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前列腺癌免疫学:生物学、治疗方法及挑战

Prostate cancer immunology: biology, therapeutics, and challenges.

作者信息

Webster W Scott, Small Eric J, Rini Brian I, Kwon Eugene D

机构信息

Department of Urology, Mayo Clinic and Mayo Medical School, 200 1st St SW, Rochester, MN 55905, USA.

出版信息

J Clin Oncol. 2005 Nov 10;23(32):8262-9. doi: 10.1200/JCO.2005.03.4595.

DOI:10.1200/JCO.2005.03.4595
PMID:16278482
Abstract

A number of recently developed and promising approaches to antitumoral immunotherapy are being investigated as potential treatments for advanced prostate cancer. These approaches largely revolve around strategies to increase antigen-specific T-cell activation against prostate tumors as well as precise manipulations of critical co-regulatory receptors that help to maintain and prolong the activity of antigen-presenting cells and T cells that are capable of mediating tumor regression. Herein, we describe the experience with the most recent and promising approaches pertaining to prostate cancer immunotherapy. Additionally, we discuss the mechanistic basis for these approaches as well as current limitations that must still be addressed in order to propel immunotherapy into the forefront of prostate cancer treatment.

摘要

一些最近开发且前景看好的抗肿瘤免疫疗法正作为晚期前列腺癌的潜在治疗方法进行研究。这些方法主要围绕增强针对前列腺肿瘤的抗原特异性T细胞活化的策略,以及对关键共调节受体的精确操控,这些受体有助于维持和延长能够介导肿瘤消退的抗原呈递细胞和T细胞的活性。在此,我们描述了前列腺癌免疫疗法中最新且最具前景的方法的经验。此外,我们讨论了这些方法的机制基础以及为将免疫疗法推向前列腺癌治疗前沿仍需解决的当前局限性。

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1
Prostate cancer immunology: biology, therapeutics, and challenges.前列腺癌免疫学:生物学、治疗方法及挑战
J Clin Oncol. 2005 Nov 10;23(32):8262-9. doi: 10.1200/JCO.2005.03.4595.
2
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[State of the art about new therapeutic vaccines in prostate cancer: dendritic cells, engineered tumor cells and recombinant virus].[前列腺癌新型治疗性疫苗的研究现状:树突状细胞、工程化肿瘤细胞和重组病毒]
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Current immunotherapeutic strategies in prostate cancer.前列腺癌的当前免疫治疗策略。
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Treatment of biochemical recurrence of prostate cancer with granulocyte-macrophage colony-stimulating factor secreting, allogeneic, cellular immunotherapy.采用分泌粒细胞巨噬细胞集落刺激因子的异基因细胞免疫疗法治疗前列腺癌生化复发
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[Immunotherapy of prostate cancer].[前列腺癌的免疫疗法]
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Immunotherapy for prostate cancer using prostatic acid phosphatase loaded antigen presenting cells.使用负载前列腺酸性磷酸酶的抗原呈递细胞进行前列腺癌免疫治疗。
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Dendritic cell vaccines for the treatment of prostate cancer.用于治疗前列腺癌的树突状细胞疫苗。
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Granulocyte-macrophage colony-stimulating factor-transduced allogeneic cancer cellular immunotherapy: the GVAX vaccine for prostate cancer.粒细胞-巨噬细胞集落刺激因子转导的同种异体癌症细胞免疫疗法:用于前列腺癌的GVAX疫苗。
Urol Oncol. 2006 Sep-Oct;24(5):419-24. doi: 10.1016/j.urolonc.2005.08.021.

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Emerging photodynamic/sonodynamic therapies for urological cancers: progress and challenges.新兴的光动力/声动力疗法治疗泌尿系统癌症:进展与挑战。
J Nanobiotechnology. 2022 Oct 4;20(1):437. doi: 10.1186/s12951-022-01637-w.
2
Prostate Cancer Immunotherapy: Exploiting the HLA Class II Pathway in Vaccine Design.前列腺癌免疫疗法:在疫苗设计中利用HLA II类途径
J Clin Cell Immunol. 2015 Aug;6(4). doi: 10.4172/2155-9899.1000351. Epub 2015 Aug 26.
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Emerging vaccine therapy approaches for prostate cancer.前列腺癌的新型疫苗治疗方法。
Rev Urol. 2010 Winter;12(1):25-34.
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Mesenchymal stem cells modified to express lentivirus TNF-α Tumstatin(45-132) inhibit the growth of prostate cancer.转染慢病毒 TNF-α Tumstatin(45-132)的间充质干细胞抑制前列腺癌的生长。
J Cell Mol Med. 2011 Feb;15(2):433-44. doi: 10.1111/j.1582-4934.2009.00920.x.
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RHAMM (CD168) is overexpressed at the protein level and may constitute an immunogenic antigen in advanced prostate cancer disease.RHAMM(CD168)在蛋白质水平上过度表达,可能在晚期前列腺癌疾病中构成一种免疫原性抗原。
Neoplasia. 2009 Sep;11(9):956-63. doi: 10.1593/neo.09694.
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Novel targeted therapeutics for metastatic castration-resistant prostate cancer.转移性去势抵抗性前列腺癌的新型靶向治疗药物。
Cancer Lett. 2010 May 1;291(1):1-13. doi: 10.1016/j.canlet.2009.08.012. Epub 2009 Aug 29.
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Cancer gene therapy using mesenchymal stem cells expressing interferon-beta in a mouse prostate cancer lung metastasis model.在小鼠前列腺癌肺转移模型中使用表达β干扰素的间充质干细胞进行癌症基因治疗。
Gene Ther. 2008 Nov;15(21):1446-53. doi: 10.1038/gt.2008.101. Epub 2008 Jul 3.
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Current standard and investigational approaches to the management of hormone-refractory prostate cancer.激素难治性前列腺癌管理的当前标准及研究方法。
Rev Urol. 2007;9 Suppl 1(Suppl 1):S9-S19.