Transimmunization, a novel approach for tumor immunotherapy

被引:49
作者
Berger, CL [1 ]
Hanlon, D [1 ]
Kanada, D [1 ]
Girardi, M [1 ]
Edelson, RL [1 ]
机构
[1] Yale Univ, Sch Med, Dept Dermatol, New Haven, CT 06510 USA
关键词
D O I
10.1016/S1473-0502(02)00014-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This review describes our experience with the development of a novel form of immunotherapy that may represent the first practical and effective means of performing tumor-loaded dendritic cell (DC) immunotherapy. We have modified the highly successful extracorporeal photopheresis (ECP) treatment that has been used in the therapy of cutaneous T cell lymphoma (CTCL), autoimmune disease, transplantation rejection episodes and graft-versus-host disease to enhance its efficacy by the addition of an overnight incubation period. This adaption of ECP is termed "transimmunization (TI)" since the new therapy permits transfer of tumor antigens that have been previously poorly recognized to potent antigen presenting cells where the tumor epitopes can be displayed in the full context of major histocompatibility, co-stimulatory and adhesion molecules. The TI modification of ECP is a practical and safe means of rapidly inducing DC differentiation from peripheral blood monocytes in the presence of apoptotic tumor cells. Uptake of the apoptotic CTCL cells by the immature DC, in the presence of inflammatory cytokines, further drives their maturation into potent antigen presenting cells. Reinfusion of these tumor-loaded DC, that have access to the full spectrum of tumor antigens, has the potential to invoke an anti-tumor immune response in the recipient. Standard ECP has been a very useful form of immunotherapy and a modification of this approach that can enhance its efficacy and utility should broaden its application to a larger variety of disorders including potentially the treatment of solid tumors and the modulation of the immune response in graft-versus-leukemia and graft-versus-host transplantation regimens. An understanding of the mechanism of ECP and TI will provide the physician with the ability to more finely tune the desired immune response and thereby, provide an enhanced immunotherapy for malignancy and other disorders of immunocompetence. (C) 2002 Elsevier Science Ltd. All rights reserved.
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页码:205 / 216
页数:12
相关论文
共 39 条
[1]  
Abrams JT, 2001, ANN NY ACAD SCI, V941, P69
[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]   Photopheresis for the prevention of rejection in cardiac transplantation [J].
Barr, ML ;
Meiser, BM ;
Eisen, HJ ;
Roberts, RF ;
Livi, U ;
Dall'Amico, R ;
Dorent, R ;
Rogers, JG ;
Radovancevic, B ;
Taylor, DO ;
Jeevanandam, V ;
Marboe, CC ;
Franco, EL ;
Ventura, HO ;
Michler, RE ;
Griffith, BP ;
Boyce, SW ;
Reichart, B ;
Gandjbakhch, I .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (24) :1744-1751
[4]  
Berger CL, 1998, INT J CANCER, V76, P304, DOI 10.1002/(SICI)1097-0215(19980504)76:3<304::AID-IJC3>3.0.CO
[5]  
2-Z
[6]   INHIBITION OF AUTOIMMUNE-DISEASE IN A MURINE MODEL OF SYSTEMIC LUPUS-ERYTHEMATOSUS INDUCED BY EXPOSURE TO SYNGENEIC PHOTOINACTIVATED LYMPHOCYTES [J].
BERGER, CL ;
PEREZ, M ;
LAROCHE, L ;
EDELSON, R .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 94 (01) :52-57
[7]   The immune response to class I-associated tumor-specific cutaneous T-cell lymphoma antigens [J].
Berger, CL ;
Wang, N ;
Christensen, I ;
Longley, J ;
Heald, P ;
Edelson, RL .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 107 (03) :392-397
[8]  
BERGER CL, 1979, BLOOD, V53, P642
[9]  
Berger CL, 2001, INT J CANCER, V91, P438, DOI 10.1002/1097-0215(200002)9999:9999<::AID-IJC1073>3.0.CO
[10]  
2-R