Biomedical Research Unit of Zacatecas-Mexican Institute of Social Security, Zacatecas, Mexico; Laboratory of Immunology, Autonomous University of San Luis Potosí, San Luis Potosi, Mexico.
Biomedical Research Unit of Zacatecas-Mexican Institute of Social Security, Zacatecas, Mexico.
Microb Pathog. 2021 Apr;153:104768. doi: 10.1016/j.micpath.2021.104768. Epub 2021 Jan 29.
Tuberculosis (TB) is the first cause of death by a single infectious agent. Previous reports have highlighted the presence of platelets within Tb granulomas, albeit the immune-associated platelet response to Mycobacterium tuberculosis (Mtb) has not been deeply studied. Our results showed that platelets are recruited into the granuloma in the late stages of tuberculosis. Furthermore, electron-microscopy studies showed that platelets can internalize Mtb and produce host defense peptides (HDPs), such as RNase 7, HBD2 and hPF-4 that bind to the internalized Mtb. Mtb-infected platelets exhibited higher transcription and secretion of IL-1β and TNF-α, whereas IL-10 and IL-6 protein levels decreased. These results suggest that platelets participate in the immune response against Mtb through HDPs and cytokines production.
结核病(TB)是单一传染病原体导致死亡的首要原因。之前的报告强调了血小板在结核肉芽肿中的存在,尽管针对结核分枝杆菌(Mtb)的免疫相关血小板反应尚未得到深入研究。我们的研究结果表明,血小板在结核病的晚期被招募到肉芽肿中。此外,电子显微镜研究表明,血小板可以内化 Mtb 并产生宿主防御肽(HDPs),如 RNase 7、HBD2 和 hPF-4,这些肽与内化的 Mtb 结合。感染 Mtb 的血小板表现出更高的转录和分泌 IL-1β 和 TNF-α,而 IL-10 和 IL-6 蛋白水平下降。这些结果表明,血小板通过 HDPs 和细胞因子的产生参与了针对 Mtb 的免疫反应。