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抗原和转化生长因子β受体有助于记忆 CD8 T 细胞的长期功能和表型异质性。

Antigen and transforming growth factor Beta receptors contribute to long term functional and phenotypic heterogeneity of memory CD8 T cells.

机构信息

University of Connecticut Health Center , Farmington, CT , USA.

出版信息

Front Immunol. 2013 Aug 12;4:227. doi: 10.3389/fimmu.2013.00227. eCollection 2013.

Abstract

Pathogen-specific CD8 T cells provide a mechanism for selectively eliminating host cells that are harboring intracellular pathogens. The pathogens are killed when lytic molecules are injected into the cytoplasm of the infected cells and begin an apoptotic cascade. Activated CD8 T cells also release large quantities of pro-inflammatory cytokines that stimulate other immune cells in the local vicinity. As the alveoli are extraordinarily sensitive to cytokine induced damage, multiple layers of immune regulation limit the activities of immune cells that enter the lungs. These mechanisms include receptor-mediated signaling pathways in CD8 T cells that respond to peptide antigens and transforming growth factor β. Both pathways influence the functional and phenotypic properties of long-lived CD8 T cells populations in peripheral and lymphoid tissues.

摘要

病原体特异性 CD8 T 细胞为选择性消除携带细胞内病原体的宿主细胞提供了一种机制。当裂解分子注入感染细胞的细胞质并开始凋亡级联时,病原体就会被杀死。激活的 CD8 T 细胞还会释放大量促炎细胞因子,刺激附近的其他免疫细胞。由于肺泡对细胞因子诱导的损伤极其敏感,因此多层免疫调节限制了进入肺部的免疫细胞的活性。这些机制包括 CD8 T 细胞中对肽抗原和转化生长因子β作出反应的受体介导的信号通路。这两条通路都影响外周和淋巴组织中长寿 CD8 T 细胞群体的功能和表型特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f657/3740294/b1b1069b6708/fimmu-04-00227-g001.jpg

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