Impediments to successful immunotherapy

被引:34
作者
Hersey, P [1 ]
机构
[1] CNR, Immunol & Oncol Unit, Newcastle, NSW 2300, Australia
关键词
anergy; antigen loss; suppressive factors; resistance to apoptosis; T-cell migration; therapeutic strategies;
D O I
10.1016/S0163-7258(98)00038-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Over the last decade, there has been a considerable increase in understanding of immune responses against cancers, the antigenic structures on tumor cells recognised by the immune system, and the development of more effective vaccines. There is, however, very limited understanding of why the immune system most often fails to control tumor growth and progression. In some patients, it is difficult to demonstrate immune responses to their tumors, and it may be assumed that this reflects poor recognition of tumor antigens, induction of anergy in lymphocytes, or suppression of immune responses by tumor derived factors, In other patients, tumor progression appears to occur despite the presence of antibody or cell-mediated responses, This may indicate selection of tumor cells that have lost tumor antigens or HLA antigens by immune responses against the tumor. Tumor cells may also become resistant to mediators of apoptosis, such as Fas ligand and tumor necrosis factor related apoptosis-inducing ligand used by lymphocytes to kill tumor cells. It is suggested that development of effective immunotherapy will need to include strategies that rake into account these limitations of immune responses and classification of tumors according to the treatment approach most likely to succeed. PHARMACOL THER 81(2):111-119, 1999. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:111 / 119
页数:9
相关论文
共 95 条
[71]  
RIVOLTINI L, 1995, CANCER RES, V55, P3149
[72]   Selective expression of an interleukin-12 receptor component by human T helper 1 cells [J].
Rogge, L ;
BarberisMaino, L ;
Biffi, M ;
Passini, N ;
Presky, DH ;
Gubler, U ;
Sinigaglia, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (05) :825-831
[73]  
Rokhlin OW, 1997, CANCER RES, V57, P1758
[74]   MODULATION OF T-CELL FUNCTION BY GLIOMAS [J].
ROSZMAN, T ;
ELLIOTT, L ;
BROOKS, W .
IMMUNOLOGY TODAY, 1991, 12 (10) :370-374
[75]   FACTORS, INCLUDING TRANSFORMING GROWTH-FACTOR-BETA, RELEASED IN THE GLIOBLASTOMA RESIDUAL CAVITY, IMPAIR ACTIVITY OF ADHERENT LYMPHOKINE-ACTIVATED KILLER-CELLS [J].
RUFFINI, PA ;
RIVOLTINI, L ;
SILVANI, A ;
BOIARDI, A ;
PARMIANI, G .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 1993, 36 (06) :409-416
[76]  
Salvadori S, 1996, J IMMUNOL, V156, P2927
[77]   PROOPIOMELANOCORTIN-DERIVED PEPTIDES ARE SYNTHESIZED AND RELEASED BY HUMAN KERATINOCYTES [J].
SCHAUER, E ;
TRAUTINGER, F ;
KOCK, A ;
SCHWARZ, A ;
BHARDWAJ, R ;
SIMON, M ;
ANSEL, JC ;
SCHWARZ, T ;
LUGER, TA .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (05) :2258-2262
[78]   IN-SITU ANALYSIS OF TRANSFORMING GROWTH FACTOR-BETA-S (TGF-BETA-1, TGF-BETA-2, TGF-BETA-3), AND TGF-BETA TYPE-II RECEPTOR EXPRESSION IN MALIGNANT-MELANOMA [J].
SCHMID, P ;
ITIN, P ;
RUFLI, T .
CARCINOGENESIS, 1995, 16 (07) :1499-1503
[79]   TAP off - Tumors on [J].
Seliger, B ;
Maeurer, MJ ;
Ferrone, S .
IMMUNOLOGY TODAY, 1997, 18 (06) :292-299
[80]   STROMA IS CRITICAL FOR PREVENTING OR PERMITTING IMMUNOLOGICAL DESTRUCTION OF ANTIGENIC CANCER-CELLS [J].
SINGH, S ;
ROSS, SR ;
ACENA, M ;
ROWLEY, DA ;
SCHREIBER, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (01) :139-146