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荧光蛋白诱导免疫产生的含肿瘤抗原的微粒的体内可视化。

In Vivo Visualization of Tumor Antigen-containing Microparticles Generated in Fluorescent-protein-elicited Immunity.

机构信息

1. Britton Chance Center for Biomedical Photonics, Wuhan National Laboratory for Optoelectronics-Huazhong University of Science and Technology, Wuhan 430074, China;; 2. MoE Key Laboratory for Biomedical Photonics, Department of Biomedical Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.

出版信息

Theranostics. 2016 Jun 16;6(9):1453-66. doi: 10.7150/thno.14145. eCollection 2016.

Abstract

In vivo optical spatio-temporal imaging of the tumor microenvironment is useful to explain how tumor immunotherapies work. However, the lack of fluorescent antigens with strong immunogenicity makes it difficult to study the dynamics of how tumors are eliminated by any given immune response. Here, we develop an effective fluorescent model antigen based on the tetrameric far-red fluorescent protein KatushkaS158A (tfRFP), which elicits both humoral and cellular immunity. We use this fluorescent antigen to visualize the dynamic behavior of immunocytes as they attack and selectively eliminate tfRFP-expressing tumors in vivo; swarms of immunocytes rush toward tumors with high motility, clusters of immunocytes form quickly, and numerous antigen-antibody complexes in the form of tfRFP(+) microparticles are generated in the tumor areas and ingested by macrophages in the tumor microenvironment. Therefore, tfRFP, as both a model antigen and fluorescent reporter, is a useful tool to visualize specific immune responses in vivo.

摘要

肿瘤微环境的体内光学时空成像有助于解释肿瘤免疫疗法的作用机制。然而,缺乏具有强免疫原性的荧光抗原,使得研究特定免疫反应如何消除肿瘤的动态过程变得困难。在这里,我们基于四聚体远红色荧光蛋白 KatushkaS158A(tfRFP)开发了一种有效的荧光模型抗原,该抗原可引发体液和细胞免疫。我们使用这种荧光抗原来可视化免疫细胞在体内攻击和选择性消除表达 tfRFP 的肿瘤时的动态行为;免疫细胞群以高迁移率冲向肿瘤,免疫细胞簇迅速形成,并且在肿瘤区域形成大量以 tfRFP(+)微粒形式存在的抗原-抗体复合物,并被肿瘤微环境中的巨噬细胞吞噬。因此,tfRFP 作为模型抗原和荧光报告物,是可视化体内特定免疫反应的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e08c/4924512/928340a7311f/thnov06p1453g001.jpg

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