通过CCR5介导,在呼吸道中维持常存记忆T细胞的动态维护
Tiange Shao1,2,3, Jiacheng Yao4,5, Shiyue Hou6,1,7
1Laboratory of Dynamic Immunobiology, Institute for Immunology, Tsinghua University, Beijing, 100084, China.
Science China. Life sciences
|June 3, 2025
概括
组织内存T细胞 (TRM) 从肺部迁移到排水淋巴结,维持呼吸道免疫力. 这种肺到淋巴结的迁移优化了CD8+T细胞的记忆和对流感感染的二次反应.
科学领域:
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
- 呼吸系统医学 呼吸系统医学
背景情况:
- 组织内存T细胞 (TRM) 对于屏障部位的免疫是至关重要的.
- 维持TRM群体的机制及其与淋巴细胞器官记忆T细胞的关系仍然不清楚.
研究的目的:
- 研究呼吸道和排水淋巴结中的病毒特异性CD8+TRM细胞的维持和迁移模式.
- 阐明控制TRM细胞在肺组织和淋巴结之间迁移的分子机制.
主要方法:
- 基于条形码的血统追踪
- 单细胞转录组分析
- 对CXCR3和CCR5/CCL5轴的功能研究.
- 内细胞转移和药物阻断 (马拉维罗克)
主要成果:
- 鉴定出一种独特的CD69+CD103+病毒特异性的CD8+ T细胞群在排水淋巴结 (dLN) 中,与肺TRM细胞具有转录学相似性.
- 证明CXCR3和CCR5-CCL5轴对于TRM细胞的肺到dLN逆向迁移至关重要.
- 表明DLN TRM细胞有助于二次反应,并可以重建肺TRM群体.
结论:
- 肺部TRM细胞逆向迁移到排水淋巴结,由CCR5-CCL5轴促进.
- 这种迁移途径对于在呼吸道中维持CD8+T细胞记忆至关重要.
- 这些发现揭示了一种优化局部T细胞记忆和对再感染的反应的新机制.
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