, 41, 4262 (1981).PubMedGoogle Scholar
  4. 4.
    D. Wang, D. Liebowitz, E. Krieff, Cell, 43, 831 (1985).PubMedCrossRefGoogle Scholar
  5. 5.
    T. Gossett, R. Gale, H. Fleischman, G. E. Austin, R. S. Sparkes, C. R. Taylor, NEJM, 300, 904 (1979).PubMedCrossRefGoogle Scholar
  6. 6.
    W. Schubach, G. Miller, E. D. Thomas, Blood, 65, 535 (1985).PubMedGoogle Scholar
  7. 7.
    W. T. Shearer, J. Ritz, M. J. Finegold, C. Guerra, H. M. Rosenblatt, et al, NEJM 312, 1151 (1985).PubMedCrossRefGoogle Scholar
  8. 8.
    N. Kapoor, L. K. L. Jung, D. Engelhard, J. Filler, I. Shalit, K. S. Landreth, R. A. Good, J Peds, 108, 435 (1986).CrossRefGoogle Scholar

Copyright information

© The Humana Press Inc. 1987

Authors and Affiliations

  • R. S. Shapiro
    • 1
  • K. McClain
    • 1
  • B. Blazar
    • 1
  • J. Greenberg
    • 1
  • D. Patton
    • 1
  • K. Gajl-Peczalska
    • 1
  • B. Burke
    • 1
  • G. Frizzera
    • 1
  • J. Kersey
    • 1
  • A. H. Filipovich
    • 1
  1. 1.University of MinnesotaMinneapolisUSA

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