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诱导抗原特异性TH9免疫并伴有肥大细胞活化可阻断肿瘤细胞植入。

Induction of antigen-specific TH 9 immunity accompanied by mast cell activation blocks tumor cell engraftment.

作者信息

Abdul-Wahid Aws, Cydzik Marzena, Prodeus Aaron, Alwash Mays, Stanojcic Mile, Thompson Megan, Huang Eric H-B, Shively John E, Gray-Owen Scott D, Gariépy Jean

机构信息

Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.

Physical Sciences, Sunnybrook Research Institute, Toronto, ON, CANADA.

出版信息

Int J Cancer. 2016 Aug 15;139(4):841-53. doi: 10.1002/ijc.30121. Epub 2016 Apr 15.

Abstract

The engraftment of circulating cancer cells at distal sites represents a key step in the metastatic cascade, yet remains an unexplored target for therapeutic intervention. In this study, we establish that a vaccination strategy yielding an antigen-specific TH 9 response induces long term host surveillance and prevents the engraftment of circulating cancer cells. Specifically, we show that vaccination with a recombinant CEA IgV-like N domain, formulated with the TLR3 ligand poly I:C, elicits a CEA-specific TH 9 response, wherein IL-9 secreting TH cells act in concert with CEA N domain-specific antibodies as well as activated mast cells in preventing tumor cell engraftment. The development of this immune response was dependent on TLR3, since interference with the TLR3-dsRNA complex formation led to a reduction in vaccine-imparted protection and a shift in the resulting immune response toward a TH 2 response. These findings point to the existence of an alternate tumor targeting immune mechanism that can be exploited for the purpose of developing vaccine therapies targeting tumor dissemination and engraftment.

摘要

循环癌细胞在远端部位的植入是转移级联反应中的关键步骤,但仍是治疗干预尚未探索的靶点。在本研究中,我们证实产生抗原特异性TH9反应的疫苗接种策略可诱导长期的宿主监测并防止循环癌细胞的植入。具体而言,我们表明用与TLR3配体聚肌胞苷酸(poly I:C)配制的重组癌胚抗原(CEA)IgV样N结构域进行疫苗接种可引发CEA特异性TH9反应,其中分泌白细胞介素-9(IL-9)的TH细胞与CEA N结构域特异性抗体以及活化的肥大细胞协同作用,防止肿瘤细胞植入。这种免疫反应的发展依赖于TLR3,因为干扰TLR3-双链RNA(dsRNA)复合物的形成会导致疫苗赋予的保护作用降低,并使产生的免疫反应转向TH2反应。这些发现表明存在一种可用于开发针对肿瘤播散和植入的疫苗疗法的替代肿瘤靶向免疫机制。

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