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超声引导下肿瘤内注射联合免疫疗法可治愈原位前列腺癌小鼠。

Ultrasound-guided intra-tumor injection of combined immunotherapy cures mice from orthotopic prostate cancer.

机构信息

Molecular Immunology Unit, Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale Tumori, Via Amadeo 42, 20133, Milan, Italy.

出版信息

Cancer Immunol Immunother. 2013 Dec;62(12):1811-9. doi: 10.1007/s00262-013-1486-7. Epub 2013 Oct 18.

Abstract

Intra-tumor injection of immunotherapeutic agents is often the most effective, likely because of concomitant modification of tumor microenvironment. We tested an immunotherapeutic regimen consisting of CpG oligonucleotides and of adenovirus-mediated gene delivery of CCL16 chemokine directly into orthotopically implanted prostate tumors by ultrasound-guided injection, followed by systemic administration of an anti-IL-10R antibody. This combination treatment induced rapid stromal rearrangement, characterized by massive leukocyte infiltration and large areas of necrosis, a scenario that eventually led to complete tumor rejection and systemic immunity in 75 % of the treated mice. In vivo T lymphocyte depletion experiments demonstrated that the efficacy of CCL16/CpG/anti-IL-10R combination treatment relies upon CD8 T lymphocytes whereas CD4 T cells are dispensable. The results underlie the feasibility of echo-guided local immunotherapy of tumors located in visceral organs that are not easily accessible.

摘要

肿瘤内注射免疫治疗药物通常是最有效的,这可能是因为同时改变了肿瘤微环境。我们通过超声引导注射,将包含 CpG 寡核苷酸和 CCL16 趋化因子的腺病毒介导的基因递送至原位植入的前列腺肿瘤中,测试了一种免疫治疗方案,然后全身性给予抗 IL-10R 抗体。这种联合治疗方案诱导了快速的基质重排,表现为大量白细胞浸润和大面积坏死,最终导致 75%的治疗小鼠完全排斥肿瘤并产生全身性免疫。体内 T 淋巴细胞耗竭实验表明,CCL16/CpG/抗 IL-10R 联合治疗的疗效依赖于 CD8 T 淋巴细胞,而 CD4 T 细胞则是可有可无的。这些结果为在不易接近的内脏器官中进行超声引导的局部肿瘤免疫治疗提供了可行性依据。

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Prostate cancer, tumor immunity and a renewed sense of optimism in immunotherapy.前列腺癌、肿瘤免疫与免疫治疗的新乐观主义
Cancer Immunol Immunother. 2012 Apr;61(4):453-68. doi: 10.1007/s00262-012-1216-6. Epub 2012 Feb 14.
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Mechanisms of immune evasion by tumors.肿瘤免疫逃逸机制
Adv Immunol. 2006;90:51-81. doi: 10.1016/S0065-2776(06)90002-9.

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