Title of article
Androgen ablation mitigates tolerance to a prostate/prostate cancer-restricted antigen
Author/Authors
Drake، نويسنده , , Charles G. and Doody، نويسنده , , Amy D.H. and Mihalyo، نويسنده , , Marianne A. and Huang، نويسنده , , Ching-Tai and Kelleher، نويسنده , , Erin and Ravi، نويسنده , , Sowmya and Hipkiss، نويسنده , , Edward L. and Flies، نويسنده , , Dallas B. and Kennedy، نويسنده , , Eugene P. and Long، نويسنده , , Meixiao and McGary، نويسنده , , Patrick W. and Coryell، نويسنده , , Lee and Nelson، نويسنده , , William G. and Pardoll، نويسنده , , Drew M. and Adler، نويسنده , , Adam J.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2005
Pages
11
From page
239
To page
249
Abstract
Summary
erstand the T cell response to prostate cancer, we created transgenic mice that express a model antigen in a prostate-restricted pattern and crossed these animals to TRAMP mice that develop spontaneous prostate cancer. Adoptive transfer of prostate-specific CD4 T cells shows that, in the absence of prostate cancer, the prostate gland is mostly ignored. Tumorigenesis allows T cell recognition of the prostate gland—but this recognition is tolerogenic, resulting in abortive proliferation and ultimately in hyporesponsiveness at the systemic level. Androgen ablation (the most common treatment for metastatic prostate cancer) was able to mitigate this tolerance—allowing prostate-specific T cells to expand and develop effector function after vaccination. These results suggest that immunotherapy for prostate cancer may be most efficacious when administered after androgen ablation.
Journal title
Cancer Cell
Serial Year
2005
Journal title
Cancer Cell
Record number
1335605
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