Allogeneic cytotoxic T-cell therapy for EBV-positive posttransplantation lymphoproliferative disease: results of a phase 2 multicenter clinical trial

被引:478
作者
Haque, Tanzina [1 ]
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.
机构
[1] Univ Edinburgh, Clin & Mol Virol Lab, Edinburgh, Midlothian, Scotland
[2] Inst Canc Res, Sutton, Surrey, England
[3] Royal Infirm, Scottish Natl Blood Transfus Serv, Edinburgh, Midlothian, Scotland
[4] Royal Infirm, Dept Pathol, Edinburgh, Midlothian, Scotland
[5] UCL, Royal Free Hosp, Sch Med, Dept Immunol, London, England
[6] Birmingham Childrens Hosp, Liver Unit, Birmingham, W Midlands, England
[7] Royal Infirm Edinburgh NHS Trust, Liver Transplant Unit, Edinburgh, Midlothian, Scotland
[8] Queensland Inst Med Res, Immunohaematol Lab, Brisbane, Qld 4006, Australia
关键词
D O I
10.1182/blood-2006-12-063008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We present the results of a multicenter clinical trial using Epstein-Barr virus (EBV)-specific cytotoxic T lymphocytes (CTLs) generated from EBV-seropositive blood donors to treat patients with EBV-positive posttransplantation lymphoproliferative disease (PTLD) on the basis of the best HLA match and specific in vitro cytotoxicity. Thirty-three PTLD patients who had failed on conventional therapy were enrolled. No adverse effects of CTL infusions were observed and the response rate (complete or partial) in 33 patients was 64% at 5 weeks and 52% at 6 months. Fourteen patients achieved a complete remission, 3 showed a partial response, and 16 had no response at 6 months (5 died before completing treatment). At 5 weeks, there was a significant trend toward better responses with higher numbers of CD4+ cells in infused CTL lines (P=.001) that were maintained at 6 months (P=.001). Patients receiving CTLs with closer HLA matching responded better at 6 months (P =.048). Female patients responded better than male patients, but the differences were not statistically significant. Our results show that allogeneic CTLs are a safe and rapid therapy for PTLD, bypassing the need to grow CTLs for individual patients. The response rate in this poor prognosis patient group is encouraging.
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收藏
页码:1123 / 1131
页数:9
相关论文
共 29 条
[1]   Epstein-Barr virus-specific cytotoxic T-lymphocytes for adoptive immunotherapy of post-transplant lymphoproliferative disease [J].
Burns, DM ;
Crawford, DH .
BLOOD REVIEWS, 2004, 18 (03) :193-209
[2]   Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas [J].
Cheson, BD ;
Horning, SJ ;
Coiffier, B ;
Shipp, MA ;
Fisher, RI ;
Connors, JM ;
Lister, TA ;
Vose, J ;
Grillo-López, A ;
Hagenbeek, A ;
Cabanillas, F ;
Klippensten, D ;
Hiddemann, W ;
Castellino, R ;
Harris, NL ;
Armitage, JO ;
Carter, W ;
Hoppe, R ;
Canellos, GP .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1244-1253
[3]   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
[4]   A cohort study among University students: Identification of risk factors for Epstein-Barr virus seroconversion and infectious mononucleosis [J].
Crawford, DH ;
Macsween, KF ;
Higgins, CD ;
Thomas, R ;
McAulay, K ;
Williams, H ;
Harrison, N ;
Reid, S ;
Conacher, M ;
Douglas, J ;
Swerdlow, AJ .
CLINICAL INFECTIOUS DISEASES, 2006, 43 (03) :276-282
[5]   Biology and disease associations of Epstein-Barr virus [J].
Crawford, DH .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2001, 356 (1408) :461-473
[6]   Human CD62L- memory T cells are less responsive to alloantigen stimulation than CD62L+ naive T cells:: potential for adoptive immunotherapy and allodepletion [J].
Foster, AE ;
Marangolo, M ;
Sartor, MM ;
Alexander, SI ;
Hu, M ;
Bradstock, KF ;
Gottlieb, DJ .
BLOOD, 2004, 104 (08) :2403-2409
[7]   Epstein-Barr virus (EBV) load in bone marrow transplant recipients at risk to develop posttransplant lymphoproliferative disease:: prophylactic infusion of EBV-specific cytotoxic T cells [J].
Gustafsson, Å ;
Levitsky, V ;
Zou, JZ ;
Frisan, T ;
Dalianis, T ;
Ljungman, P ;
Ringden, O ;
Winiarski, J ;
Ernberg, I ;
Masucci, MG .
BLOOD, 2000, 95 (03) :807-814
[8]   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
[9]  
Haque T, 1998, J IMMUNOL, V160, P6204
[10]   Long-term restoration of immunity against Epstein-Barr virus infection by adoptive transfer of gene-modified virus-specific T lymphocytes [J].
Heslop, HE ;
Ng, CYC ;
Li, CF ;
Smith, CA ;
Loftin, SK ;
Krance, RA ;
Brenner, MK ;
Rooney, CM .
NATURE MEDICINE, 1996, 2 (05) :551-555