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卵巢癌的细胞免疫疗法。

Cellular immunotherapy for ovarian cancer.

作者信息

Cannon Martin J, O'Brien Timothy J

机构信息

University of Arkansas for Medical Sciences, Department of Microbiology and Immunology, 4301 West Markham, Little Rock, AR 72205, USA.

出版信息

Expert Opin Biol Ther. 2009 Jun;9(6):677-88. doi: 10.1517/14712590902932897.

DOI:10.1517/14712590902932897
PMID:19456205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2718679/
Abstract

BACKGROUND

Ovarian cancer is frequently diagnosed at an advanced stage, and although initially responsive to surgery and chemotherapy, has a high rate of recurrence and mortality. Cellular immunotherapy may offer the prospect of treatment to prevent or delay recurrent metastatic disease.

OBJECTIVE

To provide an overview of current innovations in cellular immunotherapy for ovarian cancer, with an emphasis on dendritic cell vaccination and adoptive T-cell immunotherapy.

METHODS

Three key areas are explored in this review: first, an appraisal of the current state of the art of cellular immunotherapy for treatment of ovarian cancer; second, a discussion of the immunological defenses erected by ovarian cancer to prevent immunological attack, with an emphasis on the role of tumor-associated regulatory T cells; and third, an exploration of innovative techniques that may enhance the ability of cellular immunotherapy to overcome ovarian tumor-associated immune suppression.

RESULTS/CONCLUSION: Ovarian cancer is recognized as a paradigm for tumor-associated immune suppression. Innovative approaches for antagonism of tumor-associated regulatory T-cell infiltration and redirection of self antigen-driven regulatory T-cell activation may provide the key to development of future strategies for cellular immunotherapy against ovarian cancer.

摘要

背景

卵巢癌常常在晚期才被诊断出来,尽管其最初对手术和化疗有反应,但复发率和死亡率很高。细胞免疫疗法可能为预防或延缓复发性转移性疾病提供治疗前景。

目的

概述卵巢癌细胞免疫疗法的当前创新,重点是树突状细胞疫苗接种和过继性T细胞免疫疗法。

方法

本综述探讨了三个关键领域:第一,评估卵巢癌细胞免疫疗法的当前技术水平;第二,讨论卵巢癌建立的免疫防御以防止免疫攻击,重点是肿瘤相关调节性T细胞的作用;第三,探索可能增强细胞免疫疗法克服卵巢肿瘤相关免疫抑制能力的创新技术。

结果/结论:卵巢癌被认为是肿瘤相关免疫抑制的范例。对抗肿瘤相关调节性T细胞浸润和重新引导自身抗原驱动的调节性T细胞活化的创新方法可能是未来卵巢癌细胞免疫治疗策略发展的关键。

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本文引用的文献

1
Beyond chemotherapy: targeted therapies in ovarian cancer.超越化疗:卵巢癌的靶向治疗
Nat Rev Cancer. 2009 Mar;9(3):167-81. doi: 10.1038/nrc2583.
2
Control of large, established tumor xenografts with genetically retargeted human T cells containing CD28 and CD137 domains.利用含有CD28和CD137结构域的基因重定向人T细胞控制大型、已形成的肿瘤异种移植瘤。
Proc Natl Acad Sci U S A. 2009 Mar 3;106(9):3360-5. doi: 10.1073/pnas.0813101106. Epub 2009 Feb 11.
3
Autoimmunity in dry eye is due to resistance of Th17 to Treg suppression.干眼症中的自身免疫是由于辅助性T细胞17(Th17)对调节性T细胞(Treg)抑制作用的抵抗。
J Immunol. 2009 Feb 1;182(3):1247-52. doi: 10.4049/jimmunol.182.3.1247.
4
Attenuated expression of A20 markedly increases the efficacy of double-stranded RNA-activated dendritic cells as an anti-cancer vaccine.A20的表达减弱显著提高了双链RNA激活的树突状细胞作为抗癌疫苗的功效。
J Immunol. 2009 Jan 15;182(2):860-70. doi: 10.4049/jimmunol.182.2.860.
5
Imatinib mesylate inhibits CD4+ CD25+ regulatory T cell activity and enhances active immunotherapy against BCR-ABL- tumors.甲磺酸伊马替尼抑制CD4+ CD25+调节性T细胞活性,并增强针对BCR-ABL肿瘤的主动免疫治疗。
J Immunol. 2008 Nov 15;181(10):6955-63. doi: 10.4049/jimmunol.181.10.6955.
6
Generation of CA125-specific cytotoxic T lymphocytes in human leukocyte antigen-A2.1-positive healthy donors and patients with advanced ovarian cancer.在人类白细胞抗原-A2.1阳性的健康供体和晚期卵巢癌患者中产生CA125特异性细胞毒性T淋巴细胞。
Am J Obstet Gynecol. 2009 Jan;200(1):75.e1-10. doi: 10.1016/j.ajog.2008.08.014. Epub 2008 Oct 30.
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Depletion of dendritic cells delays ovarian cancer progression by boosting antitumor immunity.树突状细胞的耗竭通过增强抗肿瘤免疫力来延缓卵巢癌进展。
Cancer Res. 2008 Sep 15;68(18):7684-91. doi: 10.1158/0008-5472.CAN-08-1167. Epub 2008 Sep 3.
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Reprogrammed FoxP3+ T regulatory cells become IL-17+ antigen-specific autoimmune effectors in vitro and in vivo.重编程的FoxP3+调节性T细胞在体内外均可成为IL-17+抗原特异性自身免疫效应细胞。
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J Immunol. 2008 Aug 1;181(3):1908-16. doi: 10.4049/jimmunol.181.3.1908.
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Cancer Res. 2008 Jul 15;68(14):5972-8. doi: 10.1158/0008-5472.CAN-07-6818.