Successful treatment of EBV-associated posttransplantation lymphoma after cord blood transplantation using third-party EBV-specific cytotoxic T lymphocytes

被引:173
作者
Barker, Juliet N. [1 ,2 ]
Doubrovina, Ekaterina [3 ]
Sauter, Craig [1 ]
Jaroscak, Jennifer J.
Perales, Miguel A. [1 ,2 ]
Doubrovin, Mikhail [4 ]
Prockop, Susan E. [3 ]
Koehne, Guenther [1 ,2 ]
O'Reilly, Richard J. [1 ,2 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Allogene Bone Marrow Transplant Serv, New York, NY 10065 USA
[2] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Pediat, Allogene Bone Marrow Transplant Serv, New York, NY 10065 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Nucl Med, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
LYMPHOPROLIFERATIVE DISEASE; CELLS; DISORDERS; RITUXIMAB; SELECTION; THERAPY; PHASE-2;
D O I
10.1182/blood-2010-04-281873
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cellular therapy of Epstein-Barr virus (EBV)(+) posttransplantation lymphoproliferative diseases (PTLD) in cord blood transplant (CBT) recipients is limited by lack of donor access and the donor's naive neonatal immune system. We therefore used partially human leukocyte antigen-matched third-party in vitro expanded EBV-specific cytotoxic T lymphocytes (CTLs) to treat 2 CBT recipients with life-threatening, donor-derived monoclonal EBV(+) diffuse large B-cell lymphomas with extranodal involvement developing in the context of graft-versus-host disease. Both patients had failed immunosuppression taper and Rituximab. After 5 and 9 infusions of 106 EBV-CTL/kg, respectively, each patient achieved a sustained complete remission without toxicity or graft-versus-host disease. Each is alive without recurrence at 20 and 15 months, respectively, post-EBV-PTLD diagnosis. This approach demonstrates the efficacy of using "off-the-shelf," virus-specific third-party CTLs restricted by human leukocyte antigens expressed by the tumor to treat otherwise lethal EBV-PTLD. Such therapy may also be applicable to the treatment of other infections and residual or recurrent malignancy after CBT. (Blood. 2010;116(23):5045-5049)
引用
收藏
页码:5045 / 5049
页数:5
相关论文
共 15 条
[1]   Low incidence of Epstein-Barr virus-associated posttransplantation lymphoproliferative disorders in 272 unrelated-donor umbilical cord blood transplant recipients [J].
Barker, JN ;
Martin, PL ;
Coad, JE ;
DeFor, T ;
Trigg, ME ;
Kurtzberg, J ;
Weisdorf, DJ ;
Wagner, JE .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2001, 7 (07) :395-399
[2]   Monitoring and Preemptive Rituximab Therapy for Epstein-Barr Virus Reactivation after Antithymocyte Globulin Containing Nonmyeloablative Conditioning for Umbilical Cord Blood Transplantation [J].
Blaes, Anne H. ;
Cao, Qing ;
Wagner, John E. ;
Young, Jo-Anne H. ;
Weisdorf, Daniel J. ;
Brunstein, Claudio G. .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2010, 16 (02) :287-291
[3]   Marked increased risk of Epstein-Barr virus-related complications with the addition of antithymocyte globulin to a nonmyeloablative conditioning prior to unrelated umbilical cord blood transplantation [J].
Brunstein, Claudio G. ;
Weisclorf, Daniel J. ;
DeFor, Todd ;
Barker, Juliet N. ;
Tolar, Jakub ;
van Burik, Jo-Anne H. ;
Wagner, John E. .
BLOOD, 2006, 108 (08) :2874-2880
[4]   Efficacy and safety of rituximab in B-cell post-transplantation lymphoproliferative disorders:: results of a prospective multicenter phase 2 study [J].
