Simultaneous development of lymphoma in recipients of renal transplants from a single donor: donor origin confirmed by human leukocyte antigen staining and microsatellite analysis

TitleSimultaneous development of lymphoma in recipients of renal transplants from a single donor: donor origin confirmed by human leukocyte antigen staining and microsatellite analysis
Publication TypeJournal Article
Year of Publication2005
AuthorsCaillard S, Pencreach E, Braun L, Marcellin L, Jaegle ML, Wolf P, Parissiadis A, Hannedouche T, Gaub MP, Moulin B
JournalTransplantation
Volume79
Issue1
Pagination79 - 84
Date PublishedJan 15
ISSN0041-1337 (Print) 0041-1337 (Linking)
Accession Number15714173
Keywords*Microsatellite Repeats, *Tissue Donors, Adult, Female, Gene Rearrangement, Genes, Immunoglobulin, HLA Antigens / *analysis, Humans, Immunohistochemistry, Kidney Transplantation / *adverse effects, Lymphoma / *etiology, Male, Middle Aged
Abstract

BACKGROUND: Posttransplant lymphoproliferative disorders (PTLD) occur in 0.5% to 2.5% of cases in renal-transplant recipients. Epstein-Barr virus (EBV) is usually detected in the tumor cells, suggesting a role for this virus as an agent of B-cell proliferation. It is unusual for patients receiving allografts from the same donor to develop PTLD simultaneously. METHODS: we describe two patients who received renal allografts from the same donor and developed PTLD simultaneously. The presence of EBV in both tumors was confirmed. In this report, the origin of tumor cells was determined by immunohistochemical human leukocyte antigen (HLA) typing and microsatellite analysis. Clonality was studied by immunoglobulin gene rearrangement analysis. RESULTS: Our results suggest that the tumor originated from donor cells in both patients but, because immunoglobulin gene rearrangements were different, this could mean that lymphoid cells proliferate independently in each recipient. CONCLUSIONS: We propose the following pathogenesis: immortalization of passenger B lymphocytes by EBV, proliferation of these cells, and development of PTLD by means of immunosuppression, antigenic stimulation, and HLA mismatch.

DOI
Notify Library Reference ID278

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