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用非复制型弓形虫尿嘧啶营养缺陷型疫苗靶向肿瘤。

Targeting tumors with nonreplicating Toxoplasma gondii uracil auxotroph vaccines.

机构信息

Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, 1 Medical Center Drive, Lebanon, NH 03756, USA.

出版信息

Trends Parasitol. 2013 Sep;29(9):431-7. doi: 10.1016/j.pt.2013.07.001. Epub 2013 Aug 5.

Abstract

Toxoplasma gondii is an intracellular parasite that has evolved to actively control its invaded host cells. Toxoplasma triggers then actively regulates host innate interleukin-12 (IL-12) and interferon-γ (IFN-γ) responses that elicit T cell control of infection. A live, nonreplicating avirulent uracil auxotroph vaccine strain (cps) of Toxoplasma triggers novel innate immune responses that stimulate amplified CD8(+) T cell responses and life-long immunity in vaccinated mice. Here, we review recent reports showing that intratumoral treatment with cps activated immune-mediated regression of established solid tumors in mice. We speculate that a better understanding of host-parasite interaction at the molecular level and applying improved genetic models based on Δku80 Toxoplasma strains will stimulate development of highly effective immunotherapeutic cancer vaccine strategies using engineered uracil auxotrophs.

摘要

刚地弓形虫是一种细胞内寄生虫,它已经进化到能够主动控制被入侵的宿主细胞。弓形虫触发并主动调节宿主先天的白细胞介素-12(IL-12)和干扰素-γ(IFN-γ)反应,从而引发 T 细胞对感染的控制。一种活的、非复制的无毒尿嘧啶营养缺陷型疫苗株(cps)可以触发新的先天免疫反应,刺激 CD8(+)T 细胞反应的放大,并在接种疫苗的小鼠中产生终身免疫。在这里,我们回顾了最近的报告,表明 cps 经肿瘤内治疗可激活免疫介导的已建立的实体肿瘤消退。我们推测,更好地理解宿主-寄生虫在分子水平上的相互作用,并应用基于 Δku80 弓形虫株的改进的遗传模型,将刺激使用工程化尿嘧啶营养缺陷型的高效免疫治疗癌症疫苗策略的发展。

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Toxoplasma co-opts host cells it does not invade.刚地弓形虫会利用它不入侵的宿主细胞。
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