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开发一种重组异种肿瘤坏死因子α蛋白疫苗以保护小鼠免受实验性结肠炎的侵害。

Development of a Recombinant Xenogeneic Tumor Necrosis Factor Alpha Protein Vaccine To Protect Mice from Experimental Colitis.

作者信息

Wan Yang, Li Meng, Zhang Hailong, Zheng Xiuran, Yu Chaoheng, He Gu, Luo Yan, Yang Li, Wei Yuquan

机构信息

Department of Geriatric Medicine, No. 4 West China Teaching Hospital, Sichuan University, Chengdu, People's Republic of China State Key Laboratory of Biotherapy/Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, People's Republic of China.

State Key Laboratory of Biotherapy/Collaborative Innovation Center for Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, People's Republic of China.

出版信息

Clin Vaccine Immunol. 2015 Dec;22(12):1269-75. doi: 10.1128/CVI.00331-15. Epub 2015 Oct 14.

Abstract

Previous studies have highlighted the efficacy of tumor necrosis factor alpha (TNF-α) inhibitors, including monoclonal antibodies and soluble receptors, in the treatment and management of intestinal bowel disease (IBD). However, because of the immunogenicity of xenogeneic TNF-α inhibitors, antidrug antibodies (ADAs) can be triggered after repeated administration. An alternative way to target TNF-α is active immunization to elicit the production of high titers of neutralizing antibodies. In this study, we prepared a xenogeneic TNF-α protein vaccine and studied the protective effects in experimental colitis models. The xenogeneic TNF-α protein vaccine could overcome self-tolerance and induce TNF-α-specific neutralizing antibody. Moreover, the xenogeneic TNF-α protein vaccine could protect mice from acute and chronic colitis induced by dextran sodium sulfate (DSS). One possible explanation for this protective effect is the production of TNF-α-specific neutralizing antibody, which absorbed the biological activity of mouse TNF-α (mTNF-α) and failed to induce T lymphocyte apoptosis. In summary, use of the xenogeneic TNF-α protein vaccine may be a potent therapeutic strategy for IBD.

摘要

先前的研究强调了肿瘤坏死因子α(TNF-α)抑制剂(包括单克隆抗体和可溶性受体)在治疗和管理炎症性肠病(IBD)方面的疗效。然而,由于异种TNF-α抑制剂具有免疫原性,重复给药后可能会引发抗药物抗体(ADA)。靶向TNF-α的另一种方法是主动免疫,以引发高滴度中和抗体的产生。在本研究中,我们制备了一种异种TNF-α蛋白疫苗,并研究了其在实验性结肠炎模型中的保护作用。异种TNF-α蛋白疫苗可以克服自身耐受性并诱导TNF-α特异性中和抗体。此外,异种TNF-α蛋白疫苗可以保护小鼠免受葡聚糖硫酸钠(DSS)诱导的急性和慢性结肠炎的影响。这种保护作用的一种可能解释是产生了TNF-α特异性中和抗体,该抗体吸收了小鼠TNF-α(mTNF-α)的生物活性,未能诱导T淋巴细胞凋亡。总之,使用异种TNF-α蛋白疫苗可能是治疗IBD的有效策略。

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本文引用的文献

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Nat Rev Immunol. 2014 May;14(5):329-42. doi: 10.1038/nri3661. Epub 2014 Apr 22.
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