Advances in cellular immunotherapy for malignant melanoma

被引:0
作者
López, M
Escobar, A
Alfaro, J
Fodor, M
Larrondo, M
Ferrada, C
Salazar-Onfray, F
机构
[1] Univ Chile, Fac Med, Inst Ciencias Biomed, Disciplinario Immunol, Santiago, Chile
[2] Univ Chile, Fac Med, Inst Ciencias Biomed, Santiago, Chile
关键词
dendritic cells; immunotherapy; interleukin-2; malignant melanoma;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An alternative strategy for cancer treatment is the main manipulation of the immune system, denominated cancer immunotherapy. The immunotherapeutical use of cells of the immune system, like dendritic cells (DC), is being explored in different clinical protocols. Recently, we finalized a clinical phase I protocol, for the treatment of malignant melanoma, using DC's loaded with tumor lysates. Our results indicate that the subcutaneous application of DC's do not produce adverse effects. We also observed an increase of tumor specific T lymphocytes precursors in the blood, associated to hypersensitivity reactions (DTH) in 60% of the treated patients. In most cases, an stability in the disease was observed, although without a significant association between vaccination and survival. Additionally, therapies based in Interleukin-2 (IL-2) have been used with relative success in the treatment of some kind of tumors since 1985. However, problems associated to the toxicity of IL-2 still restrict its massive use. Our direct experience with the use if IL-2 indicates that low doses and its subcutaneous application, maintains the beneficial effects for patients, eliminating the adverse effects. Based on the accumulated evidence during last the five years, we decided to implement an optimized clinical protocol, which alternatively combines dendritic cells vaccines with the use of low doses of IL-2 for the immunological system.
引用
收藏
页码:1115 / 1126
页数:12
相关论文
共 80 条
[1]   Immature dendritic cells phagocytose apoptotic cells via αvβ5 and CD36, and cross-present antigens to cytotoxic T lymphocytes [J].
Albert, ML ;
Pearce, SFA ;
Francisco, LM ;
Sauter, B ;
Roy, P ;
Silverstein, RL ;
Bhardwaj, N .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (07) :1359-1368
[2]   Interleukin-2: Clinical applications [J].
Atkins, MB .
SEMINARS IN ONCOLOGY, 2002, 29 (03) :12-17
[3]   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-+
[4]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[5]   INTERFERON-GAMMA AND TUMOR-NECROSIS-FACTOR HAVE A ROLE IN TUMOR REGRESSIONS MEDIATED BY MURINE CD8+ TUMOR-INFILTRATING LYMPHOCYTES [J].
BARTH, RJ ;
MULE, JJ ;
SPIESS, PJ ;
ROSENBERG, SA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (03) :647-658
[6]   Dendritic cells pulsed with RNA are potent antigen-presenting cells in vitro and in vivo [J].
Boczkowski, D ;
Nair, SK ;
Snyder, D ;
Gilboa, E .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :465-472
[7]  
BOON T, 1994, ANNU REV IMMUNOL, V12, P337, DOI 10.1146/annurev.iy.12.040194.002005
[8]   FROM DEFINED HUMAN TUMOR-ANTIGENS TO EFFECTIVE IMMUNIZATION [J].
BOON, T ;
GAJEWSKI, TF ;
COULIE, PG .
IMMUNOLOGY TODAY, 1995, 16 (07) :334-336
[9]   THE TYROSINASE GENE CODES FOR AN ANTIGEN RECOGNIZED BY AUTOLOGOUS CYTOLYTIC T-LYMPHOCYTES ON HLA-A2 MELANOMAS [J].
BRICHARD, V ;
VANPEL, A ;
WOLFEL, T ;
WOLFEL, C ;
DEPLAEN, E ;
LETHE, B ;
COULIE, P ;
BOON, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (02) :489-495
[10]   MOLECULAR-CLONING AND EXPRESSION OF THE HUMAN MELANOCYTE STIMULATING HORMONE RECEPTOR CDNA [J].
CHHAJLANI, V ;
WIKBERG, JES .
FEBS LETTERS, 1992, 309 (03) :417-420