Lymphoma immunotherapy: vaccines, adoptive cell transfer and immunotransplant

被引:7
作者
Brody, J. [1 ]
Levy, R. [1 ]
机构
[1] Stanford Univ, Med Ctr, Dept Med, Div Oncol, Stanford, CA 94305 USA
关键词
adoptive transfer; chimeric antigen receptor; clinical trial; dendritic cell; idiotype immunotherapy; immunotransplant; lymphoma; vaccine; COLONY-STIMULATING FACTOR; CYTOTOXIC T-LYMPHOCYTES; BONE-MARROW-TRANSPLANTATION; ACTIVATED KILLER-CELLS; NON-HODGKINS-LYMPHOMA; PHASE-I TRIAL; IMMUNE-RESPONSES; IDIOTYPE VACCINATION; MEDIATED CYTOTOXICITY; MOLECULAR REMISSIONS;
D O I
10.2217/IMT.09.50
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Therapy for non-Hodgkin lymphoma has benefited greatly from basic science and clinical research such that chemotherapy and monoclonal antibody therapy have changed some lymphoma subtypes from uniformly lethal to curable, but the majority of lymphoma patients remain incurable. Novel therapies with less toxicity and more specific targeting of tumor cells are needed and immunotherapy is among the most promising of these. Recently completed randomized trials of idiotype vaccines and earlier-phase trials of other vaccine types have shown the ability to induce antitumor T cells and some clinical responses. More recently, trials of adoptive transfer of antitumor T cells have demonstrated techniques to increase the persistence and antitumor effect of these cells. Herein, we discuss lymphoma immunotherapy clinical trial results and what lessons can be taken to improve their effect, including the combination of vaccination and adoptive transfer in an approach we have dubbed 'immunotransplant'.
引用
收藏
页码:809 / 824
页数:16
相关论文
共 109 条
[1]  
ABRAMS SI, 1988, J IMMUNOL, V140, P2090
[2]  
ALBERTINI MR, 1990, CANCER-AM CANCER SOC, V66, P2457, DOI 10.1002/1097-0142(19901215)66:12<2457::AID-CNCR2820661203>3.0.CO
[3]  
2-L
[4]  
[Anonymous], SURVEILLANCE EPIDEMI
[5]   Protective antibody responses to pneumococcal conjugate vaccine after autologous hematopoietic stem cell transplantation [J].
Antin, JH ;
Guinan, EC ;
Avigan, D ;
Soiffer, RJ ;
Joyce, RM ;
Martin, VJ ;
Molrine, DC .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2005, 11 (03) :213-222
[6]   Tumor regression in cancer patients by very low doses of a T cell-engaging antibody [J].
Bargou, Ralf ;
Leo, Eugen ;
Zugmaier, Gerhard ;
Klinger, Matthias ;
Goebeler, Mariele ;
Knop, Stefan ;
Noppeney, Richard ;
Viardot, Andreas ;
Hess, Georg ;
Schuler, Martin ;
Einsele, Hermann ;
Brandl, Christian ;
Wolf, Andreas ;
Kirchinger, Petra ;
Klappers, Petra ;
Schmidt, Margit ;
Riethmueller, Gert ;
Reinhardt, Carsten ;
Baeuerle, Patrick A. ;
Kufer, Peter .
SCIENCE, 2008, 321 (5891) :974-977
[7]  
Barrios Y, 2002, HAEMATOLOGICA, V87, P400
[8]   Complete molecular remissions induced by patient-specific vaccination plus granulocyte-monocyte colony-stimulating factor against lymphoma [J].
Bendandi, M ;
Gocke, CD ;
Kobrin, CB ;
Benko, FA ;
Sternas, LA ;
Pennington, R ;
Watson, TM ;
Reynolds, CW ;
Gause, BL ;
Duffey, PL ;
Jaffe, ES ;
Creekmore, SP ;
Longo, DL ;
Kwak, LW .
NATURE MEDICINE, 1999, 5 (10) :1171-1177
[9]  
BENYUNES MC, 1995, BONE MARROW TRANSPL, V16, P283
[10]   Systemic interleukin-2 and adoptive transfer of lymphokine-activated killer cells improves antibody-dependent cellular cytotoxicity in patients with relapsed B-cell lymphoma treated with rituximab [J].
Berdeja, Jesus G. ;
Hess, Allan ;
Lucas, David M. ;
O'Donnell, Paul ;
Ambinder, Richard F. ;
Diehl, Louis F. ;
Carter-Brookins, Denise ;
Newton, Susan ;
Flinn, Ian W. .
CLINICAL CANCER RESEARCH, 2007, 13 (08) :2392-2399