Developing dendritic cell polynucleotide vaccination for prostate cancer immunotherapy

被引:14
作者
Berlyn, KA
Ponniah, S
Stass, SA
Malone, JG
Hamlin-Green, G
Lim, JK
Cottler-Fox, M
Tricot, G
Alexander, RB
Mann, DL
Malone, RW
机构
[1] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[2] Univ Maryland, Greenebaum Canc Ctr, Baltimore, MD 21201 USA
[3] VA Maryland Hlth Care Syst, Baltimore, MD 21201 USA
关键词
prostate cancer; cancer immunotherapy; dendritic cells;
D O I
10.1016/S0168-1656(99)00118-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Immunotherapy has been successfully used to treat some human malignancies, principally melanoma and renal cell carcinoma. Genetic-based cancer immunotherapies were proposed which prime T lymphocyte recognition of unique neo-antigens arising from specific mutations. Genetic immunization (polynucleotide vaccination, DNA vaccines) is a process whereby gene therapy methods are used to create vaccines and immunotherapies. Recent findings indicate that genetic immunization works indirectly via a bone marrow derived cell. probably a type of dendritic antigen presenting cell (APC). Direct targeting of genetic vaccines to these cells may provide an efficient method for stimulating cellular and humoral immune responses to infectious agents and tumor antigens. Initial studies have provided monocytic-derived dendritic cell (DC) isolation and culture techniques, simple methods for delivering genes into these cells, and have also uncovered potential obstacles to effective cancer immunotherapy which may restrict the utility of this paradigm to a subset of patients. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:155 / 179
页数:25
相关论文
共 79 条
[1]  
AbdelWahab Z, 1997, CANCER, V80, P401, DOI 10.1002/(SICI)1097-0142(19970801)80:3<401::AID-CNCR8>3.0.CO
[2]  
2-U
[3]   Autoimmune prostatitis: Evidence of T cell reactivity with normal prostatic proteins [J].
Alexander, RB ;
Brady, F ;
Ponniah, S .
UROLOGY, 1997, 50 (06) :893-899
[4]   DENDRITIC CELLS GENERATED FROM PERIPHERAL-BLOOD TRANSFECTED WITH HUMAN TYROSINASE INDUCE SPECIFIC T-CELL ACTIVATION [J].
ALIJAGIC, S ;
MOLLER, P ;
ARTUC, M ;
JURGOVSKY, K ;
CZARNETZKI, BM ;
SCHADENDORF, D .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (11) :3100-3107
[5]  
Alpan RS, 1996, CANCER RES, V56, P4358
[6]   Bone marrow-generated dendritic cells pulsed with tumor extracts or tumor RNA induce antitumor immunity against central nervous system tumors [J].
Ashley, DM ;
Faiola, B ;
Nair, S ;
Hale, LP ;
Bigner, DD ;
Gilboa, E .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (07) :1177-1182
[7]   Dendritic cells process exogenous viral proteins and virus-like particles for class I presentation to CD8(+) cytotoxic T lymphocytes [J].
Bachmann, MF ;
Lutz, MB ;
Layton, GT ;
Harris, SJ ;
Fehr, T ;
Rescigno, M ;
RicciardiCastagnoli, P .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (11) :2595-2600
[8]  
Bailet JW, 1997, ARCH OTOLARYNGOL, V123, P855
[9]   LOSS OF HLA CLASS-I EXPRESSION IN PROSTATE-CANCER - IMPLICATIONS FOR IMMUNOTHERAPY [J].
BLADES, RA ;
KEATING, PJ ;
MCWILLIAM, LJ ;
GEORGE, NJR ;
STERN, PL .
UROLOGY, 1995, 46 (05) :681-686
[10]   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