Department of Nutrition, Shengli Oilfield Central Hospital, Dongying, Shandong, China.
Department of Nutrition, Shengli Oilfield Central Hospital, Dongying, Shandong, China.
Biochem Biophys Res Commun. 2019 Aug 27;516(3):1007-1012. doi: 10.1016/j.bbrc.2019.06.078. Epub 2019 Jul 2.
Commensal microbiota modulates the anti-tumor immune response and alters the tumor infiltration of T cells in numerous human malignancies. Moreover, the existence of commensals and microbial metabolites has been directly observed inside numerous epithelial tumors. Their effects on the host immune system, independent of the pre-existing malignancy, are not completely understood. To resolve this issue, we compared immune modulatory roles of the fecal bacteria from healthy individuals and the fecal bacteria from colorectal cancer (CRC) patients. Peripheral blood mononuclear cells that were provided by healthy donors were used as study systems. Overall, fecal bacteria could potently activate the degranulation and cytotoxicity of CD8 T cells. Interestingly, fecal bacteria from CRC patients in general induced higher degranulation and higher cytotoxicity than fecal bacteria from healthy individuals. These effects were dependent on the presence of antigen-presenting cells, such as monocytes and B cells, as fecal bacteria added directly to isolated CD8 T cells failed to induce high cytotoxicity. Additionally, fecal bacteria from CRC patients induced stronger upregulation of CD80 and NOS2 expression in monocytes than fecal bacteria from healthy individuals. On the other hand, the viability of CD8 T cells was significantly reduced with increasing levels of bacterial stimulation. Overall, we demonstrated that fecal bacteria from CRC patients could upregulate degranulation and cytotoxicity of CD8 T cells in a manner that was dependent on antigen-presenting cells, and was more proinflammatory than fecal bacteria from healthy individuals.
共生微生物调节抗肿瘤免疫反应,并改变多种人类恶性肿瘤中 T 细胞的浸润。此外,在许多上皮性肿瘤中已经直接观察到共生体和微生物代谢物的存在。它们对宿主免疫系统的影响,独立于先前存在的恶性肿瘤,尚未完全理解。为了解决这个问题,我们比较了健康个体和结直肠癌(CRC)患者粪便细菌的免疫调节作用。我们将健康供体提供的外周血单核细胞作为研究系统。总的来说,粪便细菌可以强烈激活 CD8 T 细胞的脱颗粒和细胞毒性。有趣的是,CRC 患者的粪便细菌通常比健康个体的粪便细菌诱导更高的脱颗粒和更高的细胞毒性。这些效应依赖于抗原呈递细胞的存在,如单核细胞和 B 细胞,因为直接添加到分离的 CD8 T 细胞中的粪便细菌不能诱导高细胞毒性。此外,CRC 患者的粪便细菌在单核细胞中诱导更高的 CD80 和 NOS2 表达上调,而健康个体的粪便细菌则较低。另一方面,随着细菌刺激水平的增加,CD8 T 细胞的活力显著降低。总的来说,我们证明了 CRC 患者的粪便细菌可以通过依赖抗原呈递细胞的方式上调 CD8 T 细胞的脱颗粒和细胞毒性,并且比健康个体的粪便细菌更具促炎作用。