Immunotherapy for prostate cancer

被引:25
作者
Fong, L
Small, EJ
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Immunol Microbiol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Urol, San Francisco, CA 94143 USA
关键词
D O I
10.1016/S0093-7754(03)00350-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
While androgen deprivation has remained the cornerstone of therapy for advanced prostate cancer over the last 60 years, novel therapies are being developed that may expand upon currently available treatments. The identification of antigens expressed by prostate tissue and/or prostate cancer that are recognized by T cells creates opportunities to develop novel immunotherapeutic approaches, including tumor vaccines. Improved understanding of immune recognition and antigen presentation may lead to effective immunotherapies for prostate cancer. Identified proteins expressed in prostate cancer, including prostate-specific antigen (PSA), prostatic acid phosphatase (PAP), and prostate-specific membrane antigen (PSMA), have been used as immunologic targets for immunotherapy. Moreover, innovations in cancer genomics and proteomics will also aid in the identification of immunologic targets. Immunotherapy trials have already demonstrated evidence of not only immunogenicity, but also clinical efficacy, and future studies will be directed at capitalizing on these findings. © 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:649 / 658
页数:10
相关论文
共 61 条
[1]  
Agus DB, 1999, CANCER RES, V59, P4761
[2]   Intraperitoneal radioimmunotherapy of ovarian cancer with Lu-177-CC49: A phase I/II study [J].
Alvarez, RD ;
Partridge, EE ;
Khazaeli, MB ;
Plott, G ;
Austin, M ;
Kilgore, L ;
Russell, CD ;
Liu, TP ;
Grizzle, WE ;
Schlom, J ;
LoBuglio, AF ;
Meredith, RF .
GYNECOLOGIC ONCOLOGY, 1997, 65 (01) :94-101
[3]  
[Anonymous], P AM SOC CLIN ONCOL
[4]  
BANDER NH, 2002, P AN M AM SOC CLIN, V21, pA5
[5]   MAJOR HISTOCOMPATIBILITY COMPLEX CLASS II(+)B7-1(+) TUMOR-CELLS ARE POTENT VACCINES FOR STIMULATING TUMOR REJECTION IN TUMOR-BEARING MICE [J].
BASKAR, S ;
GLIMCHER, L ;
NABAVI, N ;
JONES, RT ;
OSTRANDROSENBERG, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (02) :619-629
[6]   In vitro generation of human cytotoxic T lymphocytes specific for peptides derived from prostate-specific antigen [J].
Correale, P ;
Walmsley, K ;
Nieroda, C ;
Zaremba, S ;
Zhu, MZ ;
Schlom, J ;
Tsang, KY .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (04) :293-300
[7]  
Dannull J, 2000, CANCER RES, V60, P5522
[8]  
DAVIS TA, 2002, P AN M AM SOC CLIN, V21, P74
[9]  
Deb N, 1996, CLIN CANCER RES, V2, P1289
[10]   VACCINATION WITH IRRADIATED TUMOR-CELLS ENGINEERED TO SECRETE MURINE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR STIMULATES POTENT, SPECIFIC, AND LONG-LASTING ANTITUMOR IMMUNITY [J].
DRANOFF, G ;
JAFFEE, E ;
LAZENBY, A ;
GOLUMBEK, P ;
LEVITSKY, H ;
BROSE, K ;
JACKSON, V ;
HAMADA, H ;
PARDOLL, D ;
MULLIGAN, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3539-3543