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Infiltrating CTLs in Human Glioblastoma Establish Immunological Synapses with Tumorigenic Cells

机译:在人胶质母细胞瘤中浸润的CTL与致瘤细胞建立免疫突触。

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摘要

The immunological synapse between T cells and tumor cells is believed to be important for effective tumor clearance. However, the immunological synapse has never been imaged or analyzed in detail in human tissue. In this work, intercellular interactions between T cells and tumor cells were analyzed in detail in human glioblastoma. After characterization of the population of infiltrating T cells by multiple immunofluorescence staining and stereological quantification, the microanatomy of T cell-tumor cell intercellular communication was analyzed in detail using confocal microscopy and three-dimensional rendering. Cytotoxic T lymphocytes that infiltrated human glioblastoma underwent rearrangement when in contact with tumor cells, to form a three-dimensional structure in the intercellular contact area; this was characterized by microclusters of the CD3/TCR complex, re-arrangement of the cytoskeleton, and granzyme B polarization. In addition, such T cell-targeted cells show fragmentation of the microtubular system and increased expression levels of cleaved caspase 3, which suggests that cytotoxic T lymphocytes likely provoke changes in tumor cells and subsequently induce cell death. These results show that the formation of the cytotoxic T lymphocyte immunological synapse occurs in human tissue and may be relevant for the effective immune-mediated clearance of tumorigenic cells, therefore opening up new avenues for glioblastoma immunotherapy.
机译:T细胞和肿瘤细胞之间的免疫突触被认为对于有效清除肿瘤很重要。但是,从未在人体组织中对免疫突触进行成像或详细分析。在这项工作中,在人胶质母细胞瘤中详细分析了T细胞与肿瘤细胞之间的细胞间相互作用。在通过多次免疫荧光染色和立体定量表征浸润的T细胞的群体后,使用共聚焦显微镜和三维渲染技术详细分析了T细胞-肿瘤细胞间通讯的显微解剖。当浸润人胶质母细胞瘤的细胞毒性T淋巴细胞与肿瘤细胞接触时会发生重排,在细胞间接触区域形成三维结构。其特征是CD3 / TCR复合物的微簇,细胞骨架的重新排列和粒酶B极化。另外,这种靶向T细胞的细胞表现出微管系统的碎裂和裂解的半胱天冬酶3表达水平的提高,这表明细胞毒性T淋巴细胞可能引起肿瘤细胞的改变并随后诱导细胞死亡。这些结果表明,细胞毒性T淋巴细胞免疫突触的形成发生在人体组织中,并且可能与有效的免疫介导的致瘤细胞清除有关,因此为胶质母细胞瘤免疫治疗开辟了新途径。

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