Current status of therapeutic vaccines for non-Hodgkin's lymphoma

被引:30
作者
Hurvitz, SA [1 ]
Timmerman, JM [1 ]
机构
[1] Univ Calif Los Angeles, Los Angeles, CA USA
关键词
idiotype; immunotherapy; lymphoma; vaccines;
D O I
10.1097/01.cco.0000174040.52427.83
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review Therapeutic vaccines targeting B cell lymphoma idiotype have reached an advanced stage of clinical development, with three multicenter randomized clinical trials ongoing. This review describes the rationale and development of this immunotherapeutic approach, the design of current phase III trials, and other active vaccination approaches likely to move forward into clinical testing for lymphomas. Recent findings Several groups have achieved promising results in phase II trials of patient-specific idiotype vaccines, with very few side effects noted. Anti-idiotype vaccination. The manufacturing of autologous tumor idiotype proteins is being rapidly refined by the use of molecular technologies. Two trials involving more than 1000 patients are now under way, which use idiotype vaccination after induction chemotherapy; one trial completed accrual in early 2004. A third trial opened in 2004, using rituximab followed by idiotype vaccine with maintenance booster vaccines continuing throughout the period of normal B cell recovery. In accordance with the United States Food and Drug Administration, progression-free survival serves as the accepted primary efficacy endpoint in these studies. Summary Lymphoma idiotype vaccination represents a promising immunotherapeutic approach targeting a patient-specific tumor antigen. The results of pivotal phase III trials for three first-generation idiotype vaccines will become available in the next several years. Advanced manufacturing techniques should permit application of this tailor-made treatment to large numbers of non-Hodgkin's lymphoma patients.
引用
收藏
页码:432 / 440
页数:9
相关论文
共 82 条
[1]  
Abe A, 1996, GENE THER, V3, P988
[2]   Immunobiology of dendritic cells [J].
Banchereau, J ;
Briere, F ;
Caux, C ;
Davoust, J ;
Lebecque, S ;
Liu, YT ;
Pulendran, B ;
Palucka, K .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :767-+
[3]  
Barrios Y, 2002, HAEMATOLOGICA, V87, P400
[4]   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
[5]   Anti-idiotypic DNA vaccines for lymphoma immunotherapy require the presence of both variable region genes for tumor protection [J].
Benvenuti, F ;
Burrone, OR ;
Efremov, DG .
GENE THERAPY, 2000, 7 (07) :605-611
[6]   Characterization of cellular immune responses to a recombinant idiotype vaccine by ELISPOT and identification of MHC class I-restricted T cell epitopes by peptide mapping. [J].
Bertinetti, CM ;
Veelken, H .
BLOOD, 2004, 104 (11) :395A-395A
[7]   Genetic fusion of chemokines to a self tumor antigen induces protective, T-cell dependent antitumor immunity [J].
Biragyn, A ;
Tani, K ;
Grimm, MC ;
Weeks, S ;
Kwak, LW .
NATURE BIOTECHNOLOGY, 1999, 17 (03) :253-258
[8]   Mediators of innate immunity that target immature, but not mature, dendritic cells induce antitumor immunity when genetically fused with nonimmunogenic tumor antigens [J].
Biragyn, A ;
Surenhu, M ;
Yang, D ;
Ruffini, PA ;
Haines, BA ;
Klyushnenkova, E ;
Oppenheim, JJ ;
Kwak, LW .
JOURNAL OF IMMUNOLOGY, 2001, 167 (11) :6644-6653
[9]  
Borrello I, 2000, BLOOD, V95, P3011
[10]  
Borrello Ivan M, 2002, Cancer Control, V9, P138