Long-term outcome of EBV-specific T-cell infusions to prevent or treat EBV-related lymphoproliferative disease in transplant recipients

被引:636
作者
Heslop, Helen E. [1 ,2 ]
Slobod, Karen S. [3 ]
Pule, Martin A. [1 ,2 ]
Hale, Gregory A. [4 ]
Rousseau, Alexandra [1 ,2 ]
Smith, Colton A. [4 ]
Bollard, Catherine M. [1 ,2 ]
Liu, Hao [5 ]
Wu, Meng-Fen [5 ]
Rochester, Richard J. [4 ]
Amrolia, Persis J. [6 ]
Hurwitz, Julia L. [4 ]
Brenner, Malcolm K. [1 ,2 ]
Rooney, Cliona M. [1 ,2 ]
机构
[1] Baylor Coll Med, Methodist Hosp, Ctr Cell & Gene Therapy, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Houston, TX 77030 USA
[3] Novartis Vaccines & Diagnost, Cambridge, MA USA
[4] St Jude Childrens Hosp, Memphis, TN 38105 USA
[5] Baylor Coll Med, Dan L Duncan Canc Ctr, Houston, TX 77030 USA
[6] Great Ormond St Childrens Hosp, Dept Bone Marrow Transplant, London, England
基金
美国国家卫生研究院;
关键词
EPSTEIN-BARR-VIRUS; ALLOGENEIC BONE-MARROW; VERSUS-HOST-DISEASE; ADOPTIVE TRANSFER; NASOPHARYNGEAL CARCINOMA; VIRAL-INFECTIONS; GENE-THERAPY; DONOR; LYMPHOCYTES; LYMPHOMA;
D O I
10.1182/blood-2009-08-239186
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
T-cell immunotherapy that takes advantage of Epstein-Barr virus (EBV) stimulated immunity has the potential to fill an important niche in targeted therapy for EBV-related cancers. To address questions of long-term efficacy, safety, and practicality, we studied 114 patients who had received infusions of EBV-specific cytotoxic T lymphocytes (CTLs) at 3 different centers to prevent or treat EBV(+) lymphoproliferative disease (LPD) arising after hematopoietic stem cell transplantation. Toxicity was minimal, consisting mainly of localized swelling at sites of responsive disease. None of the 101 patients who received CTL prophylaxis developed EBV(+) LPD, whereas 11 of 13 patients treated with CTLs for biopsy-proven or probable LPD achieved sustained complete remissions. The gene-marking component of this study enabled us to demonstrate the persistence of functional CTLs for up to 9 years. A preliminary analysis indicated that a patient-specific CTL line can be manufactured, tested, and infused for $6095, a cost that compares favorably with other modalities used in the treatment of LPD. We conclude that the CTL lines described here provide safe and effective prophylaxis or treatment for lymphoproliferative disease in transplantation recipients, and the manufacturing methodology is robust and can be transferred readily from one institution to another without loss of reproducibility. The current trial was registered at www.clinicaltrials.gov as #NCT00058812. (Blood. 2010;115:925-935)
引用
收藏
页码:925 / 935
页数:11
相关论文
共 51 条
[1]   Minor groove binder-conjugated DNA probes for quantitative DNA detection by hybridization-triggered fluorescence [J].
Afonina, IA ;
Reed, MW ;
Lusby, E ;
Shishkina, IG ;
Belousov, YS .
BIOTECHNIQUES, 2002, 32 (04) :940-+
[2]   Hematopoietic-cell transplantation at 50 [J].
Appelbaum, Frederick R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (15) :1472-1475
[3]   Adoptive transfer of effector CD8+ T cells derived from central memory cells establishes persistent T cell memory in primates [J].
Berger, Carolina ;
Jensen, Michael C. ;
Lansdorp, Peter M. ;
Gough, Mike ;
Elliott, Carole ;
Riddell, Stanley R. .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (01) :294-305
[4]   Cancer immunotherapy: A treatment for the masses [J].
Blattman, JN ;
Greenberg, PD .
SCIENCE, 2004, 305 (5681) :200-205
[5]   Molecules and mechanisms of the graft-versus-leukaemia effect [J].
Bleakley, M ;
Riddell, SR .
NATURE REVIEWS CANCER, 2004, 4 (05) :371-380
[6]   Complete responses of relapsed lymphoma following genetic modification of tumor-antigen presenting cells and T-lymphocyte transfer [J].
Bollard, Catherine M. ;
Gottschalk, Stephen ;
Leen, Ann M. ;
Weiss, Heidi ;
Straathof, Karin C. ;
Carrum, George ;
Khalil, Mariam ;
Wu, Meng-fen ;
Huls, M. Helen ;
Chang, Chung-Che ;
Gresik, M. Victoria ;
Gee, Adrian P. ;
Brenner, Malcolm K. ;
Rooney, Cliona M. ;
Heslop, Helen E. .
BLOOD, 2007, 110 (08) :2838-2845
[7]   Cytotoxic T lymphocyte therapy for Epstein-Barr virus Hodgkin's disease [J].
Bollard, CM ;
Aguilar, L ;
Straathof, KC ;
Gahn, B ;
Huls, MH ;
Rousseau, A ;
Sixbey, J ;
Gresik, MV ;
Carrum, G ;
Hudson, M ;
Dilloo, D ;
Gee, A ;
Brenner, MK ;
Rooney, CM ;
Heslop, HE .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 200 (12) :1623-1633
[8]   Outcomes of transplantation with partial T-cell depletion of matched or mismatched unrelated or partially matched related donor bone marrow in children and adolescents with leukemias [J].
Bunin, N ;
Aplenc, R ;
Leahey, A ;
Magira, E ;
Grupp, S ;
Pierson, G ;
Monos, D .
BONE MARROW TRANSPLANTATION, 2005, 35 (02) :151-158
[9]   Epstein-Barr virus (EBV) reactivation in allogeneic stem-cell transplantation:: Relationship between viral load, EBV-specific T-cell reconstitution and rituximab therapy [J].
Clave, E ;
Agbalika, F ;
Bajzik, V ;
de Latour, RP ;
Trillard, M ;
Rabian, C ;
Scieux, C ;
Devergie, A ;
Socié, G ;
Ribaud, P ;
Adès, L ;
Ferry, C ;
Gluckman, E ;
Charron, D ;
Esperou, H ;
Toubert, A ;
Moins-Teisserenc, H .
TRANSPLANTATION, 2004, 77 (01) :76-84
[10]   Adoptive transfer of cytomegalovirus-specific CTL to stem cell transplant patients after selection by HLA-peptide tetramers [J].
Cobbold, M ;
Khan, N ;
Pourgheysari, B ;
Tauro, S ;
McDonald, D ;
Osman, H ;
Assenmacher, M ;
Billingham, L ;
Steward, C ;
Crawley, C ;
Olavarria, E ;
Goldman, J ;
Chakraverty, R ;
Mahendra, P ;
Craddock, C ;
Moss, PAH .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (03) :379-386