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重组腺病毒AdmIL-12介导的光动力疗法增强了人乳头瘤病毒16(E6/E7)感染肿瘤模型中的抗肿瘤治疗效果。

Photodynamic therapy with recombinant adenovirus AdmIL-12 enhances anti-tumour therapy efficacy in human papillomavirus 16 (E6/E7) infected tumour model.

作者信息

Park Eun Kyung, Bae Su-Mi, Kwak Sun-Young, Lee Sung Jong, Kim Yong-Wook, Han Chan-Hee, Cho Hyun-Jung, Kim Kyung Tae, Kim Young-Jae, Kim Hyun-Jung, Ahn Woong Shick

机构信息

Department of Obstetrics and Gynecology, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

Immunology. 2008 Aug;124(4):461-8. doi: 10.1111/j.1365-2567.2007.02797.x. Epub 2008 Apr 4.

Abstract

Immunotherapy with photodynamic therapy (PDT) offers great promise as a new alternative for cancer treatment; however, its use remains experimental. Here we investigated the utility of adenoviral delivery of interleukin-12 (AdmIL-12) as an adjuvant for PDT in mouse tumour challenge model. PDT was performed by irradiating Radachlorin in C57BL/6 mice transplanted with TC-1 cells. PDT plus AdmIL-12 treatment for tumour suppression as well as specific immune responses were evaluated with the following tests: in vitro and in vivo tumour growth inhibition, interferon-gamma (IFN-gamma) and tumour necrosis factor-alpha (TNF-alpha) assay, and cytotoxic T lymphocyte (CTL) assay. Direct intratumoral injection of AdmIL-12 resulted in a significant suppression of tumour growth compared to the control group. Treatment of PDT along with AdmIL-12 further enhanced antitumour effects significantly higher than either AdmIL-12 or PDT alone. This combined treatment resulted in complete regression of 9-mm sized tumour in every animal. We also evaluated immune responses induced by these treatments. Combined treatment significantly increased the production level of IFN-gamma and TNF-alpha compared with that by AdmIL-12 or PDT alone. PDT plus AdmIL-12 enhanced antitumour immunity through increased expansion of the CTL subset mediated by CD8+ T cells. Taken together, these results indicate that the high anti-cancer activity of PDT with AdmIL-12 is a powerful tool against cancer therapy and is a promising subject for further investigation.

摘要

光动力疗法(PDT)免疫疗法作为一种癌症治疗的新选择具有很大的前景;然而,其应用仍处于实验阶段。在这里,我们在小鼠肿瘤攻击模型中研究了腺病毒介导的白细胞介素-12(AdmIL-12)作为PDT佐剂的效用。通过照射移植了TC-1细胞的C57BL/6小鼠体内的拉达氯林来进行PDT。通过以下测试评估PDT加AdmIL-12治疗对肿瘤抑制以及特异性免疫反应的效果:体外和体内肿瘤生长抑制、干扰素-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)测定以及细胞毒性T淋巴细胞(CTL)测定。与对照组相比,直接瘤内注射AdmIL-12导致肿瘤生长显著受到抑制。PDT与AdmIL-12联合治疗进一步显著增强了抗肿瘤效果,明显高于单独使用AdmIL-12或PDT。这种联合治疗使每只动物体内9毫米大小的肿瘤完全消退。我们还评估了这些治疗诱导的免疫反应。与单独使用AdmIL-12或PDT相比,联合治疗显著提高了IFN-γ和TNF-α的产生水平。PDT加AdmIL-12通过增加由CD8 + T细胞介导的CTL亚群的扩增来增强抗肿瘤免疫力。综上所述,这些结果表明,PDT与AdmIL-12的高抗癌活性是对抗癌症治疗的有力工具,并且是进一步研究的有希望的课题。

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