Prompt versus preemptive intervention for EBV lymphoproliferative disease
Author:
Affiliation:
1. From the Center for Cell and Gene Therapy and the Departments of Pediatrics and Medicine, Baylor College of Medicine, Houston; the Methodist Hospital, Houston; and Texas Children's Hospital, Houston, TX.
Abstract
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/103/10/3979/1697504/zh801004003979.pdf
Reference17 articles.
1. Curtis RE, Travis LB, Rowlings PA, et al. Risk of lymphoproliferative disorders after bone marrow transplantation: a multi-institutional study. Blood. 1999;94: 2208-2216.
2. Kuehnle I, Huls MH, Liu Z, et al. CD20 monoclonal antibody (rituximab) for therapy of Epstein-Barr virus lymphoma after hemopoietic stem-cell transplantation. Blood. 2000;95: 1502-1505.
3. van Esser JW, Niesters HG, van der HB, et al. Prevention of Epstein-Barr virus–lymphoproliferative disease by molecular monitoring and preemptive rituximab in high-risk patients after allogeneic stem cell transplantation. Blood. 2002;99: 4364-4369.
4. Carpenter PA, Appelbaum FR, Corey L, et al. A humanized non-FcR–binding anti-CD3 antibody, visilizumab, for treatment of steroid-refractory acute graft-versus-host disease. Blood. 2002;99: 2712-2719.
5. Rooney CM, Smith CA, Ng CYC, et al. Infusion of cytotoxic T cells for the prevention and treatment of Epstein-Barr virus–induced lymphoma in allogeneic transplant recipients. Blood. 1998;92: 1549-1555.
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