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减毒单核细胞增生李斯特菌作为一种癌症疫苗载体,用于递送肝癌干细胞的生物标志物CD24。

Attenuated Listeria monocytogenes as a cancer vaccine vector for the delivery of CD24, a biomarker for hepatic cancer stem cells.

作者信息

Yang Yu, Hou Jiajie, Lin Zhe, Zhuo Han, Chen Dianyu, Zhang Xudong, Chen Yun, Sun Beicheng

机构信息

Liver Transplantation Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Department of Microbiology and Immunology, Nanjing Medical University, Nanjing, China.

出版信息

Cell Mol Immunol. 2014 Mar;11(2):184-96. doi: 10.1038/cmi.2013.64. Epub 2014 Feb 3.

Abstract

Attenuated Listeria monocytogenes (LM) is a promising candidate vector for the delivery of cancer vaccines. After phagocytosis by antigen-presenting cells, this bacterium stimulates the major histocompatibility complex (MHC)-I and MHC-II pathways and induces the proliferation of antigen-specific T lymphocytes. A new strategy involving genetic modification of the replication-deficient LM strain ΔdalΔdat (Lmdd) to express and secrete human CD24 protein has been developed. CD24 is a hepatic cancer stem cell biomarker that is closely associated with apoptosis, metastasis and recurrence of hepatocellular carcinoma (HCC). After intravenous administration in mice, Lmdd-CD24 was distributed primarily in the spleen and liver and did not cause severe organ injury. Lmdd-CD24 effectively increased the number of interferon (IFN)-γ-producing CD8(+) T cells and IFN-γ secretion. Lmdd-CD24 also enhanced the number of IL-4- and IL-10-producing T helper 2 cells. The efficacy of the Lmdd-CD24 vaccine was further investigated against Hepa1-6-CD24 tumors, which were inguinally inoculated into mice. Lmdd-CD24 significantly reduced the tumor size in mice and increased their survival. Notably, a reduction of T regulatory cell (Treg) numbers and an enhancement of specific CD8(+) T-cell activity were observed in the tumor-infiltrating lymphocytes (TILs). These results suggest a potential application of the Lmdd-CD24 vaccine against HCC.

摘要

减毒单核细胞增生李斯特菌(LM)是一种很有前景的癌症疫苗递送载体。被抗原呈递细胞吞噬后,这种细菌会刺激主要组织相容性复合体(MHC)-I和MHC-II途径,并诱导抗原特异性T淋巴细胞增殖。一种新策略已被开发出来,即对复制缺陷型LM菌株ΔdalΔdat(Lmdd)进行基因改造,使其表达并分泌人CD24蛋白。CD24是一种肝癌干细胞生物标志物,与肝细胞癌(HCC)的凋亡、转移和复发密切相关。在小鼠静脉注射后,Lmdd-CD24主要分布在脾脏和肝脏中,并未造成严重的器官损伤。Lmdd-CD24有效增加了产生干扰素(IFN)-γ的CD8(+) T细胞数量和IFN-γ分泌。Lmdd-CD24还增加了产生IL-4和IL-10的辅助性T2细胞数量。针对腹股沟接种到小鼠体内的Hepa1-6-CD24肿瘤,进一步研究了Lmdd-CD24疫苗的疗效。Lmdd-CD24显著减小了小鼠体内的肿瘤大小并提高了它们的存活率。值得注意的是,在肿瘤浸润淋巴细胞(TILs)中观察到调节性T细胞(Treg)数量减少以及特异性CD8(+) T细胞活性增强。这些结果表明Lmdd-CD24疫苗在抗HCC方面具有潜在应用价值。

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