Center for Integrated Immunology and Vaccine Research, Department of Immunology, University of Connecticut Health Center, Farmington, CT 06030, USA.
Immunity. 2013 Jul 25;39(1):184-95. doi: 10.1016/j.immuni.2013.06.015.
The study of T cell memory and the target of vaccine design have focused on memory subsumed by T cells bearing the αβ T cell receptor. Alternatively, γδ T cells are thought to provide rapid immunity, particularly at mucosal borders. Here, we have shown that a distinct subset of mucosal γδ T cells mounts an immune response to oral Listeria monocytogenes (Lm) infection and leads to the development of multifunctional memory T cells capable of simultaneously producing interferon-γ and interleukin-17A in the murine intestinal mucosa. Challenge infection with oral Lm, but not oral Salmonella or intravenous Lm, induced rapid expansion of memory γδ T cells, suggesting contextual specificity to the priming pathogen. Importantly, memory γδ T cells were able to provide enhanced protection against infection. These findings illustrate that γδ T cells play a role with hallmarks of adaptive immunity in the intestinal mucosa.
该研究的 T 细胞记忆和疫苗设计的目标集中在记忆归入 T 细胞载体的αβ T 细胞受体。或者,γδ T 细胞被认为提供快速免疫,特别是在黏膜边界。在这里,我们已经表明,一个独特的子集黏膜 γδ T 细胞装载免疫反应口服李斯特菌 (单核细胞增生李斯特菌) 感染和导致多功能记忆 T 细胞的发展能够同时产生干扰素-γ和白细胞介素-17A 在鼠肠黏膜。与口服单核细胞增生李斯特菌感染的挑战,但不是口服沙门氏菌或静脉内单核细胞增生李斯特菌,诱导记忆 γδ T 细胞的快速扩张,表明上下文特异性的启动病原体。重要的是,记忆 γδ T 细胞能够提供增强的保护免受感染。这些研究结果表明,γδ T 细胞在肠道黏膜中发挥作用的特点是适应性免疫。