Choquet, S ;
Leblond, V ;
Herbrecht, R ;
Socié, G ;
Stoppa, AM ;
Vandenberghe, P ;
Fischer, A ;
Morschhauser, F ;
Salles, G ;
Feremans, W ;
Vilmer, E ;
Peraldi, MN ;
Lang, P ;
Lebranchu, Y ;
Oksenhendler, E ;
Garnier, JL ;
Lamy, T ;
Jaccard, A ;
Ferrant, A ;
Offner, F ;
Hermine, O ;
Moreau, A ;
Fafi-Kremer, S ;
Morand, P ;
Chatenoud, L ;
Berriot-Varoqueaux, N ;
Bergougnoux, L ;
Milpied, N .
BLOOD, 2006, 107 (08) :3053-3057
[5]   Functionally active virus-specific T cells that target CMV, adenovirus, and EBV can be expanded from naive T-cell populations in cord blood and will target a range of viral epitopes [J].
Hanley, Patrick J. ;
Cruz, Conrad Russell Young ;
Savoldo, Barbara ;
Leen, Ann M. ;
Stanojevic, Maja ;
Khalil, Mariam ;
Decker, William ;
Molldrem, Jeffrey J. ;
Liu, Hao ;
Gee, Adrian P. ;
Rooney, Cliona M. ;
Heslop, Helen E. ;
Dotti, Gianpietro ;
Brenner, Malcolm K. ;
Shpall, Elizabeth J. ;
Bollard, Catherine M. .
BLOOD, 2009, 114 (09) :1958-1967
[6]   Treatment of Epstein-Barr-virus-positive post-transplantation lymphoproliferative disease with partly HLA-matched allogeneic cytotoxic T cells [J].
Haque, T ;
Wilkie, GM ;
Taylor, C ;
Amlot, PL ;
Murad, P ;
Iley, A ;
Dombagoda, D ;
Britton, KM ;
Swerdlow, AJ ;
Crawford, DH .
LANCET, 2002, 360 (9331) :436-442
[7]   Allogeneic cytotoxic T-cell therapy for EBV-positive posttransplantation lymphoproliferative disease: results of a phase 2 multicenter clinical trial [J].
Haque, Tanzina ;
Wilkie, Gwen M. ;
Jones, Marie M. ;
Higgins, Craig D. ;
Urquhart, Gillian ;
Wingate, Phoebe ;
Burns, David ;
McAulay, Karen ;
Turner, Marc ;
Bellamy, Christopher ;
Amlot, Peter L. ;
Kelly, Deirdre ;
MacGilchrist, Alastair ;
Gandhi, Maher K. ;
Swerdlow, Anthony J. ;
Crawford, Dorothy H. .
BLOOD, 2007, 110 (04) :1123-1131
[8]   Long-term outcome of EBV-specific T-cell infusions to prevent or treat EBV-related lymphoproliferative disease in transplant recipients [J].
Heslop, Helen E. ;
Slobod, Karen S. ;
Pule, Martin A. ;
Hale, Gregory A. ;
Rousseau, Alexandra ;
Smith, Colton A. ;
Bollard, Catherine M. ;
Liu, Hao ;
Wu, Meng-Fen ;
Rochester, Richard J. ;
Amrolia, Persis J. ;
Hurwitz, Julia L. ;
Brenner, Malcolm K. ;
Rooney, Cliona M. .
BLOOD, 2010, 115 (05) :925-935
[9]   How I treat EBV lymphoproliferation [J].
Heslop, Helen E. .
BLOOD, 2009, 114 (19) :4002-4008
[10]   Quantitation, selection, and functional characterization of Epstein-Barr virus-specific and alloreactive T cells detected by intracellular interferon-γ production and growth of cytotoxic precursors [J].
Koehne, G ;
Smith, KM ;
Ferguson, TL ;
Williams, RY ;
Heller, G ;
Pamer, EG ;
Dupont, B ;
O'Reilly, RJ .
BLOOD, 2002, 99 (05) :1730-1740