Increased incidence of EBV-associated lymphoproliferative disorders after allogeneic stem cell transplantation from matched unrelated donors due to a change of T cell depletion technique
- 1 February 2002
- journal article
- Published by Springer Nature in Bone Marrow Transplantation
- Vol. 29 (4), 335-339
- https://doi.org/10.1038/sj.bmt.1703362
Abstract
Here, the influence of T vs T and B cell depletion on the incidence of EBV-associated lymphoproliferative disorder (EBV-LPD) after bone marrow transplantation (BMT) from a matched unrelated donor (MUD) is analyzed. From 1982 to 1997 the soy bean agglutinin/sheep red blood cell (SBA/SRBC) method was used for T cell depletion. This technique is well established, but the use of SRBC has a risk of transmitting prions or viruses. Therefore, a new T cell depletion method was introduced, using CD2 and CD3 monoclonal antibodies (CD2/3 method) instead of SRBC. Unfortunately, this led to an unexpected high number of EBV-LPDs in patients receiving transplants from MUDs. SBA depletion was reintroduced and combined with the CD2/3 method (SBA/CD2/3) in this patient population, later replaced by B cell-specific (CD19 and CD22) antibodies (CD3/19/22 method). The number of T (x 10(5)/kg) and B (x 10(5)/kg) cells in the graft was 1.5 +/- 0.8 and 2 +/- 1 (T/B ratio 0.75), 2.2 +/- 2.0 and 41 +/- 21 (ratio 0.055), 5.0 +/- 0.0 and 2 +/- 1 (ratio 2.5), 2.5 +/- 1.2 and 10 +/- 6 (ratio 0.25) using the SBA/SRBC, CD2/3, SBA/CD2/3 and CD3/19/22 techniques, respectively. When B cell depletion was performed (SBA/SRBC, SBA/CD2/3, CD3/19/22) four out of 31 patients (13%) receiving a BMT from a MUD developed an EBV-LPD. Without B cell depletion (CD2/3) this occurred in five out of seven patients (71%) (P < 0.05). A T/B cell ratio in the graft of > or = 0.25 seems sufficient to significantly reduce the incidence of EBV-LPD after BMT from MUDs.Keywords
This publication has 14 references indexed in Scilit:
- Epstein–Barr Virus InfectionNew England Journal of Medicine, 2000
- The depletion of T cells from haematopoietic stem cell transplantsRheumatology, 1999
- Unrelated bone marrow transplantation in patients with myelodysplastic syndromes and secondary acute myeloid leukemia: an EBMT surveyBone Marrow Transplantation, 1998
- A Risk-Adapted Approach with a Short Course of Ganciclovir to Prevent Cytomegalovirus (CMV) Pneumonia in CMV-Seropositive Recipients of Allogeneic Bone Marrow TransplantsClinical Infectious Diseases, 1997
- Analysis of 462 Transplantations from Unrelated Donors Facilitated by the National Marrow Donor ProgramNew England Journal of Medicine, 1993
- Graft-versus-Host DiseaseNew England Journal of Medicine, 1991
- SEROLOGICAL AND MOLECULAR STUDIES OF EPSTEIN-BARR VIRUS INFECTION IN ALLOGENEIC MARROW GRAFT RECIPIENTSTransplantation, 1990
- Eradication of Epstein-Barr virus by allogeneic bone marrow transplantation: implications for sites of viral latency.Proceedings of the National Academy of Sciences, 1988
- TRANSPLANTATION FOR ACUTE LEUKAEMIA WITH HLA-A AND B NONIDENTICAL PARENTAL MARROW CELLS FRACTIONATED WITH SOYBEAN AGGLUTININ AND SHEEP RED BLOOD CELLSThe Lancet, 1981
- Bone-Marrow TransplantationNew England Journal of Medicine, 1975