Effect of combined T- and B-cell depletion of allogeneic HLA-mismatched bone marrow graft on the magnitude and kinetics of Epstein–Barr virus load in the peripheral blood of bone marrow transplant recipients
Charlotte Tammik
Department of Clinical Immunology and Center for Allogeneic Stem Cell Transplantation at Huddinge Hospital, Karolinska Institutet, Stockholm, Sweden
Search for more papers by this authorOlle Ringden
Department of Clinical Immunology and Center for Allogeneic Stem Cell Transplantation at Huddinge Hospital, Karolinska Institutet, Stockholm, Sweden
Search for more papers by this authorCharlotte Tammik
Department of Clinical Immunology and Center for Allogeneic Stem Cell Transplantation at Huddinge Hospital, Karolinska Institutet, Stockholm, Sweden
Search for more papers by this authorOlle Ringden
Department of Clinical Immunology and Center for Allogeneic Stem Cell Transplantation at Huddinge Hospital, Karolinska Institutet, Stockholm, Sweden
Search for more papers by this authorAbstract
Abstract: Recipients of T-cell-depleted bone marrow (BM) transplants (BMT) frequently develop Epstein–Barr virus (EBV)-associated post-transplant lymphoproliferative disease (PTLD) preceded by a rapid and prominent increase of EBV load in the peripheral blood. The level of this increase positively correlates with the incidence of PTLD. Using a semiquantitative PCR assay we compared the blood levels of EBV-DNA in patients transplanted with either T-cell or T- and B-cell-depleted human leukocyte antigen (HLA)-mismatched BM grafts. Combined T- and B-cell depletion correlated with significantly lower maximal levels of EBV load, which were reached with slower kinetics. These data indicate that B-cell depletion of BM can be used for prophylaxis of PTLD in BM transplant recipients and can affect the long-term balance between EBV and its host.
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