Chemotherapy and tumor immunity: an unexpected collaboration

被引:42
作者
Emens, Leisha A. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Dept Oncol, Tumor Immunol Program, Baltimore, MD 21231 USA
[2] Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2008年 / 13卷
关键词
TRAIL; CEA; rVV; PSA; GM-CSF; CTL; TLR; LPS; tumor immunity; chemotherapy; cancer; vaccines; immune tolerance; review;
D O I
10.2741/2675
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chemotherapy directly targets the transformed tumor cell, and has long been a key component of therapy for most early and advanced cancers. However, its utility is ultimately limited by unavoidable toxicity to normal tissues, and by drug resistance pathways deeply embedded within the biology of the tumor cell itself. These limitations strongly argue for innovative strategies to treat and manage cancer. Engaging the power of the patient's own immune system is a highly attractive way to complement the activity of standard cancer treatment. Tumor vaccines offer the potential for preventing cancer in those at high risk for disease development, preventing relapse in those diagnosed with early cancer, and treating advanced disease. Notably, the barriers to tumor vaccine efficacy are distinct from the limitations of combination chemotherapy. The ability of vaccines to induce a response robust enough to mediate tumor rejection is limited by the extent of disease burden, the suppressive effect of the local tumor micronenvironment, and multiple layers of systemic immune tolerance established to keep the immune response turned off. Chemotherapy can be used with tumor vaccines in unexpected ways, breaking down these barriers and unleashing the full potential of the antitumor immune response.
引用
收藏
页码:249 / 257
页数:9
相关论文
共 73 条
[1]   A randomized phase II study of concurrent docetaxel plus vaccine versus vaccine alone in metastatic androgen-independent prostate cancer [J].
Arlen, PM ;
Gulley, JL ;
Parker, C ;
Skarupa, L ;
Pazdur, M ;
Panicali, D ;
Beetham, P ;
Tsang, KY ;
Grosenbach, DW ;
Feldman, J ;
Steinberg, SM ;
Jones, E ;
Chen, C ;
Marte, J ;
Schlom, J ;
Dahut, W .
CLINICAL CANCER RESEARCH, 2006, 12 (04) :1260-1269
[2]   Therapeutic synergy of human papillomavirus E7 subunit vaccines plus cisplatin in an animal tumor model: Causal involvement of increased sensitivity of cisplatin-treated tumors to CTL-mediated killing in therapeutic synergy [J].
Bae, Sung Hwa ;
Park, Young-Ja ;
Park, Jae-Bok ;
Choi, Youn Seok ;
Kim, Mi Suk ;
Sin, Jeong-Im .
CLINICAL CANCER RESEARCH, 2007, 13 (01) :341-349
[3]   Antigen presentation machinery (APM) modulation and soluble HLA molecules in the tumor microenvironment: Do they provide tumor cells with escape mechanisms from recognition by cytotoxic T lymphocytes? [J].
Bangia, Naveen ;
Ferrone, Soldano .
IMMUNOLOGICAL INVESTIGATIONS, 2006, 35 (3-4) :485-503
[4]   Reduced frequencies and suppressive function of CD4+CD25hi regulatory T cells in patients with chronic lymphocytic leukemia after therapy with fludarabine [J].
Beyer, M ;
Kochanek, M ;
Darabi, K ;
Popov, A ;
Jensen, M ;
Endl, E ;
Knolle, PA ;
Thomas, RK ;
von Bergwelt-Baildon, M ;
Bebey, S ;
Hallek, M ;
Schultze, JL .
BLOOD, 2005, 106 (06) :2018-2025
[5]  
Bocci G, 2002, CANCER RES, V62, P6938
[6]  
Borrello I, 2000, BLOOD, V95, P3011
[7]  
Byrd-Leifer CA, 2001, EUR J IMMUNOL, V31, P2448, DOI 10.1002/1521-4141(200108)31:8&lt
[8]  
2448::AID-IMMU2448&gt
[9]  
3.0.CO
[10]  
2-N