Prostate cancer immunotherapy yields superior long-term survival in TRAMP mice when administered at an early stage of carcinogenesis prior to the establishment of tumor-associated immunosuppression at later stages

被引:29
作者
Gray, Andrew [1 ,2 ]
Garcia-Hernandez, Maria de la Luz [1 ,2 ]
van West, Myrna [1 ,2 ]
Kanodia, Shreya [1 ,2 ]
Hubby, Bolyn [3 ]
Kast, W. Martin [1 ,2 ,4 ,5 ]
机构
[1] Univ So Calif, Dept Mol Microbiol & Immunol, Los Angeles, CA 90033 USA
[2] Univ So Calif, Kenneth Norris Jr Comprehens Canc Ctr, Los Angeles, CA 90033 USA
[3] AlphaVax Inc, Res Triangle Pk, NC USA
[4] Univ So Calif, Dept Obstet & Gynecol, Los Angeles, CA 90089 USA
[5] Univ Hawaii, Canc Res Ctr, Honolulu, HI 96813 USA
关键词
Prostate cancer; Immunotherapy; Regulatory T cells; REGULATORY T-CELLS; 6-TRANSMEMBRANE EPITHELIAL ANTIGEN; INDOLEAMINE 2,3-DIOXYGENASE; IMMUNE-RESPONSE; IN-VIVO; PERIPHERAL-BLOOD; VACCINATION; ADENOCARCINOMA; AUTOIMMUNITY; GENERATION;
D O I
10.1016/j.vaccine.2009.09.106
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Prostate cancer immunotherapy clinical trials have been performed, but often in immunocompromised patients with limited clinical success. The study aim was to determine whether the stage of prostate cancer development at which immunization occurs affects vaccine efficacy, and if so which tumor-associated immunosuppressive mechanisms may be involved at later stages. Therapeutic vaccination of TRAMP mice with only precancerous PIN lesions confered superior protection to immunization after development of invasive carcinoma. The presence of Treg, upregulation of tumor indoleamine-2,3-dioxygenase and TGF beta and an immunosuppressive intratumoral cytokine milieu were identified in more advanced prostate cancer. These results indicate that prostate cancer immunotherapy trials will be more successful if conducted in patients with less advanced disease. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:G52 / G59
页数:8
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